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Lipedema is a chronic, progressive disorder of adipose tissue that predominantly affects women, characterized by symmetrical fat accumulation in the extremities, pain, and resistance to caloric restriction. Recent insights suggest that lipedema represents a hormone-driven gynecological fat disorder, in which estrogen receptor (ER) imbalance plays a central role. The predominance of ERβ activity and suppression of ERα signaling are hypothesized to drive adipose hypertrophy, fibrosis, and inflammation, particularly in the context of intracrine estradiol excess. This model aligns lipedema with other estrogen-sensitive conditions, such as endometriosis and uterine fibroids, and provides a novel framework for understanding its pathophysiology. Therapeutically, this reframing opens new perspectives for hormonal modulation using selective progestins (drospirenone, gestrinone) and metabolic adjuncts such as tirzepatide, beyond the current symptomatic or surgical approaches.

Aim To explore the experiences of sexual health and intimate relationships in women with lipedema. Design A qualitative interview study. Methods Sixteen women with lipedema recruited from a national lipedema association group in Sweden participated. Data were collected between October 2023 and February 2024 and analysed using content analysis. Results Four main categories were identified. Being burdened by body shame highlighted the women's body dissatisfaction, difficulties in self-acceptance and shame when being naked in front of their partners. Being hindered by an aching and heavy body captured the experiences of bodily pain and heaviness in intimate situations. Being torn between desire and avoidance revealed that the women longed for intimacy but adopted different strategies to avoid it. Being affected by what is said and what is left unsaid showed the role of the partner's approach as well as the strain of not discussing sexual problems with partners or healthcare providers. Conclusion Women with lipedema experience physical, psychological and relational challenges in sexual life and intimacy. Still, these challenges remain unaddressed in healthcare settings. Implications for the Profession and Patient Care Nurses and midwives should, in their unique role in encountering women throughout their lifespans, address and invite dialogues on sexual-related concerns of women affected by lipedema. Impact The study findings provide insights into how lipedema affects women's sexual health and intimate relationships and offer new knowledge that can be applied when planning targeted interventions to promote the sexual health and well-being of women with lipedema. Reporting Method Adherence to the EQUATOR guidelines and COREQ checklist. Patient or Public Contribution Two patient representatives from a lipedema association group contributed to this study by distributing study information to their members.

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, lipoedema has been diagnosed in an increasing number of younger women, and its first symptoms may manifest already in puberty. Even though it is often perceived as only an aesthetic problem, it has a huge impact on the quality of life, mental health, self-esteem or self-confidence. Moreover, lipoedema causes stigmatization, unfortunately also in healthcare professionals. Nevertheless, recently, diagnostic criteria (also ultrasound) have been created, and lipoedema has been classified in ICD-10 (E88.2). There are also more and more treatment options, with emphasis on the role of psychological care. Awareness and knowledge of lipoedema have also increased despite its underestimation but still is not enough. The multidimensional nature of lipoedema and its impact on many aspects of life highlights the essential role of comprehensive support to patients. Nowadays, in times of caring for mental health, it is crucial to increase public awareness and spread knowledge about lipoedema.

Background: Lipedema is a chronic disorder characterized by symmetrical and disproportionate fat accumulation, pain, and easy bruising, often resistant to conventional treatments. Functional dysmetria (FD), a maladaptive neuromotor response linked to epigenetic stress, has been proposed as a relevant contributor to pain in lipedema., Objective: This retrospective observational study aimed to evaluate whether correcting FD through the radioelectric asymmetric conveyer (REAC) technology Neuropostural Optimization (NPO) protocol can reduce pain in patients with lipedema, using a sham-controlled design., Methods: In this retrospective observational study, 83 consecutive women with stage 2-5 lipedema underwent both sham and real NPO procedures during a single session. Pain intensity was measured using the visual analog scale (VAS) immediately after each procedure. Statistical analyses were performed using paired t-tests with effect sizes (Cohen’s dz) and 95% confidence intervals., Results: Baseline pain was uniformly high (mean 7.41 ± 0.53), with some pre-sham values reaching 10/10. Pain reduction was observed exclusively after real NPO and not after sham. Sham NPO induced no significant changes, whereas real NPO yielded a mean pain reduction exceeding 3.5 VAS points across all stages (mean change -3.65 ± 0.62; 95% CI: -3.79 to -3.51; Cohen’s dz = 5.88, 95% CI: 4.85-6.92; p < 0.0001)., Conclusions: These findings suggest that correction of FD by REAC NPO provides rapid and clinically meaningful analgesic effects in lipedema patients, addressing an upstream neuropsychomotor dysfunction that may contribute to disease progression. However, given the retrospective single-center design and absence of long-term follow-up, these conclusions are limited to the short-term effects observed. Further multicenter and longitudinal studies are warranted to confirm these results and evaluate long-term outcomes.

Objective: Lipedema, a chronic disorder of subcutaneous adipose tissue, is common yet often overlooked in clinical practice and frequently mistaken for obesity. Ultrasonographic (US) imaging methods beyond clinical examination have not been sufficiently studied in the differential diagnosis. The aim of this study is to investigate whether quantitative, AI‑assisted radiomics analysis of lower‑limb US images adds diagnostic value for lipedema. Methods: The study included ultrasonographic scans from four women with clinically confirmed lipedema and four age-matched women with obesity (BMI ≥ 30 kg/m²) referred to Dokuz Eylül University, Faculty of Medicine, Department of Physical Therapy and Rehabilitation outpatient clinic with suspected lipedema. All examinations were performed in the outpatient musculoskeletal US unit by an experienced radiologist. Using fixed depth, sector width and gain settings, eight images per leg were obtained at four standardised sites (2): mid‑anterior thigh, pretibial mid‑shaft, mid‑lateral leg, and medial supramalleolar region (Fig. 1). Also dermal and subcutaneous thicknesses were recorded. The optimal image area (region of interest = ROI) was labeled in these retrospective images, and radiomics analysis (tissue texture) was performed in the system. For this purpose, the LIFEx program (www.lifexsoft.org) was used. With this method, various pattern features were extracted from the determined ROIs. Dimensionality reduction techniques such as feature selection or Principal Component Analysis (PCA) were used to reduce the data size, which increased with the extracted features. The resulting dataset was analyzed for clinically significant results in images with lipedema. Given the small sample (n = 4 per group), group differences were evaluated with an independent‑samples t‑test using sample bootstrapping (100 resamples). Results: Radiomics features were compared between groups using a bootstrapped t-test. Within the intensity‑based category, Mean Intensity (p < 0.001) and Intensity Skewness (p = 0.01) differed significantly between lipedema and obesity images. From the grey‑level co‑occurrence matrix (GLCM), both Contrast (p < 0.001) and Dissimilarity (p = 0.02) showed significant difference. In addition, the grey‑level run‑length matrix (GLRLM) feature High Grey Level (p = 0.003) and the grey‑level size‑zone matrix (GLSZM) feature Grey Level Variance (p = 0.03) were statistically distinct between groups. No statistically significant differences were detected in dermal or subcutaneous thicknesses, except for dermis thickness at site A on the right limb, which reached significance (p = 0.04). Conclusion: This preliminary study suggests that quantitative ultrasonographic analysis enhanced by artificial intelligence–based radiomics may provide supportive diagnostic value in distinguishing lipedema from obesity. Larger-scale studies are needed to validate these preliminary findings. Keywords: Lipedema, Obesity, Radiomics Analysis, Artificial Intelligence

Purpose The aim of this study was to explore the functioning of people with lipoedema from their perspective. Methods This was a qualitative study following a phenomenological perspective using individual in-depth interviews with a convenience sample of 13 Dutch people with lipoedema. The data were analysed by using an interpretative phenomenological approach. Results Two overarching group experiential themes (GETs) were identified: (1) “physical complaints are only a part of their problems”, and (2) “longing for improved appearance and functioning”. The GETs were composed of the following subordinate GETs: “disproportionate functioning of the lower body”, “navigating daily life with lipoedema”, “coping with uncertainty”, “the toll of shame and stigmatization”, “consequences of a very negative self-image”, “desire for change and improved appearance and functioning”, and “an ongoing journey of acceptance”. Conclusions Participants experience that physical complaints affect daily activities, but with adequate adaptability, participation issues are relatively limited. Instead, shame about their appearance and (fear of) stigmatization mainly leads to social avoidance. Additionally, participants long for freedom to do what they want, wear what they want, and desire a different appearance. Therefore, the experienced level of acceptance of the condition is context- and situation-dependent and not straightforward, which is complicated by the burden of knowing that the condition is chronic.