Lipoedema
Epidemiologia

Lipoedema to przewlekła choroba tkanki tłuszczowej dotykająca około 10-11% dorosłych kobiet globalnie, charakteryzująca się nieproporcjonalnym gromadzeniem tkanki tłuszczowej w dolnych partiach ciała, z oszczędzeniem stóp i dłoni. Epidemiologia lipoedema jest trudna do precyzyjnego określenia z powodu błędnej diagnozy, braku specyficznych biomarkerów oraz niskiej świadomości wśród personelu medycznego. Częstość występowania w różnych krajach waha się od 6,5% do nawet 39%, a choroba manifestuje się najczęściej w okresach zmian hormonalnych, takich jak dojrzewanie (57-64% przypadków), ciąża i menopauza. Genetyczne podłoże potwierdzają dane wskazujące na dziedziczność w 20-60% przypadków oraz identyfikację SNP w pobliżu genu LHFPL6. Diagnostyka opiera się głównie na badaniu klinicznym, a nowe metody, takie jak ultrasonografia z punktem odcięcia 11,7 mm grubości tkanki podskórnej czy DXA, wykazują wysoką czułość (95-96%).

Epidemiologia Lipoedem

Lipoedema to choroba tkanki tłuszczowej, która występuje niemal wyłącznie u kobiet i charakteryzuje się nieproporcjonalnym gromadzeniem się tkanki tłuszczowej, głównie w dolnych częściach ciała, przy jednoczesnym oszczędzeniu stóp i dłoni. Dokładna częstość występowania lipoedem nie jest w pełni poznana, a dane epidemiologiczne są ograniczone, co wynika z braku wystarczających badań epidemiologicznych i trudności diagnostycznych.123

Szacunkowa częstotliwość występowania

Na podstawie dostępnych badań szacuje się, że lipoedema dotyka około 10-11% populacji dorosłych kobiet na świecie, co przekłada się na około 400 milionów kobiet.456 Jednakże w literaturze medycznej można znaleźć różne szacunki dotyczące częstości występowania tej choroby:

  • Według niektórych źródeł częstość występowania lipoedem waha się od 6,5% do 19% populacji kobiet78
  • W Stanach Zjednoczonych szacuje się, że choroba dotyka około 6,5% populacji9
  • W Niemczech wskaźniki częstości występowania wahają się od 6-8% do nawet 39% kobiet1011
  • W ośrodkach naczyniowych częstość występowania szacuje się na 15-19%12
  • W Brazylii na podstawie badań screeningowych online szacuje się, że 12,3% respondentek spełnia kryteria lipoedem, co przekłada się na około 8,8 miliona kobiet w tym kraju1314

Niektóre źródła podają znacznie niższe wskaźniki, np. 1 na 72 000 osób, jednak te dane są powszechnie uważane za znacznie zaniżone.1516 Inne badanie przeprowadzone w brytyjskim oddziale dermatologicznym odnotowało zaledwie 67 przypadków lipoedem w ciągu 15 lat, co daje minimalną szacowaną częstość występowania na poziomie 0,001%, choć autorzy podkreślają, że jest to prawdopodobnie znaczne niedoszacowanie.1718

Czynniki wpływające na rozbieżności w danych epidemiologicznych

Istnieje kilka kluczowych powodów, dla których dane epidemiologiczne dotyczące lipoedem są tak zróżnicowane i niepewne:1920

  • Błędna diagnoza i niedodiagnozowanie – lipoedema jest często mylnie diagnozowane jako otyłość, obrzęk limfatyczny lub inne formy obrzęku, co prowadzi do zaniżenia rzeczywistej częstości występowania2122
  • Brak specyficznego testu diagnostycznego – nie istnieją specyficzne biomarkery czy standardowe testy diagnostyczne dla lipoedem, a diagnoza opiera się głównie na badaniu klinicznym i wywiadzie medycznym2324
  • Niewystarczająca świadomość wśród personelu medycznego – wielu lekarzy nie jest odpowiednio przeszkolonych w rozpoznawaniu lipoedem2526
  • Brak wysokiej jakości badań epidemiologicznych – przeprowadzenie dokładnych badań epidemiologicznych wymaga znacznych zasobów finansowych i czasowych27
  • Różnice w metodologii badań – badania wykorzystują różne kryteria diagnostyczne i metody badawcze, co prowadzi do rozbieżnych wyników28

Różnice geograficzne i demograficzne

Badania sugerują, że występowanie lipoedem może różnić się w zależności od regionu geograficznego i przynależności etnicznej:29

  • W Europie szacuje się, że choroba dotyka 15-18% kobiet, ze szczególnym nasileniem u kobiet kaukaskich3031
  • W Niemczech około 10% kobiet może cierpieć na lipoedema32
  • W Azji choroba wydaje się występować znacznie rzadziej lub nie jest rozpoznawana33
  • U kobiet pochodzenia afrykańskiego lipoedema często rozwija się w specyficznej formie, dotykając głównie obszaru bioder i pośladków34

Charakterystyka demograficzna pacjentów

Lipoedema występuje przede wszystkim u kobiet, a przypadki u mężczyzn są niezwykle rzadkie.3536 Warto podkreślić, że choroba ta ma kilka charakterystycznych cech demograficznych:

Występowanie w grupach wiekowych

Lipoedema najczęściej pojawia się w okresach zmian hormonalnych u kobiet:3738

  • Okres dojrzewania – u wielu pacjentek pierwsze objawy pojawiają się w okresie pokwitania (57-64% przypadków)39
  • Ciąża – niektóre pacjentki doświadczają początku choroby lub jej nasilenia podczas ciąży40
  • Menopauza – u części kobiet choroba rozwija się lub ulega zaostrzeniu w okresie menopauzy41

Badanie przeprowadzone wśród 209 pacjentek z lipoedema wykazało, że objawy typowo pojawiają się około 16 roku życia. W innym badaniu stwierdzono, że 70% kobiet z lipoedema doświadczyło początku choroby przed 30 rokiem życia, jednak tylko 1,6% zostało wcześniej zdiagnozowanych przez pracownika służby zdrowia.42

Predyspozycje genetyczne i rodzinne

Istnieją wyraźne dowody na genetyczne podłoże choroby:43

  • W 20-60% przypadków choroba występuje rodzinnie, co sugeruje dziedziczny charakter44
  • Około połowa pacjentek zgłasza występowanie podobnych objawów u członków rodziny45
  • Badania wskazują na dziedziczność na poziomie 50-60%, co potwierdza silny związek genetyczny z lipoedema46
  • Badacze zidentyfikowali kilka potencjalnych regionów genomu związanych z chorobą, w tym SNP w pobliżu genu LHFPL647

Wyzwania w monitorowaniu i nadzorze epidemiologicznym

Monitorowanie i nadzór epidemiologiczny nad lipoedema napotyka na szereg trudności, które utrudniają ustalenie dokładnego rozpowszechnienia choroby i opracowanie skutecznych strategii zdrowia publicznego.4849

Problemy diagnostyczne

Główne wyzwania w diagnozowaniu lipoedema to:5051

  • Brak specyficznych biomarkerów – obecnie nie istnieją specyficzne biomarkery pozwalające na jednoznaczne potwierdzenie diagnozy52
  • Subiektywna ocena kliniczna – diagnoza opiera się głównie na dokładnym wywiadzie medycznym i kompleksowym badaniu fizykalnym obejmującym inspekcję i palpację53
  • Nakładanie się objawów z innymi chorobami – objawy lipoedema mogą przypominać otyłość, obrzęk limfatyczny lub inne schorzenia5455
  • Niedostateczna wiedza wśród personelu medycznego – wielu lekarzy nie jest odpowiednio przeszkolonych w rozpoznawaniu lipoedema56

Naukowcy pracują nad nowymi metodami diagnostycznymi, które mogłyby pomóc w bardziej obiektywnym rozpoznawaniu choroby:57

  • Badanie ultrasonograficzne – brazylijska praca zaproponowała punkt odcięcia 11,7 mm grubości tkanki podskórnej w okolicy przedgoleniowej, osiągając 96% swoistość diagnostyczną58
  • Absorpcjometria rentgenowska o podwójnej energii (DXA) – wykazała 95% czułość w diagnozowaniu lipoedema59
  • Biomarker Pf4 (czynnik płytkowy 4) – badania wskazują, że jest on podwyższony w egzosomach pochodzących z osocza u pacjentek z lipoedema, co może stanowić potencjalny marker diagnostyczny6061

Opóźniona diagnoza

Jednym z największych wyzwań w nadzorze epidemiologicznym jest znaczne opóźnienie w diagnozowaniu lipoedema:6263

  • Badanie przeprowadzone przez Lipoedema UK (2021) wykazało, że 57% respondentek doświadczyło objawów w okresie dojrzewania, ale tylko 2% otrzymało diagnozę w tym czasie64
  • Aż 62% badanych otrzymało diagnozę dopiero w późniejszym okresie życia (między 41 a 80 rokiem życia)65
  • Średni czas do postawienia diagnozy wynosi około 15 lat66
  • Wiele kobiet żyje z objawami lipoedema i niepewnością co do swojego stanu zdrowia przez dekady, zanim zostaną prawidłowo zdiagnozowane67

Opóźniona diagnoza prowadzi do progresji choroby, komplikacji i pogorszenia jakości życia pacjentek, co dodatkowo utrudnia gromadzenie dokładnych danych epidemiologicznych.68

Trudności w gromadzeniu danych

Dokładne określenie epidemiologii lipoedema napotyka na następujące przeszkody:6970

  • Wysokie koszty badań epidemiologicznych – wysokiej jakości badania epidemiologiczne wymagają znacznych zasobów finansowych i czasowych71
  • Brak standardowych narzędzi screeningowych – nie ma powszechnie przyjętych, zwalidowanych narzędzi do badań przesiewowych na dużą skalę72
  • Różnice w kryteriach diagnostycznych – badania wykorzystują różne kryteria i definicje, co utrudnia porównywanie wyników73
  • Stygmatyzacja i ukrywanie choroby – pacjentki mogą nie zgłaszać się do lekarza z powodu stygmatyzacji związanej z wyglądem74
  • Ograniczony dostęp do opieki specjalistycznej – w wielu regionach nie ma specjalistycznych klinik zajmujących się lipoedema75

Wpływ na zdrowie publiczne

Lipoedema ma znaczący wpływ na zdrowie publiczne, co podkreśla potrzebę lepszego monitorowania epidemiologicznego tej choroby.7677

Obciążenie systemów opieki zdrowotnej

Lipoedema generuje znaczne koszty dla systemów opieki zdrowotnej:7879

  • Koszty wielokrotnych konsultacji – pacjentki często konsultują się z wieloma specjalistami przed uzyskaniem właściwej diagnozy80
  • Koszty leczenia chorób współistniejących – lipoedema wiąże się z wieloma chorobami współistniejącymi, które wymagają dodatkowego leczenia81
  • Koszty leczenia chirurgicznego – zabiegi liposukcji, które są najskuteczniejszą metodą leczenia, są kosztowne i często nie są pokrywane przez ubezpieczenie8283
  • Koszty terapii zachowawczejkompleksowa terapia przeciwzastoinowa, kompresjoterapia i fizjoterapia generują długoterminowe koszty84

Dokładne dane dotyczące ekonomicznego obciążenia związanego z lipoedema są trudne do oszacowania ze względu na ograniczone dane epidemiologiczne.8586

Wpływ na jakość życia pacjentek

Lipoedema ma znaczący wpływ na jakość życia kobiet:8788

  • Ból i dyskomfort fizyczny – głównym objawem lipoedem jest ból, który może znacząco ograniczać codzienne funkcjonowanie8990
  • Ograniczenia w aktywności fizycznej – pacjentki często doświadczają trudności w poruszaniu się i wykonywaniu ćwiczeń91
  • Wpływ na zdrowie psychiczne – około 85% pacjentek zgłasza, że lipoedema wpływa na ich zdrowie psychiczne i zdolność radzenia sobie z życiem92
  • Stygmatyzacja społeczna – kobiety z lipoedema często doświadczają stygmatyzacji i są błędnie postrzegane jako osoby z otyłością wynikającą z nieodpowiedniego stylu życia9394
  • Wpływ na zatrudnienie – choroba może ograniczać zdolność do pracy i rozwoju zawodowego95

Badania wykazały, że kobiety z lipoedema zgłaszają znacząco niższą jakość życia związaną ze zdrowiem (HRQOL) w porównaniu z ogólną populacją kobiet.96

Znaczenie wczesnej diagnozy

Wczesna diagnoza lipoedema ma kluczowe znaczenie dla lepszego zarządzania chorobą i poprawy jakości życia pacjentek:9798

  • Spowolnienie progresji choroby – wczesne wdrożenie odpowiedniego leczenia może spowolnić postęp choroby99
  • Zmniejszenie ryzyka powikłań – odpowiednie leczenie może zapobiec rozwojowi wtórnego obrzęku limfatycznego i innych powikłań100
  • Poprawa zarządzania objawami – wczesne wdrożenie strategii zarządzania objawami może zmniejszyć ból i dyskomfort101
  • Wsparcie psychologiczne – wczesna diagnoza umożliwia zapewnienie odpowiedniego wsparcia psychologicznego102
  • Edukacja pacjenta – zrozumienie choroby pomaga pacjentkom w aktywnym zarządzaniu swoim stanem103

Niestety, badania wskazują na poważne braki w wykrywaniu lipoedema we wczesnych stadiach, co sugeruje, że wiele kobiet jest zmuszonych radzić sobie z problemami zdrowotnymi bez odpowiedniego wsparcia ze strony służby zdrowia.104

Przyszłe kierunki badań epidemiologicznych

Aby lepiej zrozumieć epidemiologię lipoedema i poprawić opiekę nad pacjentkami, konieczne są dalsze badania w kilku kluczowych obszarach.105106

Potrzeby badawcze

Priorytetowe obszary badań epidemiologicznych obejmują:107108

  • Systematyczne badania populacyjne – potrzebne są duże, wieloośrodkowe badania z jasno określonymi kryteriami diagnostycznymi109
  • Standaryzacja kryteriów diagnostycznych – opracowanie i walidacja jednolitych kryteriów diagnostycznych dla badań epidemiologicznych110
  • Badania biomarkerów – identyfikacja i walidacja biomarkerów diagnostycznych dla lipoedema111112
  • Badania genetyczne – dalsze badania nad podłożem genetycznym lipoedema113114
  • Badania międzykulturowe – zbadanie różnic w częstości występowania i manifestacji choroby w różnych populacjach115

Innowacyjne podejścia do badania epidemiologii

Ze względu na wysokie koszty tradycyjnych badań epidemiologicznych, potrzebne są innowacyjne podejścia do zbierania danych:116117

  • Wykorzystanie rejestrów medycznych – analiza danych z elektronicznych rejestrów medycznych może dostarczyć cennych informacji epidemiologicznych118
  • Badania online – dobrze zaprojektowane narzędzia screeningowe online mogą pomóc w zbieraniu danych od dużej liczby osób119120
  • Metody analizy danych – zaawansowane metody analizy danych i sztuczna inteligencja mogą pomóc w identyfikacji wzorców i trendów121
  • Współpraca międzynarodowa – koordynacja wysiłków badawczych na poziomie międzynarodowym może prowadzić do bardziej kompleksowych i porównywalnych danych122

Zmiana terminologii i koncepcji choroby

W ostatnich latach pojawiły się propozycje zmiany terminologii używanej do opisania lipoedema, co może wpłynąć na przyszłe badania epidemiologiczne:123124

  • Termin „lipoedema” uznawany za mylący – badania z wykorzystaniem ultrasonografii wysokiej rozdzielczości nie wykazały obecności płynu w tkance miękkiej nóg u pacjentek z lipoedema125
  • Propozycja nowej nazwy – zaproponowano termin „zespół lipalgii” (lipalgia syndrome), który lepiej odzwierciedla główny objaw choroby – ból związany z tkanką tłuszczową126127
  • Zmiana podejścia terapeutycznego – zmiana koncepcji choroby może prowadzić do bardziej odpowiedniego podejścia terapeutycznego, skupiającego się na leczeniu bólu i przewlekłego stanu zapalnego, a nie na terapii przeciwobrzękowej128129

Te zmiany w postrzeganiu lipoedema mogą wpłynąć na sposób, w jaki choroba jest klasyfikowana i monitorowana w przyszłych badaniach epidemiologicznych.130

Znaczenie dokładnych danych epidemiologicznych

Dokładne dane dotyczące częstości występowania lipoedema mają kluczowe znaczenie z wielu powodów:131132

  • Uzasadnienie finansowania badań – dokładne dane mogą pomóc przekonać instytucje finansujące i decydentów o znaczeniu badań nad lipoedema133
  • Planowanie zasobów opieki zdrowotnej – pozwala na lepsze planowanie zasobów i usług specjalistycznych134
  • Rozwój programów edukacyjnych – pomaga w ukierunkowaniu programów edukacyjnych dla pracowników służby zdrowia135
  • Opracowanie strategii zdrowia publicznego – umożliwia tworzenie skutecznych strategii prewencji i wczesnej interwencji136
  • Zwiększenie świadomości społecznej – dokładne dane mogą pomóc w zwiększeniu świadomości społecznej na temat choroby137

Lepsze zrozumienie epidemiologii lipoedema może pomóc zmniejszyć opóźnienia w diagnostyce, poprawić dostęp do specjalistycznej opieki i zapobiec potencjalnemu niedodiagnozowaniu.138

Podsumowanie stanu wiedzy epidemiologicznej

Pomimo rosnącego zainteresowania lipoedema w ostatnich latach, nasza wiedza na temat epidemiologii tej choroby pozostaje ograniczona.139140 Najczęściej cytowane dane wskazują, że choroba dotyka około 10-11% populacji dorosłych kobiet, jednak rzeczywista częstość występowania może się znacznie różnić w zależności od regionu geograficznego, populacji i metodologii badań.141142

Główne wyzwania w dokładnym określeniu epidemiologii lipoedema obejmują trudności diagnostyczne, niewystarczającą świadomość choroby wśród pracowników służby zdrowia, brak standardowych narzędzi diagnostycznych oraz wysokie koszty badań epidemiologicznych.143144

Potrzebne są dalsze badania, aby lepiej zrozumieć rozpowszechnienie lipoedema w różnych populacjach, zidentyfikować czynniki ryzyka, opracować skuteczne strategie prewencji i poprawić opiekę nad pacjentkami.145146 Dokładniejsze dane epidemiologiczne mogą pomóc w zwiększeniu świadomości na temat tej choroby, poprawie dostępu do opieki i opracowaniu skuteczniejszych strategii leczenia.147148

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  1. 11.04.2026
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Materiały źródłowe

  • #1 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #2 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    Lipedema, a malady that is not well-understood, can detrimentally affect ones quality of life, ability to work, and healthcare costs. […] Despite the far-reaching effects of Lipedema and its potentially high rate of occurrence, there is still very little information about how many populations it affects, how often it interferes with peoples lives, and the accurate price of its healthcare. […] The lack of information on Lipedema is due to the lack of epidemiological studies. […] Accurate prevalence figures for Lipedema are essential to best address the issue. Without precise data, efforts to combat this condition are severely hindered. […] The majority of estimates highlight that Lipedema is not a rare condition. […] The exact Lipedema prevalence is uncertain, though a 2020 literature review suggests that 10-11% of women, or approximately 400 million people, have it.
  • #3 About Lipedema — Lipedema Foundation
    https://www.lipedema.org/about-lipedema
    Lipedema is a chronic condition that occurs almost exclusively in women and manifests as symmetrical buildup of often-painful fat in the limbs, sparing the hands and feet. […] As a result, the true number of women with Lipedema, or its epidemiology, is unknown. […] In 2023, the Lipedema Foundation published the Research Roadmap. The Roadmap identifies recommendations to strengthen and expand Lipedema research, enhance knowledge, reduce barriers, facilitate exchange of ideas, and advance best practices.
  • #4 Lipedema: A Relatively Common Disease with Extremely Common Misconceptions
    https://pmc.ncbi.nlm.nih.gov/articles/PMC5055019/
    Lipedema, or adiposis dolorosa, is a common adipose tissue disorder that is believed to affect nearly 11% of adult women worldwide. […] With an incidence that may affect nearly 1 in 9 adult women, it is important to generate appropriate awareness, conduct additional research, and identify better diagnostic and treatment modalities for lipedema so these women can obtain the care that they need and deserve. […] If estimates are correct, lipedema may affect millions of women in the United States alone, with an estimated incidence of 1 in 9 adult women. […] Despite its description in 1940 by Allen and Hines, little is understood about the adipose tissue disorder, lipedema. […] One of the greatest difficulties with treatment of lipedema is insurance coverage for the surgical treatment. […] With an incidence that may affect nearly 1 in 9 adult women, it is important to generate appropriate awareness, conduct additional research, and identify better diagnostic and treatment modalities so these women can obtain the care that they need and deserve.
  • #5 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    Lipedema, a poorly understood disease characterized by irregular fat distribution and accumulation, can dramatically impact quality of life, workforce participation, and healthcare costs. […] Yet despite Lipedemas impacts and a high estimated prevalence of the disease, we know little about how frequently it manifests in different populations, how regularly symptoms disrupt daily life, or its precise healthcare costs. […] Accurate and innovative prevalence data is necessary to understand the true dimensions and impacts of Lipedema. […] A literature review published in 2020 estimated that 10-11% of womensome 400 million peoplehave Lipedema. […] One British dermatology department documented 67 Lipedema cases in 15 years, resulting in a minimum prevalence estimate of 0.001% although the authors noted this is likely an underestimate.
  • #6 Lipedema – The Disease They Call FAT – Lipedema Project
    https://lipedemaproject.org/ebook/
    Lipedema The Disease They Call FAT: An Overview for Clinicians is a monograph that provides a clinical synopsis of this condition. This monograph covers the history of lipedema and includes sections on epidemiology, etiology, pathogenesis, clinical features, diagnosis and how to differentiate between lipedema and other disorders, such as lymphedema and obesity. […] Estimates of the incidence of lipedema range as high as 11% of the post-pubertal female population, which is approximately 17 million women in the United States alone. […] Research and clinical communities have a long way to go toward appropriately recognizing, diagnosing, and understanding this disease.
  • #7 Observational Study on a Large Italian Population with Lipedema: Biochemical and Hormonal Profile, Anatomical and Clinical Evaluation, Self-Reported History
    https://www.mdpi.com/1422-0067/25/3/1599
    We analyzed the medical condition of 360 women affected by lipedema of the lower limbs in stages 1, 2, and 3. […] The true prevalence of lipedema is unknown, although it is thought to be a common disease. The estimated prevalence ranges from 6.5% in children in the United States and 6–8% in women in Germany to 15–19% in vascular disease clinics. […] The diagnosis of lipedema is clinical and is carried out through the evaluation of diagnostic criteria helpful in framing the characteristics of the pathological tissue. […] The standard conservative therapy for lipedema includes specific physiotherapy and nutritional treatments, compression garments, and specific motor physical activity plans. […] This study aimed to analyze the medical history and the clinical, ultrasound, and laboratory characteristics of a large number of Italian women affected by lipedema. No previous study has reported data on Italian women affected by lipedema.
  • #8 Assessment of lipoedema awareness among polish women- online survey study | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-023-02614-7
    According to the present knowledge, lipoedema is a chronic disease and it cannot be fully cured through a conservative approach. […] The exact prevalence remains unknown however various data provide estimated values varying from 7 to 19% of the female population. […] Overall knowledge of lipoedema in our study was low as the correct definition of lipoedema was indicated by 7% of women, and 4%, 12%, and 37% could mark the correct methods of treatment, clinical features, and durability of lipoedema respectively. […] Our research may help spread knowledge about lipoedema both among medical professionals and the general population, which could have an impact on decreasing the number of undiagnosed cases.
  • #9 Lipoedema – is a paradigm shift needed? | CarEdOn
    https://www.caredon.org/blog/lipoedema-paradigm-shift-needed
    Lipoedema is a chronic condition in women characterized by a disproportionate increase in adipose tissue in the legs (sometimes in the arms) together with pain (or/and tender to touch the skin) in this adipose tissue. […] Research on lipoedema is scarce, and clear diagnostic tools are lacking. This contributes to the fact that the prevalence rate of lipoedema is largely unknown. In a recently published US lipoedema guideline, it was stated that prevalence estimates range from 6.5% in children in the US, 6%-8% in women in Germany, and 15%-19% in vascular clinics. […] Consequently, purely lipoedema does not include oedema, neither is there any scientific evidence for lymphatic insufficiency. Therefore, decongestive lymphatic treatment is inappropriate for patients with purely lipoedema. […] Up to now, a chronic low-grade state of inflammation and tissue hypoxia are the most plausible explanations for the pain experienced in lipoedema patients.
  • #10 SciELO Brazil – Lipedema: exploring pathophysiology and treatment strategies – state of the art Lipedema: exploring pathophysiology and treatment strategies – state of the art
    https://www.scielo.br/j/jvb/a/VtfxqW3hknsDFw8BGFPfTTb/
    Lipedema is characterized by abnormal fat deposition in areas such as the arms, hips, buttocks, and thighs, sparing the hands and feet. […] Prevalence in the general population varies from 0.06% to 1011%, reaching higher rates in some countries, such as Germany, where it affects up to 39% of women. In Brazil, the prevalence of lipedema is estimated to be 12.3% among Brazilian women. With approximately 100.5 million women in Brazil in 2021, it can be predicted that 8.8 million of them may have symptoms suggestive of lipedema. […] In recent years, lipedema has gained recognition among both healthcare professionals and the general population. This increased visibility is attributable to online dissemination of information and growing medical attention devoted to this condition. However, comprehensive knowledge of lipedema, including its pathophysiology, clinical aspects, and conservative and surgical treatment modalities, is not yet fully consolidated in the healthcare field.
  • #11 SciELO Brazil – Prevalência e fatores de risco para lipedema no Brasil Prevalência e fatores de risco para lipedema no Brasil
    https://www.scielo.br/j/jvb/a/Q9yR3XdzXVbrsB37KQD3mfg/?lang=en
    Lipedema is characterized as an abnormal deposition of fat in the buttocks and legs bilaterally that may be accompanied by swelling, pain, and tenderness. The estimated prevalence in Europe varies between 0.06% and 39%. […] The estimated prevalence of lipedema in the population of Brazilian women is 12.3%. […] The literature reports estimated prevalence rates of lipedema in the German population ranging from 0.06% to 39%. […] The most widely-accepted lipedema prevalence reported in the literature was estimated by Fldi and Fldi, who extrapolated their clinical experience to the general population, estimating that up to 11% of the female population may have lipedema. […] According to Schwahn-Schreiber and Marshall, the prevalence in Germany of all stages of lipedema is as great as 39% of the population. […] We estimate, conservatively, that 8.8 million adult Brazilian women aged 18 to 69 years may have symptoms suggestive of a diagnosis of lipedema.
  • #12 Observational Study on a Large Italian Population with Lipedema: Biochemical and Hormonal Profile, Anatomical and Clinical Evaluation, Self-Reported History
    https://www.mdpi.com/1422-0067/25/3/1599
    We analyzed the medical condition of 360 women affected by lipedema of the lower limbs in stages 1, 2, and 3. […] The true prevalence of lipedema is unknown, although it is thought to be a common disease. The estimated prevalence ranges from 6.5% in children in the United States and 6–8% in women in Germany to 15–19% in vascular disease clinics. […] The diagnosis of lipedema is clinical and is carried out through the evaluation of diagnostic criteria helpful in framing the characteristics of the pathological tissue. […] The standard conservative therapy for lipedema includes specific physiotherapy and nutritional treatments, compression garments, and specific motor physical activity plans. […] This study aimed to analyze the medical history and the clinical, ultrasound, and laboratory characteristics of a large number of Italian women affected by lipedema. No previous study has reported data on Italian women affected by lipedema.
  • #13 SciELO Brazil – Prevalência e fatores de risco para lipedema no Brasil Prevalência e fatores de risco para lipedema no Brasil
    https://www.scielo.br/j/jvb/a/Q9yR3XdzXVbrsB37KQD3mfg/?lang=en
    Lipedema is characterized as an abnormal deposition of fat in the buttocks and legs bilaterally that may be accompanied by swelling, pain, and tenderness. The estimated prevalence in Europe varies between 0.06% and 39%. […] The estimated prevalence of lipedema in the population of Brazilian women is 12.3%. […] The literature reports estimated prevalence rates of lipedema in the German population ranging from 0.06% to 39%. […] The most widely-accepted lipedema prevalence reported in the literature was estimated by Fldi and Fldi, who extrapolated their clinical experience to the general population, estimating that up to 11% of the female population may have lipedema. […] According to Schwahn-Schreiber and Marshall, the prevalence in Germany of all stages of lipedema is as great as 39% of the population. […] We estimate, conservatively, that 8.8 million adult Brazilian women aged 18 to 69 years may have symptoms suggestive of a diagnosis of lipedema.
  • #14 SciELO Brazil – Lipedema: exploring pathophysiology and treatment strategies – state of the art Lipedema: exploring pathophysiology and treatment strategies – state of the art
    https://www.scielo.br/j/jvb/a/VtfxqW3hknsDFw8BGFPfTTb/
    Lipedema is characterized by abnormal fat deposition in areas such as the arms, hips, buttocks, and thighs, sparing the hands and feet. […] Prevalence in the general population varies from 0.06% to 1011%, reaching higher rates in some countries, such as Germany, where it affects up to 39% of women. In Brazil, the prevalence of lipedema is estimated to be 12.3% among Brazilian women. With approximately 100.5 million women in Brazil in 2021, it can be predicted that 8.8 million of them may have symptoms suggestive of lipedema. […] In recent years, lipedema has gained recognition among both healthcare professionals and the general population. This increased visibility is attributable to online dissemination of information and growing medical attention devoted to this condition. However, comprehensive knowledge of lipedema, including its pathophysiology, clinical aspects, and conservative and surgical treatment modalities, is not yet fully consolidated in the healthcare field.
  • #15 Lipedema – StatPearls – NCBI Bookshelf
    https://www.ncbi.nlm.nih.gov/books/NBK573066/
    It is proposed that the prevalence of lipedema is nearly 1 in 72000 population. […] Lipedema is often misdiagnosed or underdiagnosed, so these prevalence numbers are likely to be underestimated numbers. […] Lipedema occurs predominantly in females but has been reported rarely in males. […] Few reports mentioned the prevalence of lipedema around 11% in adults and around 6.5% in the US, ranging from 15% to 18% in European countries.
  • #16 Lipedema: Causes, Symptoms & Treatment
    https://my.clevelandclinic.org/health/diseases/17175-lipedema
    Lipedema causes abnormal fat buildup in your lower body, getting worse over time. […] Researchers estimate that 1 in 72,000 people have lipedema. But this number is probably low because lipedema can look like obesity or lymphedema. Another global estimate says 11% of females have lipedema. The condition is rare in males. […] The exact cause of lipedema is unknown. But the condition runs in families in 20% to 60% of cases, so you may inherit it. The condition occurs almost exclusively in women. […] You’re more likely to get lipedema if you: Being female. Have a family history of lipedema. Have a BMI higher than 35. […] Lipedema slowly worsens with time in many people. […] Early diagnosis and treatment may help you avoid complications. Exercising and using compression stockings can give you a better outcome. Liposuction can help you feel better.
  • #17 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    Lipedema, a poorly understood disease characterized by irregular fat distribution and accumulation, can dramatically impact quality of life, workforce participation, and healthcare costs. […] Yet despite Lipedemas impacts and a high estimated prevalence of the disease, we know little about how frequently it manifests in different populations, how regularly symptoms disrupt daily life, or its precise healthcare costs. […] Accurate and innovative prevalence data is necessary to understand the true dimensions and impacts of Lipedema. […] A literature review published in 2020 estimated that 10-11% of womensome 400 million peoplehave Lipedema. […] One British dermatology department documented 67 Lipedema cases in 15 years, resulting in a minimum prevalence estimate of 0.001% although the authors noted this is likely an underestimate.
  • #18 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    However, the studies used in this review are based mainly on European populations, which could skew the overall picture. […] A British dermatology department documented 67 Lipedema cases over 15 years, yielding a minimum prevalence of 0.001%. […] An online screening tool in Brazil showed that 12.3% of respondents met the Lipedema criteria, while a Germany screening found that 4.8-9.7% had moderate to severe Lipedema. […] This means Lipedema is relatively common in women. […] While Lipedema occurs almost exclusively in women, Lipedemas precise prevalence is uncertain. […] This knowledge gap is mainly due to inadequate studies of epidemiology. […] The economic effects of Lipedema are not well known due to a lack of prevalence data. […] To understand the financial burden Lipedema patients face in terms of healthcare and employment, a more precise picture of the associated costs must be established. […] Obtaining accurate information on the frequency of Lipedema continues to be a difficult endeavor due to the significant financial and temporal expenditure required for conducting quality epidemiological research.
  • #19 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #20 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    Lipedema, a malady that is not well-understood, can detrimentally affect ones quality of life, ability to work, and healthcare costs. […] Despite the far-reaching effects of Lipedema and its potentially high rate of occurrence, there is still very little information about how many populations it affects, how often it interferes with peoples lives, and the accurate price of its healthcare. […] The lack of information on Lipedema is due to the lack of epidemiological studies. […] Accurate prevalence figures for Lipedema are essential to best address the issue. Without precise data, efforts to combat this condition are severely hindered. […] The majority of estimates highlight that Lipedema is not a rare condition. […] The exact Lipedema prevalence is uncertain, though a 2020 literature review suggests that 10-11% of women, or approximately 400 million people, have it.
  • #21 Lipedema – StatPearls – NCBI Bookshelf
    https://www.ncbi.nlm.nih.gov/books/NBK573066/
    It is proposed that the prevalence of lipedema is nearly 1 in 72000 population. […] Lipedema is often misdiagnosed or underdiagnosed, so these prevalence numbers are likely to be underestimated numbers. […] Lipedema occurs predominantly in females but has been reported rarely in males. […] Few reports mentioned the prevalence of lipedema around 11% in adults and around 6.5% in the US, ranging from 15% to 18% in European countries.
  • #22 Lipedema – Wikipedia
    https://en.wikipedia.org/wiki/Lipedema
    According to an epidemiologic study by Fldi E and Fldi M, lipedema affects 11% of the female population, although rates from 6-39% have also been reported. […] Lipedema is often underdiagnosed due to the difficulty in differentiating it from lymphedema, obesity, or other edemas.
  • #23 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    Lipoedema is a chronic disease in adipose tissue that almost exclusively affects women during periods of hormonal alterations. Its main symptoms include an abnormal accumulation of subcutaneous fat in the buttock, hips, and legs, which is associated with pain, swelling, and easy bruising. […] Overall, research on lipoedema is scarce. As such, this study examined the health, health-related quality of life (HRQOL), and sense of coherence (SOC) among women with lipoedema. […] However, previous studies have revealed that lipoedema may affect approximately 10% of the female population. […] Currently, no specific biomarkers for diagnosing lipoedema are available, with it being confirmed solely through the use of a thorough medical history-taking and a comprehensive physical examination that includes both inspection and palpation.
  • #24 Diagnosis and management of lipedema – UpToDate
    https://www.uptodate.com/contents/diagnosis-and-management-of-lipedema
    Lipedema is defined by an International Consensus as „a chronic condition characterized by a disproportionate increase in adipose tissue and pain in the lower extremities, and sometimes, the upper extremities of females.” […] The true incidence of lipedema is unknown. Patients with lipedema were historically erroneously diagnosed with lymphedema and referred to lymphedema programs. Two studies reported that 4 percent of individuals referred with primary „lymphedema” actually had lipedema. […] Lipedema is a chronic condition with symmetric deposition of subcutaneous adipose tissue disproportionately in primarily the lower extremities. […] Because of the association with pain, International Consensus Guidelines have recommended renaming the disorder „lipalgia syndrome.”
  • #25 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    The leading symptom of lipoedema is pain. Other common symptoms include numbness, easy bruising, fatigue, muscle weakness, and feeling generally swollen. […] A study focusing on the psychological status and quality of life of people with lipoedema found that those with higher symptom severity reported lower levels of HRQOL. […] Women with lipoedema often describe experiences of unhelpful and misguided advice from healthcare professionals, resulting in them struggling to, by themselves, gather information in order to understand and manage their health problems. […] This study found that comorbidities among the participants were common. […] The fact that lipoedema is associated with diverse and multiple comorbidities has also been presented in previous studies. […] This study found that women with lipoedema reported a significantly lower HRQOL than does the general female population.
  • #26 How Nurses Can Spot and Support Patients Suffering from Lipedema – Minority Nurse
    https://minoritynurse.com/how-nurses-can-spot-and-support-patients-suffering-from-lipedema/
    Despite being first identified in medical literature in the 1940s and impacting 5-12% of women annually, medical professionals rarely diagnose Lipedema due to the lack of training and awareness to recognize the disease. […] Though comprehensive epidemiology data is lacking, Lipedema impacts 5-12% of women. […] Lipedema is progressive if left untreated, and is common but misdiagnosed and underrecognized. This condition carries psychological morbidity.
  • #27 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #28 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    However, the studies used in this review are based mainly on European populations, which could skew the overall picture. […] A British dermatology department documented 67 Lipedema cases over 15 years, yielding a minimum prevalence of 0.001%. […] An online screening tool in Brazil showed that 12.3% of respondents met the Lipedema criteria, while a Germany screening found that 4.8-9.7% had moderate to severe Lipedema. […] This means Lipedema is relatively common in women. […] While Lipedema occurs almost exclusively in women, Lipedemas precise prevalence is uncertain. […] This knowledge gap is mainly due to inadequate studies of epidemiology. […] The economic effects of Lipedema are not well known due to a lack of prevalence data. […] To understand the financial burden Lipedema patients face in terms of healthcare and employment, a more precise picture of the associated costs must be established. […] Obtaining accurate information on the frequency of Lipedema continues to be a difficult endeavor due to the significant financial and temporal expenditure required for conducting quality epidemiological research.
  • #29
    https://www.dw.com/en/lipedema-has-nothing-to-do-with-obesity-or-a-poor-diet/a-64286432
    Epidemiological studies do not yet exist, meaning it is difficult to know exactly how many women are affected. Estimates put it at around 370 million worldwide. Experts think there are differences in how lipedema manifests around the world. […] In Germany, probably one in ten women suffers from it. In general, Caucasian women in Europe are particularly affected. In Asia, on the other hand, lipedema is not known at all. There is a special form in African women they tend to develop lipedema in the hip area and above the rump. There it occurs more frequently in the form of painful so-called breech fat.
  • #30 Lipedema – StatPearls – NCBI Bookshelf
    https://www.ncbi.nlm.nih.gov/books/NBK573066/
    It is proposed that the prevalence of lipedema is nearly 1 in 72000 population. […] Lipedema is often misdiagnosed or underdiagnosed, so these prevalence numbers are likely to be underestimated numbers. […] Lipedema occurs predominantly in females but has been reported rarely in males. […] Few reports mentioned the prevalence of lipedema around 11% in adults and around 6.5% in the US, ranging from 15% to 18% in European countries.
  • #31
    https://www.dw.com/en/lipedema-has-nothing-to-do-with-obesity-or-a-poor-diet/a-64286432
    Epidemiological studies do not yet exist, meaning it is difficult to know exactly how many women are affected. Estimates put it at around 370 million worldwide. Experts think there are differences in how lipedema manifests around the world. […] In Germany, probably one in ten women suffers from it. In general, Caucasian women in Europe are particularly affected. In Asia, on the other hand, lipedema is not known at all. There is a special form in African women they tend to develop lipedema in the hip area and above the rump. There it occurs more frequently in the form of painful so-called breech fat.
  • #32
    https://www.dw.com/en/lipedema-has-nothing-to-do-with-obesity-or-a-poor-diet/a-64286432
    Epidemiological studies do not yet exist, meaning it is difficult to know exactly how many women are affected. Estimates put it at around 370 million worldwide. Experts think there are differences in how lipedema manifests around the world. […] In Germany, probably one in ten women suffers from it. In general, Caucasian women in Europe are particularly affected. In Asia, on the other hand, lipedema is not known at all. There is a special form in African women they tend to develop lipedema in the hip area and above the rump. There it occurs more frequently in the form of painful so-called breech fat.
  • #33
    https://www.dw.com/en/lipedema-has-nothing-to-do-with-obesity-or-a-poor-diet/a-64286432
    Epidemiological studies do not yet exist, meaning it is difficult to know exactly how many women are affected. Estimates put it at around 370 million worldwide. Experts think there are differences in how lipedema manifests around the world. […] In Germany, probably one in ten women suffers from it. In general, Caucasian women in Europe are particularly affected. In Asia, on the other hand, lipedema is not known at all. There is a special form in African women they tend to develop lipedema in the hip area and above the rump. There it occurs more frequently in the form of painful so-called breech fat.
  • #34
    https://www.dw.com/en/lipedema-has-nothing-to-do-with-obesity-or-a-poor-diet/a-64286432
    Epidemiological studies do not yet exist, meaning it is difficult to know exactly how many women are affected. Estimates put it at around 370 million worldwide. Experts think there are differences in how lipedema manifests around the world. […] In Germany, probably one in ten women suffers from it. In general, Caucasian women in Europe are particularly affected. In Asia, on the other hand, lipedema is not known at all. There is a special form in African women they tend to develop lipedema in the hip area and above the rump. There it occurs more frequently in the form of painful so-called breech fat.
  • #35 Lipedema – StatPearls – NCBI Bookshelf
    https://www.ncbi.nlm.nih.gov/books/NBK573066/
    It is proposed that the prevalence of lipedema is nearly 1 in 72000 population. […] Lipedema is often misdiagnosed or underdiagnosed, so these prevalence numbers are likely to be underestimated numbers. […] Lipedema occurs predominantly in females but has been reported rarely in males. […] Few reports mentioned the prevalence of lipedema around 11% in adults and around 6.5% in the US, ranging from 15% to 18% in European countries.
  • #36 Lipedema: Causes, Symptoms & Treatment
    https://my.clevelandclinic.org/health/diseases/17175-lipedema
    Lipedema causes abnormal fat buildup in your lower body, getting worse over time. […] Researchers estimate that 1 in 72,000 people have lipedema. But this number is probably low because lipedema can look like obesity or lymphedema. Another global estimate says 11% of females have lipedema. The condition is rare in males. […] The exact cause of lipedema is unknown. But the condition runs in families in 20% to 60% of cases, so you may inherit it. The condition occurs almost exclusively in women. […] You’re more likely to get lipedema if you: Being female. Have a family history of lipedema. Have a BMI higher than 35. […] Lipedema slowly worsens with time in many people. […] Early diagnosis and treatment may help you avoid complications. Exercising and using compression stockings can give you a better outcome. Liposuction can help you feel better.
  • #37 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    Lipoedema is a chronic disease in adipose tissue that almost exclusively affects women during periods of hormonal alterations. Its main symptoms include an abnormal accumulation of subcutaneous fat in the buttock, hips, and legs, which is associated with pain, swelling, and easy bruising. […] Overall, research on lipoedema is scarce. As such, this study examined the health, health-related quality of life (HRQOL), and sense of coherence (SOC) among women with lipoedema. […] However, previous studies have revealed that lipoedema may affect approximately 10% of the female population. […] Currently, no specific biomarkers for diagnosing lipoedema are available, with it being confirmed solely through the use of a thorough medical history-taking and a comprehensive physical examination that includes both inspection and palpation.
  • #38 Biomarker for lipedema, other lymphatic diseases discovered | News Center
    https://med.stanford.edu/news/all-news/2020/11/biomarker-for-lipedema-discovered.html
    Lipedema is part of a family of medical problems called fat disorders and is often confused with obesity, said Stanley Rockson, MD, professor of cardiovascular medicine and the Allan and Tia Neill Professor of Lymphatic Research and Medicine at the Stanford School of Medicine. It causes fatty tissue to collect in the lower portion of the body, primarily the hips, but can affect the arms as well. It is often triggered by hormonal changes in women, particularly after life events such as puberty or pregnancy, or during menopause, but it also has a potential genetic component. Until recently, little was known about its scientific underpinnings. […] Now, for the first time, Rockson and his colleagues have uncovered a biomarker – in this case, a particular molecule that can be detected in patients – that confirms that lipedema is related to other lymphatic diseases, such as lymphedema, distinguishing it from obesity.
  • #39 European Journal of Translational and Clinical Medicine
    https://ejtcm.gumed.edu.pl/articles/201944
    Lipoedema is a chronic disease with various manifestation of symptoms, related to excessive deposition of subcutaneous adipose tissue in the legs, hips and buttocks. The scale of the problem is enormous and may affect up to one in five women. Lipoedema is often underdiagnosed and misdiagnosed with lymphedema, obesity or lipohypertrophy. In recent years, lipedema has been diagnosed in an increasing number of younger women, and its first symptoms may manifest already in puberty. […] Various studies have shown that lipoedema affects 11-19% of females. The estimated frequency of lipoedema in the general population varies between 0.06% and 19% depending on the study. However, typical symptoms of lipoedema are common among young women. First symptoms appear already in puberty or childhood (57.1-64.2% of cases). Also, a study of 209 patients with lipoedema showed that symptoms typically appear around age 16. In another, 70% of women with lipoedema experienced onset before age 30, but unfortunately only 1.6% were diagnosed earlier by a healthcare professional.
  • #40
    https://link.springer.com/article/10.1007/s13555-018-0241-6
    Lipoedema is a chronic disorder in which excessive fat distribution occurs predominantly from the waist down, resulting in a disproportion between the lower extremities and upper torso. […] To gain better understanding of this frequently neglected and misdiagnosed disorder, it is particular important to collect further epidemiological, clinical and therapeutic evidence. […] The onset of lipoedema is usually at or soon after puberty up to the third decade of life, with some cases reporting late onset after pregnancy or even menopause. […] Although lipoedema is not currently recognized as a hereditary disease, the familial nature of the condition suggests that lipoedema can demonstrate heritability. […] Lipoedema has a massive effect on patients lives, and approximately 85 % say lipoedema affects their mental health and ability to cope with life.
  • #41 Lipedema – USZ
    https://www.usz.ch/en/disease/lipedema/
    Lipoedema usually begins during a phase of hormonal changes such as puberty, pregnancy or the menopause. The frequency of lipoedema is not exactly known. This is probably because lipedema is very often confused with obesity or lymphedema. […] The first step is basic diagnostics, which consists of a detailed medical history and physical examination. […] For monitoring purposes, it is recommended to document further parameters such as weight, body mass index (BMI), waist-to-hip ratio (WHR), waist-to-height ratio (WTR) as well as circumference and volume measurements of the extremities and the daily activity index. […] Correct and early diagnosis and treatment of lipoedema improves the course of the disease. This means that the development of water retention can be slowed down and the symptoms alleviated. In addition, the risk of complications is reduced and the quality of life is improved.
  • #42 European Journal of Translational and Clinical Medicine
    https://ejtcm.gumed.edu.pl/articles/201944
    Lipoedema is a chronic disease with various manifestation of symptoms, related to excessive deposition of subcutaneous adipose tissue in the legs, hips and buttocks. The scale of the problem is enormous and may affect up to one in five women. Lipoedema is often underdiagnosed and misdiagnosed with lymphedema, obesity or lipohypertrophy. In recent years, lipedema has been diagnosed in an increasing number of younger women, and its first symptoms may manifest already in puberty. […] Various studies have shown that lipoedema affects 11-19% of females. The estimated frequency of lipoedema in the general population varies between 0.06% and 19% depending on the study. However, typical symptoms of lipoedema are common among young women. First symptoms appear already in puberty or childhood (57.1-64.2% of cases). Also, a study of 209 patients with lipoedema showed that symptoms typically appear around age 16. In another, 70% of women with lipoedema experienced onset before age 30, but unfortunately only 1.6% were diagnosed earlier by a healthcare professional.
  • #43 Lipedema: Causes, Symptoms & Treatment
    https://my.clevelandclinic.org/health/diseases/17175-lipedema
    Lipedema causes abnormal fat buildup in your lower body, getting worse over time. […] Researchers estimate that 1 in 72,000 people have lipedema. But this number is probably low because lipedema can look like obesity or lymphedema. Another global estimate says 11% of females have lipedema. The condition is rare in males. […] The exact cause of lipedema is unknown. But the condition runs in families in 20% to 60% of cases, so you may inherit it. The condition occurs almost exclusively in women. […] You’re more likely to get lipedema if you: Being female. Have a family history of lipedema. Have a BMI higher than 35. […] Lipedema slowly worsens with time in many people. […] Early diagnosis and treatment may help you avoid complications. Exercising and using compression stockings can give you a better outcome. Liposuction can help you feel better.
  • #44 Lipedema: Causes, Symptoms & Treatment
    https://my.clevelandclinic.org/health/diseases/17175-lipedema
    Lipedema causes abnormal fat buildup in your lower body, getting worse over time. […] Researchers estimate that 1 in 72,000 people have lipedema. But this number is probably low because lipedema can look like obesity or lymphedema. Another global estimate says 11% of females have lipedema. The condition is rare in males. […] The exact cause of lipedema is unknown. But the condition runs in families in 20% to 60% of cases, so you may inherit it. The condition occurs almost exclusively in women. […] You’re more likely to get lipedema if you: Being female. Have a family history of lipedema. Have a BMI higher than 35. […] Lipedema slowly worsens with time in many people. […] Early diagnosis and treatment may help you avoid complications. Exercising and using compression stockings can give you a better outcome. Liposuction can help you feel better.
  • #45 Investigation of clinical characteristics and genome associations in the ‘UK Lipoedema’ cohort | medRxiv
    https://www.medrxiv.org/content/10.1101/2021.06.15.21258988v1.full-text
    To investigate this hypothesis, we have conducted a Genome Wide Association Study (GWAS) to investigate genetic associations with the lipoedema trait. […] The cohort of patients were selected on strict clinical criteria. […] Identifying the possible genetic causes could help to better define lipoedema, facilitate the development of a diagnostic test, and could lead to possible treatments. […] The association analysis in the discovery cohort revealed multiple suggestive genomic loci associated with lipoedema. […] Approximately half the recruited women reported a family history of large legs, and this is consistent with the estimated SNP-based heritability of 50-60% calculated in the discovery cohort, indicating a strong genetic link to lipoedema. […] Despite a small cohort size, we believe the careful phenotyping has led to the identification of some putative regions of genetic association.
  • #46 Investigation of clinical characteristics and genome associations in the ‘UK Lipoedema’ cohort | medRxiv
    https://www.medrxiv.org/content/10.1101/2021.06.15.21258988v1.full-text
    To investigate this hypothesis, we have conducted a Genome Wide Association Study (GWAS) to investigate genetic associations with the lipoedema trait. […] The cohort of patients were selected on strict clinical criteria. […] Identifying the possible genetic causes could help to better define lipoedema, facilitate the development of a diagnostic test, and could lead to possible treatments. […] The association analysis in the discovery cohort revealed multiple suggestive genomic loci associated with lipoedema. […] Approximately half the recruited women reported a family history of large legs, and this is consistent with the estimated SNP-based heritability of 50-60% calculated in the discovery cohort, indicating a strong genetic link to lipoedema. […] Despite a small cohort size, we believe the careful phenotyping has led to the identification of some putative regions of genetic association.
  • #47 Investigation of clinical characteristics and genome associations in the ‘UK Lipoedema’ cohort | medRxiv
    https://www.medrxiv.org/content/10.1101/2021.06.15.21258988v1.full-text
    The top three SNPs in our analysis, rs1409440, rs7994616 and rs11616618, were located on chromosome 13 in a block of linkage disequilibrium (LD) close to the LHFPL6 gene. […] The GWAS participants from our cohort carrying the SNPs associated with LHFPL6 were significantly more likely to report direct maternal family history compared to the non-carriers. […] The meta-analysis of the discovery and replication cohorts also revealed six other distinct genetic loci putatively associated with the disease.
  • #48 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #49 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    Lipedema, a malady that is not well-understood, can detrimentally affect ones quality of life, ability to work, and healthcare costs. […] Despite the far-reaching effects of Lipedema and its potentially high rate of occurrence, there is still very little information about how many populations it affects, how often it interferes with peoples lives, and the accurate price of its healthcare. […] The lack of information on Lipedema is due to the lack of epidemiological studies. […] Accurate prevalence figures for Lipedema are essential to best address the issue. Without precise data, efforts to combat this condition are severely hindered. […] The majority of estimates highlight that Lipedema is not a rare condition. […] The exact Lipedema prevalence is uncertain, though a 2020 literature review suggests that 10-11% of women, or approximately 400 million people, have it.
  • #50 Diagnosis and management of lipedema – UpToDate
    https://www.uptodate.com/contents/diagnosis-and-management-of-lipedema
    Lipedema is defined by an International Consensus as „a chronic condition characterized by a disproportionate increase in adipose tissue and pain in the lower extremities, and sometimes, the upper extremities of females.” […] The true incidence of lipedema is unknown. Patients with lipedema were historically erroneously diagnosed with lymphedema and referred to lymphedema programs. Two studies reported that 4 percent of individuals referred with primary „lymphedema” actually had lipedema. […] Lipedema is a chronic condition with symmetric deposition of subcutaneous adipose tissue disproportionately in primarily the lower extremities. […] Because of the association with pain, International Consensus Guidelines have recommended renaming the disorder „lipalgia syndrome.”
  • #51 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    Lipoedema is a chronic disease in adipose tissue that almost exclusively affects women during periods of hormonal alterations. Its main symptoms include an abnormal accumulation of subcutaneous fat in the buttock, hips, and legs, which is associated with pain, swelling, and easy bruising. […] Overall, research on lipoedema is scarce. As such, this study examined the health, health-related quality of life (HRQOL), and sense of coherence (SOC) among women with lipoedema. […] However, previous studies have revealed that lipoedema may affect approximately 10% of the female population. […] Currently, no specific biomarkers for diagnosing lipoedema are available, with it being confirmed solely through the use of a thorough medical history-taking and a comprehensive physical examination that includes both inspection and palpation.
  • #52 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    Lipoedema is a chronic disease in adipose tissue that almost exclusively affects women during periods of hormonal alterations. Its main symptoms include an abnormal accumulation of subcutaneous fat in the buttock, hips, and legs, which is associated with pain, swelling, and easy bruising. […] Overall, research on lipoedema is scarce. As such, this study examined the health, health-related quality of life (HRQOL), and sense of coherence (SOC) among women with lipoedema. […] However, previous studies have revealed that lipoedema may affect approximately 10% of the female population. […] Currently, no specific biomarkers for diagnosing lipoedema are available, with it being confirmed solely through the use of a thorough medical history-taking and a comprehensive physical examination that includes both inspection and palpation.
  • #53 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    Lipoedema is a chronic disease in adipose tissue that almost exclusively affects women during periods of hormonal alterations. Its main symptoms include an abnormal accumulation of subcutaneous fat in the buttock, hips, and legs, which is associated with pain, swelling, and easy bruising. […] Overall, research on lipoedema is scarce. As such, this study examined the health, health-related quality of life (HRQOL), and sense of coherence (SOC) among women with lipoedema. […] However, previous studies have revealed that lipoedema may affect approximately 10% of the female population. […] Currently, no specific biomarkers for diagnosing lipoedema are available, with it being confirmed solely through the use of a thorough medical history-taking and a comprehensive physical examination that includes both inspection and palpation.
  • #54 Lipedema – Wikipedia
    https://en.wikipedia.org/wiki/Lipedema
    According to an epidemiologic study by Fldi E and Fldi M, lipedema affects 11% of the female population, although rates from 6-39% have also been reported. […] Lipedema is often underdiagnosed due to the difficulty in differentiating it from lymphedema, obesity, or other edemas.
  • #55 Differential diagnoses and treatment of lipedema
    https://www.oaepublish.com/articles/2347-9264.2019.51
    Lipedema is possibly a common but underdiagnosed disorder, which is almost exclusively found in females, but, as there is no standardized diagnostic test, the exact prevalence is unknown. According to German studies, 8%-18% of patients referred to a lymphedema clinic suffer from lipedema. […] The diagnosis of lipedema is usually based on medical history and clinical features. One criterion is the onset of the disease in parallel with hormonal changes and occurrence mainly in women. […] Lipedema is frequently misdiagnosed as obesity. While obesity affects the whole body, lipedema usually affects the upper and/or lower limbs and does not involve the feet and hands. […] A recent review highlights the utility of developing a genetic diagnostic test containing candidate genes for lipedema and causative genes of diseases that can be confused with lipedema, to help differentiate lipedema from other diagnoses.
  • #56 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    The leading symptom of lipoedema is pain. Other common symptoms include numbness, easy bruising, fatigue, muscle weakness, and feeling generally swollen. […] A study focusing on the psychological status and quality of life of people with lipoedema found that those with higher symptom severity reported lower levels of HRQOL. […] Women with lipoedema often describe experiences of unhelpful and misguided advice from healthcare professionals, resulting in them struggling to, by themselves, gather information in order to understand and manage their health problems. […] This study found that comorbidities among the participants were common. […] The fact that lipoedema is associated with diverse and multiple comorbidities has also been presented in previous studies. […] This study found that women with lipoedema reported a significantly lower HRQOL than does the general female population.
  • #57 Lipedema: Current Diagnostic and Treatment Evidence
    https://www.medscape.com/viewarticle/lipedema-current-diagnostic-and-treatment-evidence-2024a1000e0p
    During his presentation at the ICO, he shared studies on the efficacy of imaging exams such as ultrasound, tomography, and MRI in diagnosing the characteristic lipedema-associated increase in subcutaneous tissue. […] Despite the various diagnostic options, Murad highlighted two highly effective studies. […] A Brazilian study used ultrasound to establish a cutoff point of 11.7 mm in the pretibial subcutaneous tissue thickness, achieving 96% specificity for diagnosis. […] Another study emphasized the value of dual-energy x-ray absorptiometry (DXA), which demonstrated 95% sensitivity. […] Treatments for lipedema are still evolving, with considerable debate about the best approach. […] While some specialists advocate exclusively for conservative treatment, others recommend combining these methods with surgical interventions, depending on the stage of the disease.
  • #58 Lipedema: Current Diagnostic and Treatment Evidence
    https://www.medscape.com/viewarticle/lipedema-current-diagnostic-and-treatment-evidence-2024a1000e0p
    During his presentation at the ICO, he shared studies on the efficacy of imaging exams such as ultrasound, tomography, and MRI in diagnosing the characteristic lipedema-associated increase in subcutaneous tissue. […] Despite the various diagnostic options, Murad highlighted two highly effective studies. […] A Brazilian study used ultrasound to establish a cutoff point of 11.7 mm in the pretibial subcutaneous tissue thickness, achieving 96% specificity for diagnosis. […] Another study emphasized the value of dual-energy x-ray absorptiometry (DXA), which demonstrated 95% sensitivity. […] Treatments for lipedema are still evolving, with considerable debate about the best approach. […] While some specialists advocate exclusively for conservative treatment, others recommend combining these methods with surgical interventions, depending on the stage of the disease.
  • #59 Lipedema: Current Diagnostic and Treatment Evidence
    https://www.medscape.com/viewarticle/lipedema-current-diagnostic-and-treatment-evidence-2024a1000e0p
    During his presentation at the ICO, he shared studies on the efficacy of imaging exams such as ultrasound, tomography, and MRI in diagnosing the characteristic lipedema-associated increase in subcutaneous tissue. […] Despite the various diagnostic options, Murad highlighted two highly effective studies. […] A Brazilian study used ultrasound to establish a cutoff point of 11.7 mm in the pretibial subcutaneous tissue thickness, achieving 96% specificity for diagnosis. […] Another study emphasized the value of dual-energy x-ray absorptiometry (DXA), which demonstrated 95% sensitivity. […] Treatments for lipedema are still evolving, with considerable debate about the best approach. […] While some specialists advocate exclusively for conservative treatment, others recommend combining these methods with surgical interventions, depending on the stage of the disease.
  • #60 Biomarker for lipedema, other lymphatic diseases discovered | News Center
    https://med.stanford.edu/news/all-news/2020/11/biomarker-for-lipedema-discovered.html
    Lipedema is often confused with obesity because that’s what it looks like, and few doctors are trained to know the difference, Rockson said. […] „Many of these patients struggle with simple validation that they have a pathological entity,” said Rockson, who has been treating patients with the disorder and studying the lymphatic system for almost three decades. „This is a disease – it’s not their fault – yet they are often denied medical care and denied insurance coverage.” […] „We wanted to see if we could find a biological marker for lymphedema and lipedema, and discriminate between those and obesity,” Rockson said. […] „What we found when we did the protein analyses was that Pf4 was uniquely elevated in all three categories of patients with lymphatic disease,” Rockson said. „It very clearly established that lipedema has the same biomarker.”
  • #61 Lipedema: A Disease Triggered by M2 Polarized Macrophages?
    https://www.mdpi.com/2227-9059/13/3/561
    Lipedema studies are limited, and an inadequate number of participants further complicate therapeutically meaningful interpretations. It is well known that sample size is critical in clinical research, and experimental outcomes and conclusions, in terms of p-values, are less reliable when based on small cohorts. Thus, larger multicenter trials are recommended for the future. Lipedema is a common condition affecting mainly women during hormonal changes and represents a complex, yet poorly understood dysfunction involving macrophages, adipocytes, and endothelial cells. Impaired lymphatic endothelial function and increased permeability of lymph and blood vessels are early signs of dysfunction and disease onset. The identification of diagnostic markers for lipedema remains a challenge, but platelet factor 4 in plasma-derived exosomes is elevated in lipedema and has high sensitivity and specificity to discriminate patients with lipedema from controls. Other characteristic features in fat tissue of lipedema patients include the increased adipogenic potential of adipose tissue-derived stem cells, the higher number of stromal vascular cells, and the increased amount of M2 macrophages.
  • #62 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    Despite chronic pain and substantial limitations in daily activities and social life due to the associated health problems, many women live with lipoedema symptoms and uncertainty regarding their health for decades before being correctly diagnosed by a healthcare professional. […] The results from this study strongly indicate a failure in early detection, which then suggests that many women are forced to cope with health problems with either no or deficient support from healthcare services.
  • #63 Diagnosis – Lipoedema UK
    https://lipoedema.co.uk/about-lipoedema/diagnosis/
    A survey by Lipoedema UK (2021) highlighted that 57% of respondents experienced symptoms around puberty but only 2% received a diagnosis. A massive 62% of respondents stated they didn’t receive a diagnosis until later in life (between 41 and 80 years of age). […] It is important to obtain an early diagnosis of Lipoedema. This will start the process of finding the most effective way to manage symptoms. […] An early diagnosis of Lipoedema can help the person and their family, friends and colleagues understand the condition and why the changes in their body are happening, plus what can be done to help manage symptoms. Receiving a diagnosis can empower individuals to make changes to their lifestyle, health and wellbeing, which in turn can help manage symptoms and concerns. […] It is important to obtain an early diagnosis in order to be able to discuss treatment options that can help you to better manage symptoms and conditions. […] Individuals with Lipoedema may be referred by their GP to a local Lymphoedema Clinic as there are no specialist Lipoedema clinics in the NHS.
  • #64 Diagnosis – Lipoedema UK
    https://lipoedema.co.uk/about-lipoedema/diagnosis/
    A survey by Lipoedema UK (2021) highlighted that 57% of respondents experienced symptoms around puberty but only 2% received a diagnosis. A massive 62% of respondents stated they didn’t receive a diagnosis until later in life (between 41 and 80 years of age). […] It is important to obtain an early diagnosis of Lipoedema. This will start the process of finding the most effective way to manage symptoms. […] An early diagnosis of Lipoedema can help the person and their family, friends and colleagues understand the condition and why the changes in their body are happening, plus what can be done to help manage symptoms. Receiving a diagnosis can empower individuals to make changes to their lifestyle, health and wellbeing, which in turn can help manage symptoms and concerns. […] It is important to obtain an early diagnosis in order to be able to discuss treatment options that can help you to better manage symptoms and conditions. […] Individuals with Lipoedema may be referred by their GP to a local Lymphoedema Clinic as there are no specialist Lipoedema clinics in the NHS.
  • #65 Diagnosis – Lipoedema UK
    https://lipoedema.co.uk/about-lipoedema/diagnosis/
    A survey by Lipoedema UK (2021) highlighted that 57% of respondents experienced symptoms around puberty but only 2% received a diagnosis. A massive 62% of respondents stated they didn’t receive a diagnosis until later in life (between 41 and 80 years of age). […] It is important to obtain an early diagnosis of Lipoedema. This will start the process of finding the most effective way to manage symptoms. […] An early diagnosis of Lipoedema can help the person and their family, friends and colleagues understand the condition and why the changes in their body are happening, plus what can be done to help manage symptoms. Receiving a diagnosis can empower individuals to make changes to their lifestyle, health and wellbeing, which in turn can help manage symptoms and concerns. […] It is important to obtain an early diagnosis in order to be able to discuss treatment options that can help you to better manage symptoms and conditions. […] Individuals with Lipoedema may be referred by their GP to a local Lymphoedema Clinic as there are no specialist Lipoedema clinics in the NHS.
  • #66 Treating lipedema with liposuction may help women with 'painful fat’ disease | Wolters Kluwer
    https://www.wolterskluwer.com/en/news/treating-lipedema-with-liposuction-may-help-women-with-painful-fat-disease
    Lipedema is a congenital disease, causing disproportionate accumulations of fat, most often in the legs. […] Occurring almost exclusively in women, lipedema is usually misdiagnosed as obesity but the abnormal fat deposits don’t respond to diet or exercise. […] The average time to diagnosis was 15 years. […] The authors note some important limitations of their patient survey study. However, it adds to a growing body of evidence supporting the benefits of liposuction in reducing symptoms and improving quality of life for women with lipedema. […] Dr. Bauer and colleagues emphasize the need for further, in-depth studies to gain a clearer picture of the physiological mechanisms underlying this progressive disease.
  • #67 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    Despite chronic pain and substantial limitations in daily activities and social life due to the associated health problems, many women live with lipoedema symptoms and uncertainty regarding their health for decades before being correctly diagnosed by a healthcare professional. […] The results from this study strongly indicate a failure in early detection, which then suggests that many women are forced to cope with health problems with either no or deficient support from healthcare services.
  • #68 Lipedema – USZ
    https://www.usz.ch/en/disease/lipedema/
    Lipoedema usually begins during a phase of hormonal changes such as puberty, pregnancy or the menopause. The frequency of lipoedema is not exactly known. This is probably because lipedema is very often confused with obesity or lymphedema. […] The first step is basic diagnostics, which consists of a detailed medical history and physical examination. […] For monitoring purposes, it is recommended to document further parameters such as weight, body mass index (BMI), waist-to-hip ratio (WHR), waist-to-height ratio (WTR) as well as circumference and volume measurements of the extremities and the daily activity index. […] Correct and early diagnosis and treatment of lipoedema improves the course of the disease. This means that the development of water retention can be slowed down and the symptoms alleviated. In addition, the risk of complications is reduced and the quality of life is improved.
  • #69 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #70 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    However, the studies used in this review are based mainly on European populations, which could skew the overall picture. […] A British dermatology department documented 67 Lipedema cases over 15 years, yielding a minimum prevalence of 0.001%. […] An online screening tool in Brazil showed that 12.3% of respondents met the Lipedema criteria, while a Germany screening found that 4.8-9.7% had moderate to severe Lipedema. […] This means Lipedema is relatively common in women. […] While Lipedema occurs almost exclusively in women, Lipedemas precise prevalence is uncertain. […] This knowledge gap is mainly due to inadequate studies of epidemiology. […] The economic effects of Lipedema are not well known due to a lack of prevalence data. […] To understand the financial burden Lipedema patients face in terms of healthcare and employment, a more precise picture of the associated costs must be established. […] Obtaining accurate information on the frequency of Lipedema continues to be a difficult endeavor due to the significant financial and temporal expenditure required for conducting quality epidemiological research.
  • #71 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #72 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    A Brazil-based online screening tool indicated that 12.3% of respondents would meet criteria for Lipedema, whereas one screening in Germany found 4.8-9.7% of participants had moderate to pronounced Lipedema. […] In addition to identifying Lipedemas prevalence, we also need to better understand the prevalence of specific symptoms in the disease. […] Without robust data from systematic, large-scale surveys, the true prevalence of these symptoms remains unclear, and it is difficult to identify the most urgently needed treatments. […] Although Lipedema may be mistaken for other health conditions, people with Lipedema may also have other conditions. […] If we knew how often these comorbidities overlap with Lipedema, clinicians could build better care plans and researchers could better quantify the diseases economic toll.
  • #73 Lipedema, lymphedema, lipohypertrophy, and obesity: how do we differentiate? – Servier – PhlebolymphologyServier – Phlebolymphology
    https://www.phlebolymphology.org/lipedema-lymphedema-lipohypertrophy-and-obesity-how-do-we-differentiate/
    Lymphological and fatty tissue disorders of the legs are increasingly tying up capacities in the health care system. […] Over 50 years, this condition has been underdiagnosed. […] Many studies are still needed to better understand the entity lipedema, and efforts are underway to change the name to avoid misunderstandings, as the condition lipedema does not seem to have water in the fatty tissue. […] Even though first described in the 1950s, it wasn’t until 2000 that interest was focused on knowledge of the condition lipedema. […] The differential diagnosis is even made more difficult by incorrect information spread through social media, suggesting that disproportion (ie, lipohypertrophy) equals lipedema, that lipedema inevitably causes psychological harm to the affected women, and that increase in body weight is unavoidably associated with lipedema.
  • #74 Lipedema’s invisible toll – Harvard Health
    https://www.health.harvard.edu/diseases-and-conditions/lipedemas-invisible-toll
    Lipedema has been reported to affect as many as 12% of women around the world, but the true incidence is unknown. […] Many women with the condition are misdiagnosed. […] Lipedema is more common than people would guess. […] We really don’t have a sense of how common, but we know it’s underdiagnosed. […] Because of the dearth of research and the fact that many doctors don’t understand the condition some patients go years before receiving an accurate diagnosis. […] Lack of awareness about lipedema is perhaps the greatest impediment to receiving an accurate diagnosis.
  • #75 What is Lipedema: Causes, Symptoms, and Treatment | Lipedema Canada
    https://lipedemacanada.org/what-is-lipedema/
    Estimates suggest that up to 11% of females worldwide may have the condition. […] The absence of diagnostic tools, medical and public unawareness of the disease, and the weight gain stigma contribute to the unknown number of people suffering from lipedema and its epidemiology. […] Navigating Lipedema can be especially challenging in Canada due to the lack of awareness of the condition among healthcare providers.
  • #76 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    Lipedema, a poorly understood disease characterized by irregular fat distribution and accumulation, can dramatically impact quality of life, workforce participation, and healthcare costs. […] Yet despite Lipedemas impacts and a high estimated prevalence of the disease, we know little about how frequently it manifests in different populations, how regularly symptoms disrupt daily life, or its precise healthcare costs. […] Accurate and innovative prevalence data is necessary to understand the true dimensions and impacts of Lipedema. […] A literature review published in 2020 estimated that 10-11% of womensome 400 million peoplehave Lipedema. […] One British dermatology department documented 67 Lipedema cases in 15 years, resulting in a minimum prevalence estimate of 0.001% although the authors noted this is likely an underestimate.
  • #77 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    Lipedema, a malady that is not well-understood, can detrimentally affect ones quality of life, ability to work, and healthcare costs. […] Despite the far-reaching effects of Lipedema and its potentially high rate of occurrence, there is still very little information about how many populations it affects, how often it interferes with peoples lives, and the accurate price of its healthcare. […] The lack of information on Lipedema is due to the lack of epidemiological studies. […] Accurate prevalence figures for Lipedema are essential to best address the issue. Without precise data, efforts to combat this condition are severely hindered. […] The majority of estimates highlight that Lipedema is not a rare condition. […] The exact Lipedema prevalence is uncertain, though a 2020 literature review suggests that 10-11% of women, or approximately 400 million people, have it.
  • #78 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #79 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    However, the studies used in this review are based mainly on European populations, which could skew the overall picture. […] A British dermatology department documented 67 Lipedema cases over 15 years, yielding a minimum prevalence of 0.001%. […] An online screening tool in Brazil showed that 12.3% of respondents met the Lipedema criteria, while a Germany screening found that 4.8-9.7% had moderate to severe Lipedema. […] This means Lipedema is relatively common in women. […] While Lipedema occurs almost exclusively in women, Lipedemas precise prevalence is uncertain. […] This knowledge gap is mainly due to inadequate studies of epidemiology. […] The economic effects of Lipedema are not well known due to a lack of prevalence data. […] To understand the financial burden Lipedema patients face in terms of healthcare and employment, a more precise picture of the associated costs must be established. […] Obtaining accurate information on the frequency of Lipedema continues to be a difficult endeavor due to the significant financial and temporal expenditure required for conducting quality epidemiological research.
  • #80 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    The leading symptom of lipoedema is pain. Other common symptoms include numbness, easy bruising, fatigue, muscle weakness, and feeling generally swollen. […] A study focusing on the psychological status and quality of life of people with lipoedema found that those with higher symptom severity reported lower levels of HRQOL. […] Women with lipoedema often describe experiences of unhelpful and misguided advice from healthcare professionals, resulting in them struggling to, by themselves, gather information in order to understand and manage their health problems. […] This study found that comorbidities among the participants were common. […] The fact that lipoedema is associated with diverse and multiple comorbidities has also been presented in previous studies. […] This study found that women with lipoedema reported a significantly lower HRQOL than does the general female population.
  • #81 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    The leading symptom of lipoedema is pain. Other common symptoms include numbness, easy bruising, fatigue, muscle weakness, and feeling generally swollen. […] A study focusing on the psychological status and quality of life of people with lipoedema found that those with higher symptom severity reported lower levels of HRQOL. […] Women with lipoedema often describe experiences of unhelpful and misguided advice from healthcare professionals, resulting in them struggling to, by themselves, gather information in order to understand and manage their health problems. […] This study found that comorbidities among the participants were common. […] The fact that lipoedema is associated with diverse and multiple comorbidities has also been presented in previous studies. […] This study found that women with lipoedema reported a significantly lower HRQOL than does the general female population.
  • #82 Lipedema: A Relatively Common Disease with Extremely Common Misconceptions
    https://pmc.ncbi.nlm.nih.gov/articles/PMC5055019/
    Lipedema, or adiposis dolorosa, is a common adipose tissue disorder that is believed to affect nearly 11% of adult women worldwide. […] With an incidence that may affect nearly 1 in 9 adult women, it is important to generate appropriate awareness, conduct additional research, and identify better diagnostic and treatment modalities for lipedema so these women can obtain the care that they need and deserve. […] If estimates are correct, lipedema may affect millions of women in the United States alone, with an estimated incidence of 1 in 9 adult women. […] Despite its description in 1940 by Allen and Hines, little is understood about the adipose tissue disorder, lipedema. […] One of the greatest difficulties with treatment of lipedema is insurance coverage for the surgical treatment. […] With an incidence that may affect nearly 1 in 9 adult women, it is important to generate appropriate awareness, conduct additional research, and identify better diagnostic and treatment modalities so these women can obtain the care that they need and deserve.
  • #83
    https://journals.lww.com/prsgo/fulltext/2016/09000/lipedema__a_relatively_common_disease_with.12.aspx
    The diagnostic criteria for lipedema were first described in 1951 by Wold et al and have been modified in recent years by Herbst. […] Lipedema almost exclusively occurs in women, with the onset typically by the third decade of life. […] Because of its relatively unknown status in the medical community, there is a paucity of conclusive, supportive data regarding effective treatments of this disease. […] One of the greatest difficulties with treatment of lipedema is insurance coverage for the surgical treatment. […] With an incidence that may affect nearly 1 in 9 adult women, it is important to generate appropriate awareness, conduct additional research, and identify better diagnostic and treatment modalities so these women can obtain the care that they need and deserve.
  • #84 Observational Study on a Large Italian Population with Lipedema: Biochemical and Hormonal Profile, Anatomical and Clinical Evaluation, Self-Reported History
    https://www.mdpi.com/1422-0067/25/3/1599
    We analyzed the medical condition of 360 women affected by lipedema of the lower limbs in stages 1, 2, and 3. […] The true prevalence of lipedema is unknown, although it is thought to be a common disease. The estimated prevalence ranges from 6.5% in children in the United States and 6–8% in women in Germany to 15–19% in vascular disease clinics. […] The diagnosis of lipedema is clinical and is carried out through the evaluation of diagnostic criteria helpful in framing the characteristics of the pathological tissue. […] The standard conservative therapy for lipedema includes specific physiotherapy and nutritional treatments, compression garments, and specific motor physical activity plans. […] This study aimed to analyze the medical history and the clinical, ultrasound, and laboratory characteristics of a large number of Italian women affected by lipedema. No previous study has reported data on Italian women affected by lipedema.
  • #85 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #86 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    However, the studies used in this review are based mainly on European populations, which could skew the overall picture. […] A British dermatology department documented 67 Lipedema cases over 15 years, yielding a minimum prevalence of 0.001%. […] An online screening tool in Brazil showed that 12.3% of respondents met the Lipedema criteria, while a Germany screening found that 4.8-9.7% had moderate to severe Lipedema. […] This means Lipedema is relatively common in women. […] While Lipedema occurs almost exclusively in women, Lipedemas precise prevalence is uncertain. […] This knowledge gap is mainly due to inadequate studies of epidemiology. […] The economic effects of Lipedema are not well known due to a lack of prevalence data. […] To understand the financial burden Lipedema patients face in terms of healthcare and employment, a more precise picture of the associated costs must be established. […] Obtaining accurate information on the frequency of Lipedema continues to be a difficult endeavor due to the significant financial and temporal expenditure required for conducting quality epidemiological research.
  • #87 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    The leading symptom of lipoedema is pain. Other common symptoms include numbness, easy bruising, fatigue, muscle weakness, and feeling generally swollen. […] A study focusing on the psychological status and quality of life of people with lipoedema found that those with higher symptom severity reported lower levels of HRQOL. […] Women with lipoedema often describe experiences of unhelpful and misguided advice from healthcare professionals, resulting in them struggling to, by themselves, gather information in order to understand and manage their health problems. […] This study found that comorbidities among the participants were common. […] The fact that lipoedema is associated with diverse and multiple comorbidities has also been presented in previous studies. […] This study found that women with lipoedema reported a significantly lower HRQOL than does the general female population.
  • #88
    https://link.springer.com/article/10.1007/s13555-018-0241-6
    Lipoedema is a chronic disorder in which excessive fat distribution occurs predominantly from the waist down, resulting in a disproportion between the lower extremities and upper torso. […] To gain better understanding of this frequently neglected and misdiagnosed disorder, it is particular important to collect further epidemiological, clinical and therapeutic evidence. […] The onset of lipoedema is usually at or soon after puberty up to the third decade of life, with some cases reporting late onset after pregnancy or even menopause. […] Although lipoedema is not currently recognized as a hereditary disease, the familial nature of the condition suggests that lipoedema can demonstrate heritability. […] Lipoedema has a massive effect on patients lives, and approximately 85 % say lipoedema affects their mental health and ability to cope with life.
  • #89 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    The leading symptom of lipoedema is pain. Other common symptoms include numbness, easy bruising, fatigue, muscle weakness, and feeling generally swollen. […] A study focusing on the psychological status and quality of life of people with lipoedema found that those with higher symptom severity reported lower levels of HRQOL. […] Women with lipoedema often describe experiences of unhelpful and misguided advice from healthcare professionals, resulting in them struggling to, by themselves, gather information in order to understand and manage their health problems. […] This study found that comorbidities among the participants were common. […] The fact that lipoedema is associated with diverse and multiple comorbidities has also been presented in previous studies. […] This study found that women with lipoedema reported a significantly lower HRQOL than does the general female population.
  • #90 Lipoedema – is a paradigm shift needed? | CarEdOn
    https://www.caredon.org/blog/lipoedema-paradigm-shift-needed
    Lipoedema is a chronic condition in women characterized by a disproportionate increase in adipose tissue in the legs (sometimes in the arms) together with pain (or/and tender to touch the skin) in this adipose tissue. […] Research on lipoedema is scarce, and clear diagnostic tools are lacking. This contributes to the fact that the prevalence rate of lipoedema is largely unknown. In a recently published US lipoedema guideline, it was stated that prevalence estimates range from 6.5% in children in the US, 6%-8% in women in Germany, and 15%-19% in vascular clinics. […] Consequently, purely lipoedema does not include oedema, neither is there any scientific evidence for lymphatic insufficiency. Therefore, decongestive lymphatic treatment is inappropriate for patients with purely lipoedema. […] Up to now, a chronic low-grade state of inflammation and tissue hypoxia are the most plausible explanations for the pain experienced in lipoedema patients.
  • #91 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    The leading symptom of lipoedema is pain. Other common symptoms include numbness, easy bruising, fatigue, muscle weakness, and feeling generally swollen. […] A study focusing on the psychological status and quality of life of people with lipoedema found that those with higher symptom severity reported lower levels of HRQOL. […] Women with lipoedema often describe experiences of unhelpful and misguided advice from healthcare professionals, resulting in them struggling to, by themselves, gather information in order to understand and manage their health problems. […] This study found that comorbidities among the participants were common. […] The fact that lipoedema is associated with diverse and multiple comorbidities has also been presented in previous studies. […] This study found that women with lipoedema reported a significantly lower HRQOL than does the general female population.
  • #92
    https://link.springer.com/article/10.1007/s13555-018-0241-6
    Lipoedema is a chronic disorder in which excessive fat distribution occurs predominantly from the waist down, resulting in a disproportion between the lower extremities and upper torso. […] To gain better understanding of this frequently neglected and misdiagnosed disorder, it is particular important to collect further epidemiological, clinical and therapeutic evidence. […] The onset of lipoedema is usually at or soon after puberty up to the third decade of life, with some cases reporting late onset after pregnancy or even menopause. […] Although lipoedema is not currently recognized as a hereditary disease, the familial nature of the condition suggests that lipoedema can demonstrate heritability. […] Lipoedema has a massive effect on patients lives, and approximately 85 % say lipoedema affects their mental health and ability to cope with life.
  • #93 Biomarker for lipedema, other lymphatic diseases discovered | News Center
    https://med.stanford.edu/news/all-news/2020/11/biomarker-for-lipedema-discovered.html
    The discovery of this biomarker also now creates potential for a blood test to diagnose lymphatic diseases in outpatient settings, Rockson said. Current methods of diagnosing both lymphedema and lipedema involve invasive and expensive imaging procedures and aren’t often used. A simple blood test could be a game changer, he said. […] „Lipedema patients feel totally abandoned, and rightfully so,” Rockson said. „They have a disease that turns life upside-down and are told there is nothing wrong with them. To dignify it with proper identification is very important to people.” […] „We know the degree and level of bias against fat,” she said. „I’ve heard it thousands of times from women like me. 'My doctor says I’m fat, that I need to lose weight, that it’s my fault.’ If there’s pain, it’s ascribed to emotional or psychological issues. To confirm that it’s actually a disease is a breakthrough.”
  • #94 Women’s health: Lipoedema patients forgotten by NHS
    https://www.bbc.com/news/videos/cevxjypdn7mo
    A woman diagnosed with a painful fat condition called lipoedema said she feels lonely because of a lack of support and understanding that she is not obese. […] Lipoedema causes fat to abnormally build-up mainly in the hips, buttocks and legs, leading to a disproportionate shape. […] The exact cause of the chronic condition is unknown but it is not from being overweight. It may be caused by changes in hormones, and is believed to affect about 11% of people worldwide. […] The 45-year-old said there was no support from the NHS for patients with her condition other than compression.
  • #95 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    Lipedema, a poorly understood disease characterized by irregular fat distribution and accumulation, can dramatically impact quality of life, workforce participation, and healthcare costs. […] Yet despite Lipedemas impacts and a high estimated prevalence of the disease, we know little about how frequently it manifests in different populations, how regularly symptoms disrupt daily life, or its precise healthcare costs. […] Accurate and innovative prevalence data is necessary to understand the true dimensions and impacts of Lipedema. […] A literature review published in 2020 estimated that 10-11% of womensome 400 million peoplehave Lipedema. […] One British dermatology department documented 67 Lipedema cases in 15 years, resulting in a minimum prevalence estimate of 0.001% although the authors noted this is likely an underestimate.
  • #96 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    The leading symptom of lipoedema is pain. Other common symptoms include numbness, easy bruising, fatigue, muscle weakness, and feeling generally swollen. […] A study focusing on the psychological status and quality of life of people with lipoedema found that those with higher symptom severity reported lower levels of HRQOL. […] Women with lipoedema often describe experiences of unhelpful and misguided advice from healthcare professionals, resulting in them struggling to, by themselves, gather information in order to understand and manage their health problems. […] This study found that comorbidities among the participants were common. […] The fact that lipoedema is associated with diverse and multiple comorbidities has also been presented in previous studies. […] This study found that women with lipoedema reported a significantly lower HRQOL than does the general female population.
  • #97 Diagnosis – Lipoedema UK
    https://lipoedema.co.uk/about-lipoedema/diagnosis/
    A survey by Lipoedema UK (2021) highlighted that 57% of respondents experienced symptoms around puberty but only 2% received a diagnosis. A massive 62% of respondents stated they didn’t receive a diagnosis until later in life (between 41 and 80 years of age). […] It is important to obtain an early diagnosis of Lipoedema. This will start the process of finding the most effective way to manage symptoms. […] An early diagnosis of Lipoedema can help the person and their family, friends and colleagues understand the condition and why the changes in their body are happening, plus what can be done to help manage symptoms. Receiving a diagnosis can empower individuals to make changes to their lifestyle, health and wellbeing, which in turn can help manage symptoms and concerns. […] It is important to obtain an early diagnosis in order to be able to discuss treatment options that can help you to better manage symptoms and conditions. […] Individuals with Lipoedema may be referred by their GP to a local Lymphoedema Clinic as there are no specialist Lipoedema clinics in the NHS.
  • #98 Lipedema – USZ
    https://www.usz.ch/en/disease/lipedema/
    Lipoedema usually begins during a phase of hormonal changes such as puberty, pregnancy or the menopause. The frequency of lipoedema is not exactly known. This is probably because lipedema is very often confused with obesity or lymphedema. […] The first step is basic diagnostics, which consists of a detailed medical history and physical examination. […] For monitoring purposes, it is recommended to document further parameters such as weight, body mass index (BMI), waist-to-hip ratio (WHR), waist-to-height ratio (WTR) as well as circumference and volume measurements of the extremities and the daily activity index. […] Correct and early diagnosis and treatment of lipoedema improves the course of the disease. This means that the development of water retention can be slowed down and the symptoms alleviated. In addition, the risk of complications is reduced and the quality of life is improved.
  • #99 Lipedema – USZ
    https://www.usz.ch/en/disease/lipedema/
    Lipoedema usually begins during a phase of hormonal changes such as puberty, pregnancy or the menopause. The frequency of lipoedema is not exactly known. This is probably because lipedema is very often confused with obesity or lymphedema. […] The first step is basic diagnostics, which consists of a detailed medical history and physical examination. […] For monitoring purposes, it is recommended to document further parameters such as weight, body mass index (BMI), waist-to-hip ratio (WHR), waist-to-height ratio (WTR) as well as circumference and volume measurements of the extremities and the daily activity index. […] Correct and early diagnosis and treatment of lipoedema improves the course of the disease. This means that the development of water retention can be slowed down and the symptoms alleviated. In addition, the risk of complications is reduced and the quality of life is improved.
  • #100 Lipedema – USZ
    https://www.usz.ch/en/disease/lipedema/
    Lipoedema usually begins during a phase of hormonal changes such as puberty, pregnancy or the menopause. The frequency of lipoedema is not exactly known. This is probably because lipedema is very often confused with obesity or lymphedema. […] The first step is basic diagnostics, which consists of a detailed medical history and physical examination. […] For monitoring purposes, it is recommended to document further parameters such as weight, body mass index (BMI), waist-to-hip ratio (WHR), waist-to-height ratio (WTR) as well as circumference and volume measurements of the extremities and the daily activity index. […] Correct and early diagnosis and treatment of lipoedema improves the course of the disease. This means that the development of water retention can be slowed down and the symptoms alleviated. In addition, the risk of complications is reduced and the quality of life is improved.
  • #101 Diagnosis – Lipoedema UK
    https://lipoedema.co.uk/about-lipoedema/diagnosis/
    A survey by Lipoedema UK (2021) highlighted that 57% of respondents experienced symptoms around puberty but only 2% received a diagnosis. A massive 62% of respondents stated they didn’t receive a diagnosis until later in life (between 41 and 80 years of age). […] It is important to obtain an early diagnosis of Lipoedema. This will start the process of finding the most effective way to manage symptoms. […] An early diagnosis of Lipoedema can help the person and their family, friends and colleagues understand the condition and why the changes in their body are happening, plus what can be done to help manage symptoms. Receiving a diagnosis can empower individuals to make changes to their lifestyle, health and wellbeing, which in turn can help manage symptoms and concerns. […] It is important to obtain an early diagnosis in order to be able to discuss treatment options that can help you to better manage symptoms and conditions. […] Individuals with Lipoedema may be referred by their GP to a local Lymphoedema Clinic as there are no specialist Lipoedema clinics in the NHS.
  • #102 Diagnosis – Lipoedema UK
    https://lipoedema.co.uk/about-lipoedema/diagnosis/
    A survey by Lipoedema UK (2021) highlighted that 57% of respondents experienced symptoms around puberty but only 2% received a diagnosis. A massive 62% of respondents stated they didn’t receive a diagnosis until later in life (between 41 and 80 years of age). […] It is important to obtain an early diagnosis of Lipoedema. This will start the process of finding the most effective way to manage symptoms. […] An early diagnosis of Lipoedema can help the person and their family, friends and colleagues understand the condition and why the changes in their body are happening, plus what can be done to help manage symptoms. Receiving a diagnosis can empower individuals to make changes to their lifestyle, health and wellbeing, which in turn can help manage symptoms and concerns. […] It is important to obtain an early diagnosis in order to be able to discuss treatment options that can help you to better manage symptoms and conditions. […] Individuals with Lipoedema may be referred by their GP to a local Lymphoedema Clinic as there are no specialist Lipoedema clinics in the NHS.
  • #103 Diagnosis – Lipoedema UK
    https://lipoedema.co.uk/about-lipoedema/diagnosis/
    A survey by Lipoedema UK (2021) highlighted that 57% of respondents experienced symptoms around puberty but only 2% received a diagnosis. A massive 62% of respondents stated they didn’t receive a diagnosis until later in life (between 41 and 80 years of age). […] It is important to obtain an early diagnosis of Lipoedema. This will start the process of finding the most effective way to manage symptoms. […] An early diagnosis of Lipoedema can help the person and their family, friends and colleagues understand the condition and why the changes in their body are happening, plus what can be done to help manage symptoms. Receiving a diagnosis can empower individuals to make changes to their lifestyle, health and wellbeing, which in turn can help manage symptoms and concerns. […] It is important to obtain an early diagnosis in order to be able to discuss treatment options that can help you to better manage symptoms and conditions. […] Individuals with Lipoedema may be referred by their GP to a local Lymphoedema Clinic as there are no specialist Lipoedema clinics in the NHS.
  • #104 Women with lipoedema: a national survey on their health, health-related quality of life, and sense of coherence | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-022-02022-3
    Despite chronic pain and substantial limitations in daily activities and social life due to the associated health problems, many women live with lipoedema symptoms and uncertainty regarding their health for decades before being correctly diagnosed by a healthcare professional. […] The results from this study strongly indicate a failure in early detection, which then suggests that many women are forced to cope with health problems with either no or deficient support from healthcare services.
  • #105 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #106 Lipedema: a clinical entity | Łyszczak | Acta Angiologica
    https://journals.viamedica.pl/acta_angiologica/article/view/60081
    Lipedema is a chronic, progressive disorder of adipose tissue, found almost exclusively in women, that involves disproportionate subcutaneous fat depositions, leading to progressive and symmetric enlargement of the legs. […] There is an urgent need for further studies on the pathogenesis of lipedema, epidemiology, diagnostic criteria and possible curative treatment. […] Lymphatic disturbances in lipoedema.
  • #107 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #108 Thieme E-Journals – Archives of Plastic Surgery / Abstract
    https://www.thieme-connect.com/products/ejournals/abstract/10.1055/a-2530-5875
    Lipedema is an adipose tissue disorder that principally affects women and is frequently misidentified as obesity or lymphedema. […] There have been relatively few studies that have precisely defined the pathogenesis, epidemiology, and treatment approaches for lipedema. […] This review aimed to examine the existing literature on the epidemiology, pathogenesis, clinical presentation, differential diagnosis, and treatments for lipedema. […] The current research indicates that lipedema appears to be a clinical entity related to genetic factors and fat distribution, although distinct from lymphedema and obesity. […] Further high-quality randomized controlled trials are urgently needed to continue advancing our understanding of this often neglected disease and exploring optimal medical and surgical treatment regimens tailored specifically for lipedema patients.
  • #109 Investigation of clinical characteristics and genome associations in the ‘UK Lipoedema’ cohort | medRxiv
    https://www.medrxiv.org/content/10.1101/2021.06.15.21258988v1.full-text
    To investigate this hypothesis, we have conducted a Genome Wide Association Study (GWAS) to investigate genetic associations with the lipoedema trait. […] The cohort of patients were selected on strict clinical criteria. […] Identifying the possible genetic causes could help to better define lipoedema, facilitate the development of a diagnostic test, and could lead to possible treatments. […] The association analysis in the discovery cohort revealed multiple suggestive genomic loci associated with lipoedema. […] Approximately half the recruited women reported a family history of large legs, and this is consistent with the estimated SNP-based heritability of 50-60% calculated in the discovery cohort, indicating a strong genetic link to lipoedema. […] Despite a small cohort size, we believe the careful phenotyping has led to the identification of some putative regions of genetic association.
  • #110 European Journal of Translational and Clinical Medicine
    https://ejtcm.gumed.edu.pl/articles/201944
    The available data is insufficient to reveal the specific prevalence of lipoedema in the general population. Lack of accurate diagnostic markers of lipoedema and confusion regarding its definition results in a high rate of misdiagnosis and wrong mistreatment, which may imply rare diagnosis. […] Diagnosis is usually made in middle-aged women, although first symptoms can manifest in puberty, which suggest a hormonal basis of lipoedema. […] It is crucial to define the pathophysiology of lipoedema and find accurate, easily-available diagnostic markers. Clinical trials could help establish causal treatment. We need a holistic approach (with psychological support) to patients with lipoedema, standardization of patient care, improved differential diagnosis and awareness, not only among patients, but also in the training of future healthcare professionals.
  • #111 Key signaling networks are dysregulated in patients with the adipose tissue disorder, lipedema | International Journal of Obesity
    https://www.nature.com/articles/s41366-021-01002-1
    Lipedema, a poorly understood chronic disease of adipose hyper-deposition, is often mistaken for obesity and causes significant impairment to mobility and quality-of-life. […] Despite a relatively high incidence of lipedema, molecular or genetic data to explain the pathogenesis of the disease are lacking. […] Our findings substantially improve understanding of the molecular mechanisms underpinning lipedema and will be useful for identifying disease biomarkers and targets for future therapeutics with which to combat this devastating disease. […] Our integrated approach uncovered deranged metabolic and lipid profiles, and dysregulated signaling pathways driving key biological processes, such as adipogenesis, cell cycle, lipid metabolism, and cell proliferation and differentiation. […] Importantly, the findings of our multimodal study were coherent across distinct biological platforms and provide new insights that will both help to address the deficit in lipoedema animal models and provide vital clues into potential novel therapeutic approaches.
  • #112 Key signaling networks are dysregulated in patients with the adipose tissue disorder, lipedema | International Journal of Obesity
    https://www.nature.com/articles/s41366-021-01002-1
    The gene expression profiles defined in lipedema whole tissue and ADSCs highlighted potential molecular drivers of lipedema. […] Our data indicate that Bub1 overexpression promotes ADSC hyperproliferation in lipedema and may therefore play a key role in lipedema disease onset and progression. […] The findings of this study present, for the first time, a useful platform for pinpointing diagnostic biomarkers that may be predictive of lipedema disease progression.
  • #113 Investigation of clinical characteristics and genome associations in the ‘UK Lipoedema’ cohort | medRxiv
    https://www.medrxiv.org/content/10.1101/2021.06.15.21258988v1.full-text
    Lipoedema is a chronic adipose tissue disorder mainly affecting women, causing excess subcutaneous fat deposition on the lower limbs with pain and tenderness. […] A tightly phenotyped cohort of 200 lipoedema patients was recruited from two UK specialist clinics. […] The analysis revealed genetic loci suggestively associated with the lipoedema phenotype, with further support provided by an independent cohort taken from the 100,000 Genomes Project. […] This first GWAS of a UK lipoedema cohort has identified genetic regions of suggestive association with the disease. […] The diagnosis of lipoedema can be difficult to make if lymphoedema and/or obesity co-exist. […] One of the major problems with the diagnosis of lipoedema is the lack of a confirmatory test. […] Family history has been reported in lipoedema patients suggesting a familial origin of the disease but many cases also appear to be sporadic.
  • #114 Differential diagnoses and treatment of lipedema
    https://www.oaepublish.com/articles/2347-9264.2019.51
    Lipedema is possibly a common but underdiagnosed disorder, which is almost exclusively found in females, but, as there is no standardized diagnostic test, the exact prevalence is unknown. According to German studies, 8%-18% of patients referred to a lymphedema clinic suffer from lipedema. […] The diagnosis of lipedema is usually based on medical history and clinical features. One criterion is the onset of the disease in parallel with hormonal changes and occurrence mainly in women. […] Lipedema is frequently misdiagnosed as obesity. While obesity affects the whole body, lipedema usually affects the upper and/or lower limbs and does not involve the feet and hands. […] A recent review highlights the utility of developing a genetic diagnostic test containing candidate genes for lipedema and causative genes of diseases that can be confused with lipedema, to help differentiate lipedema from other diagnoses.
  • #115
    https://www.dw.com/en/lipedema-has-nothing-to-do-with-obesity-or-a-poor-diet/a-64286432
    Epidemiological studies do not yet exist, meaning it is difficult to know exactly how many women are affected. Estimates put it at around 370 million worldwide. Experts think there are differences in how lipedema manifests around the world. […] In Germany, probably one in ten women suffers from it. In general, Caucasian women in Europe are particularly affected. In Asia, on the other hand, lipedema is not known at all. There is a special form in African women they tend to develop lipedema in the hip area and above the rump. There it occurs more frequently in the form of painful so-called breech fat.
  • #116 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #117 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://lipedema.net/how-prevalent-is-lipedema-in-women/
    While Lipedema occurs almost exclusively in women, Lipedemas precise prevalence is uncertain. This knowledge gap is mainly due to inadequate studies of epidemiology. […] Obtaining accurate information on the frequency of Lipedema continues to be a difficult endeavor due to the significant financial and temporal expenditure required for conducting quality epidemiological research. […] The economic effects of Lipedema are not well known due to a lack of prevalence data. To understand the financial burden Lipedema patients face in terms of healthcare and employment, a more precise picture of the associated costs must be established. […] The difficult nature of epidemiology research notwithstanding, it may hold the key to transforming the way Lipedema is explored and treated. Through more accurate estimates of its prevalence, we can illustrate to those in charge of funding and policy-making the significance of investigations into Lipedema and increase encouragement for future studies that are creative and advanced.
  • #118 Session 9 – Epidemiology and Diagnostic Tools (Video) – LIPEDEMA WORLD CONGRESS 2023
    https://www.lipedema-world-congress.com/on-demand/session-9-epidemiology-and-diagnostic-tools-video/
    Lipedema -epidemiological data with reference to the current care situation in Germany based on a collective of 8.7 million insured people […] A comparison study of potential translational screening tools for lipedema.
  • #119 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    A Brazil-based online screening tool indicated that 12.3% of respondents would meet criteria for Lipedema, whereas one screening in Germany found 4.8-9.7% of participants had moderate to pronounced Lipedema. […] In addition to identifying Lipedemas prevalence, we also need to better understand the prevalence of specific symptoms in the disease. […] Without robust data from systematic, large-scale surveys, the true prevalence of these symptoms remains unclear, and it is difficult to identify the most urgently needed treatments. […] Although Lipedema may be mistaken for other health conditions, people with Lipedema may also have other conditions. […] If we knew how often these comorbidities overlap with Lipedema, clinicians could build better care plans and researchers could better quantify the diseases economic toll.
  • #120 Assessment of lipoedema awareness among polish women- online survey study | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-023-02614-7
    Lipoedema is an adipose tissue disorder that is still not fully understood. The primary purpose of this study is to explore the state of knowledge and understanding of lipoedema among Polish women. The secondary aim is to investigate the possible association between knowledge and factors such as BMI, self-reported symptoms, and age. […] Awareness of lipoedema among women is deficient. A significant proportion of the respondents report the occurrence of lipoedema symptoms. In order to improve the situation of lipoedema patients, it is crucial to increase the knowledge about this condition both among medical professionals and the general public. […] The major problem that women with lipoedema face is a large number of misdiagnosed cases. The low awareness both among medical professionals and the general public leads to an incorrect diagnosis, the condition is usually diagnosed as obesity or lymphoedema.
  • #121 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #122 About Lipedema — Lipedema Foundation
    https://www.lipedema.org/about-lipedema
    Lipedema is a chronic condition that occurs almost exclusively in women and manifests as symmetrical buildup of often-painful fat in the limbs, sparing the hands and feet. […] As a result, the true number of women with Lipedema, or its epidemiology, is unknown. […] In 2023, the Lipedema Foundation published the Research Roadmap. The Roadmap identifies recommendations to strengthen and expand Lipedema research, enhance knowledge, reduce barriers, facilitate exchange of ideas, and advance best practices.
  • #123 9. Renaming the term ‘lipoedema’ – Issuu
    https://issuu.com/canadianlymphedemaframework/docs/jwc_consensus_lipoedema/s/25619746
    As already suggested decades ago, it is necessary to change the term lipoedema. […] A multi-centre study using high-resolution ultrasound focusing on patients diagnosed with lipoedema failed to identify any indication of fluid in the soft tissue in the legs. […] In a seminal article published in 2012, Reich-Schupke et al called the term lipoedema misleading, stating that it is not an oedema or a fluid retention in the tissue. […] The European Lipedema Forum, a high-ranking international group of experts from seven European countries, then concluded in a noteworthy consensus paper that there is no scientific evidence that lipoedema is an oedema problem. […] The previously lipoedema/liposuction task force has issued a statement on the fact that lipoedema does not include oedema. […] The changes in perspectives on lipoedema described here bring the patients real symptoms to the forefront, allowing for more comprehensive and sustainable treatment.
  • #124 Lipoedema – is a paradigm shift needed? | CarEdOn
    https://www.caredon.org/blog/lipoedema-paradigm-shift-needed
    Therefore, therapeutic approaches to lipoedema should focus on these causes of pain. […] Based the aforementioned arguments, the authors of the consensus guideline plead for a change of the term lipoedema. […] It is hoped that the new suggested term lipalgia syndrome will quickly become internationally recognized and gain widespread usage.
  • #125 9. Renaming the term ‘lipoedema’ – Issuu
    https://issuu.com/canadianlymphedemaframework/docs/jwc_consensus_lipoedema/s/25619746
    As already suggested decades ago, it is necessary to change the term lipoedema. […] A multi-centre study using high-resolution ultrasound focusing on patients diagnosed with lipoedema failed to identify any indication of fluid in the soft tissue in the legs. […] In a seminal article published in 2012, Reich-Schupke et al called the term lipoedema misleading, stating that it is not an oedema or a fluid retention in the tissue. […] The European Lipedema Forum, a high-ranking international group of experts from seven European countries, then concluded in a noteworthy consensus paper that there is no scientific evidence that lipoedema is an oedema problem. […] The previously lipoedema/liposuction task force has issued a statement on the fact that lipoedema does not include oedema. […] The changes in perspectives on lipoedema described here bring the patients real symptoms to the forefront, allowing for more comprehensive and sustainable treatment.
  • #126 Diagnosis and management of lipedema – UpToDate
    https://www.uptodate.com/contents/diagnosis-and-management-of-lipedema
    Lipedema is defined by an International Consensus as „a chronic condition characterized by a disproportionate increase in adipose tissue and pain in the lower extremities, and sometimes, the upper extremities of females.” […] The true incidence of lipedema is unknown. Patients with lipedema were historically erroneously diagnosed with lymphedema and referred to lymphedema programs. Two studies reported that 4 percent of individuals referred with primary „lymphedema” actually had lipedema. […] Lipedema is a chronic condition with symmetric deposition of subcutaneous adipose tissue disproportionately in primarily the lower extremities. […] Because of the association with pain, International Consensus Guidelines have recommended renaming the disorder „lipalgia syndrome.”
  • #127 Lipoedema – is a paradigm shift needed? | CarEdOn
    https://www.caredon.org/blog/lipoedema-paradigm-shift-needed
    Therefore, therapeutic approaches to lipoedema should focus on these causes of pain. […] Based the aforementioned arguments, the authors of the consensus guideline plead for a change of the term lipoedema. […] It is hoped that the new suggested term lipalgia syndrome will quickly become internationally recognized and gain widespread usage.
  • #128 Lipoedema – is a paradigm shift needed? | CarEdOn
    https://www.caredon.org/blog/lipoedema-paradigm-shift-needed
    Lipoedema is a chronic condition in women characterized by a disproportionate increase in adipose tissue in the legs (sometimes in the arms) together with pain (or/and tender to touch the skin) in this adipose tissue. […] Research on lipoedema is scarce, and clear diagnostic tools are lacking. This contributes to the fact that the prevalence rate of lipoedema is largely unknown. In a recently published US lipoedema guideline, it was stated that prevalence estimates range from 6.5% in children in the US, 6%-8% in women in Germany, and 15%-19% in vascular clinics. […] Consequently, purely lipoedema does not include oedema, neither is there any scientific evidence for lymphatic insufficiency. Therefore, decongestive lymphatic treatment is inappropriate for patients with purely lipoedema. […] Up to now, a chronic low-grade state of inflammation and tissue hypoxia are the most plausible explanations for the pain experienced in lipoedema patients.
  • #129 9. Renaming the term ‘lipoedema’ – Issuu
    https://issuu.com/canadianlymphedemaframework/docs/jwc_consensus_lipoedema/s/25619746
    As already suggested decades ago, it is necessary to change the term lipoedema. […] A multi-centre study using high-resolution ultrasound focusing on patients diagnosed with lipoedema failed to identify any indication of fluid in the soft tissue in the legs. […] In a seminal article published in 2012, Reich-Schupke et al called the term lipoedema misleading, stating that it is not an oedema or a fluid retention in the tissue. […] The European Lipedema Forum, a high-ranking international group of experts from seven European countries, then concluded in a noteworthy consensus paper that there is no scientific evidence that lipoedema is an oedema problem. […] The previously lipoedema/liposuction task force has issued a statement on the fact that lipoedema does not include oedema. […] The changes in perspectives on lipoedema described here bring the patients real symptoms to the forefront, allowing for more comprehensive and sustainable treatment.
  • #130 Lipedema, lymphedema, lipohypertrophy, and obesity: how do we differentiate? – Servier – PhlebolymphologyServier – Phlebolymphology
    https://www.phlebolymphology.org/lipedema-lymphedema-lipohypertrophy-and-obesity-how-do-we-differentiate/
    A lot of work is needed to address this misleading information with 2 goals. […] The diagnosis of these 4 entities is based on medical history, visual inspection, and palpation. […] An improvement of the definitions of these entities including the renaming of lipedema disease to avoid conception of edema associated with lipedema is needed.
  • #131 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #132 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    Lipedema, a malady that is not well-understood, can detrimentally affect ones quality of life, ability to work, and healthcare costs. […] Despite the far-reaching effects of Lipedema and its potentially high rate of occurrence, there is still very little information about how many populations it affects, how often it interferes with peoples lives, and the accurate price of its healthcare. […] The lack of information on Lipedema is due to the lack of epidemiological studies. […] Accurate prevalence figures for Lipedema are essential to best address the issue. Without precise data, efforts to combat this condition are severely hindered. […] The majority of estimates highlight that Lipedema is not a rare condition. […] The exact Lipedema prevalence is uncertain, though a 2020 literature review suggests that 10-11% of women, or approximately 400 million people, have it.
  • #133 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #134 Lipedema, lymphedema, lipohypertrophy, and obesity: how do we differentiate? – Servier – PhlebolymphologyServier – Phlebolymphology
    https://www.phlebolymphology.org/lipedema-lymphedema-lipohypertrophy-and-obesity-how-do-we-differentiate/
    Lymphological and fatty tissue disorders of the legs are increasingly tying up capacities in the health care system. […] Over 50 years, this condition has been underdiagnosed. […] Many studies are still needed to better understand the entity lipedema, and efforts are underway to change the name to avoid misunderstandings, as the condition lipedema does not seem to have water in the fatty tissue. […] Even though first described in the 1950s, it wasn’t until 2000 that interest was focused on knowledge of the condition lipedema. […] The differential diagnosis is even made more difficult by incorrect information spread through social media, suggesting that disproportion (ie, lipohypertrophy) equals lipedema, that lipedema inevitably causes psychological harm to the affected women, and that increase in body weight is unavoidably associated with lipedema.
  • #135 Assessment of lipoedema awareness among polish women- online survey study | BMC Women’s Health | Full Text
    https://bmcwomenshealth.biomedcentral.com/articles/10.1186/s12905-023-02614-7
    According to the present knowledge, lipoedema is a chronic disease and it cannot be fully cured through a conservative approach. […] The exact prevalence remains unknown however various data provide estimated values varying from 7 to 19% of the female population. […] Overall knowledge of lipoedema in our study was low as the correct definition of lipoedema was indicated by 7% of women, and 4%, 12%, and 37% could mark the correct methods of treatment, clinical features, and durability of lipoedema respectively. […] Our research may help spread knowledge about lipoedema both among medical professionals and the general population, which could have an impact on decreasing the number of undiagnosed cases.
  • #136 Lipedema: A Population Health Perspective – Recognizing the Signs and Empowering Women with Holistic Health Assessment  | CMSA
    https://cmsa.org/lipedema-a-population-health-perspective-recognizing-the-signs-and-empowering-women-with-holistic-health-assessment/
    Lipedema, a chronic tissue disorder, affects about 10%–11% of women, or approximately 400 million worldwide. Yet, it remains a largely misunderstood condition. […] Early recognition of lipedema can significantly improve health outcomes and quality of life. […] To tackle Lipedema, healthcare must: educate providers for better diagnosis, increase public awareness, implement routine screenings, secure more research funding, advocate for insurance coverage of treatments. […] To ensure all women receive the care they deserve, we must reduce delays in diagnosis, expand access to specialized care, and address potential underdiagnosis.
  • #137 Demystifying Lipoedema: the urgent need for understanding this little-known and stigmatised disease | On.Praxhub
    https://on.praxhub.com/understanding-lipoedema
    Lipoedema is a disease of the loose connective tissues leading to dysregulated and abnormal growth of mainly fatty tissue. This results in disfiguring and painful adipose tissue that appears disproportionate to the size and shape of the affected persons body. It affects 11% of women worldwide and is very commonly misdiagnosed as lymphoedema or obesity. […] An urgent need for increased awareness and understanding among clinicians exists so that patients can be correctly diagnosed and evidence-based treatments options offered, and so that harmful narratives about this phenotype can be eliminated. […] Outline the epidemiology of lipoedema and its impacts on affected patients.
  • #138 Lipedema: A Population Health Perspective – Recognizing the Signs and Empowering Women with Holistic Health Assessment  | CMSA
    https://cmsa.org/lipedema-a-population-health-perspective-recognizing-the-signs-and-empowering-women-with-holistic-health-assessment/
    Lipedema, a chronic tissue disorder, affects about 10%–11% of women, or approximately 400 million worldwide. Yet, it remains a largely misunderstood condition. […] Early recognition of lipedema can significantly improve health outcomes and quality of life. […] To tackle Lipedema, healthcare must: educate providers for better diagnosis, increase public awareness, implement routine screenings, secure more research funding, advocate for insurance coverage of treatments. […] To ensure all women receive the care they deserve, we must reduce delays in diagnosis, expand access to specialized care, and address potential underdiagnosis.
  • #139 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #140 Lipedema: a clinical entity | Łyszczak | Acta Angiologica
    https://journals.viamedica.pl/acta_angiologica/article/view/60081
    Lipedema is a chronic, progressive disorder of adipose tissue, found almost exclusively in women, that involves disproportionate subcutaneous fat depositions, leading to progressive and symmetric enlargement of the legs. […] There is an urgent need for further studies on the pathogenesis of lipedema, epidemiology, diagnostic criteria and possible curative treatment. […] Lymphatic disturbances in lipoedema.
  • #141 Lipedema: A Relatively Common Disease with Extremely Common Misconceptions
    https://pmc.ncbi.nlm.nih.gov/articles/PMC5055019/
    Lipedema, or adiposis dolorosa, is a common adipose tissue disorder that is believed to affect nearly 11% of adult women worldwide. […] With an incidence that may affect nearly 1 in 9 adult women, it is important to generate appropriate awareness, conduct additional research, and identify better diagnostic and treatment modalities for lipedema so these women can obtain the care that they need and deserve. […] If estimates are correct, lipedema may affect millions of women in the United States alone, with an estimated incidence of 1 in 9 adult women. […] Despite its description in 1940 by Allen and Hines, little is understood about the adipose tissue disorder, lipedema. […] One of the greatest difficulties with treatment of lipedema is insurance coverage for the surgical treatment. […] With an incidence that may affect nearly 1 in 9 adult women, it is important to generate appropriate awareness, conduct additional research, and identify better diagnostic and treatment modalities so these women can obtain the care that they need and deserve.
  • #142 SciELO Brazil – Prevalência e fatores de risco para lipedema no Brasil Prevalência e fatores de risco para lipedema no Brasil
    https://www.scielo.br/j/jvb/a/Q9yR3XdzXVbrsB37KQD3mfg/?lang=en
    Lipedema is characterized as an abnormal deposition of fat in the buttocks and legs bilaterally that may be accompanied by swelling, pain, and tenderness. The estimated prevalence in Europe varies between 0.06% and 39%. […] The estimated prevalence of lipedema in the population of Brazilian women is 12.3%. […] The literature reports estimated prevalence rates of lipedema in the German population ranging from 0.06% to 39%. […] The most widely-accepted lipedema prevalence reported in the literature was estimated by Fldi and Fldi, who extrapolated their clinical experience to the general population, estimating that up to 11% of the female population may have lipedema. […] According to Schwahn-Schreiber and Marshall, the prevalence in Germany of all stages of lipedema is as great as 39% of the population. […] We estimate, conservatively, that 8.8 million adult Brazilian women aged 18 to 69 years may have symptoms suggestive of a diagnosis of lipedema.
  • #143 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #144 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://www.lipedema.net/how-prevalent-is-lipedema-in-women.html
    Lipedema, a malady that is not well-understood, can detrimentally affect ones quality of life, ability to work, and healthcare costs. […] Despite the far-reaching effects of Lipedema and its potentially high rate of occurrence, there is still very little information about how many populations it affects, how often it interferes with peoples lives, and the accurate price of its healthcare. […] The lack of information on Lipedema is due to the lack of epidemiological studies. […] Accurate prevalence figures for Lipedema are essential to best address the issue. Without precise data, efforts to combat this condition are severely hindered. […] The majority of estimates highlight that Lipedema is not a rare condition. […] The exact Lipedema prevalence is uncertain, though a 2020 literature review suggests that 10-11% of women, or approximately 400 million people, have it.
  • #145 Lipedema: a clinical entity | Łyszczak | Acta Angiologica
    https://journals.viamedica.pl/acta_angiologica/article/view/60081
    Lipedema is a chronic, progressive disorder of adipose tissue, found almost exclusively in women, that involves disproportionate subcutaneous fat depositions, leading to progressive and symmetric enlargement of the legs. […] There is an urgent need for further studies on the pathogenesis of lipedema, epidemiology, diagnostic criteria and possible curative treatment. […] Lymphatic disturbances in lipoedema.
  • #146 Thieme E-Journals – Archives of Plastic Surgery / Abstract
    https://www.thieme-connect.com/products/ejournals/abstract/10.1055/a-2530-5875
    Lipedema is an adipose tissue disorder that principally affects women and is frequently misidentified as obesity or lymphedema. […] There have been relatively few studies that have precisely defined the pathogenesis, epidemiology, and treatment approaches for lipedema. […] This review aimed to examine the existing literature on the epidemiology, pathogenesis, clinical presentation, differential diagnosis, and treatments for lipedema. […] The current research indicates that lipedema appears to be a clinical entity related to genetic factors and fat distribution, although distinct from lymphedema and obesity. […] Further high-quality randomized controlled trials are urgently needed to continue advancing our understanding of this often neglected disease and exploring optimal medical and surgical treatment regimens tailored specifically for lipedema patients.
  • #147 Lipedema Prevalence Research: Why Quality Data Matters — Lipedema Foundation
    https://www.lipedema.org/blog/2023/6/30/lipedema-prevalence-research-why-quality-data-matters
    The precise economic burden of Lipedema is largely hidden due to incomplete prevalence data. […] Despite the urgent need for accurate data on Lipedema prevalence, there are still substantial challenges to collecting this information. […] High-quality epidemiology studies require significant financial resources and time. […] Instead, we may need more innovative approaches to prevalence studies. […] This analysis demonstrates how, despite challenges, we can leverage innovative approaches and existing resources to further our knowledge of this disease’s prevalence and mechanisms. […] With more precise prevalence estimates, we can demonstrate to funders and policy makers the importance of Lipedema research and public health approaches and broaden support for a wide range of innovative future research.
  • #148 How Common is Lipedema in Women? – Lipedema Medical Solutions
    https://lipedema.net/how-prevalent-is-lipedema-in-women/
    While Lipedema occurs almost exclusively in women, Lipedemas precise prevalence is uncertain. This knowledge gap is mainly due to inadequate studies of epidemiology. […] Obtaining accurate information on the frequency of Lipedema continues to be a difficult endeavor due to the significant financial and temporal expenditure required for conducting quality epidemiological research. […] The economic effects of Lipedema are not well known due to a lack of prevalence data. To understand the financial burden Lipedema patients face in terms of healthcare and employment, a more precise picture of the associated costs must be established. […] The difficult nature of epidemiology research notwithstanding, it may hold the key to transforming the way Lipedema is explored and treated. Through more accurate estimates of its prevalence, we can illustrate to those in charge of funding and policy-making the significance of investigations into Lipedema and increase encouragement for future studies that are creative and advanced.