# The Hidden Link Between Endometriosis and Obesity: A State-of-the-Art Review

**Authors:** Shefali N Desai, Christina C Reed, Yamely Mendez, Qiannan Yang, Xiaoming Guan

PMC · DOI: 10.7759/cureus.102896 · 2026-02-03

## TL;DR

This review explores the complex relationship between endometriosis and obesity, highlighting shared inflammatory pathways and challenges in diagnosis and treatment.

## Contribution

The paper synthesizes current knowledge on how obesity and endometriosis interact through adipokine signaling and treatment potential with glucagon-like peptide-1.

## Key findings

- Obesity and endometriosis share inflammatory markers like leptin and interleukin-6.
- Glucagon-like peptide-1 may reduce inflammation and macrophage infiltration in endometriosis.
- Obesity complicates endometriosis diagnosis due to poor visualization and surgical challenges.

## Abstract

Endometriosis remains an under-researched disease with a wide range of symptoms. Endometriosis reduces a woman's quality of life and professional productivity, yet its exact causes, risk factors, and treatment have yet to be elucidated. Body mass index and endometriosis have been observed to be inversely related; however, this relationship may only be a correlation rather than a causation. Obesity may play a role in the inflammation and cell proliferation associated with endometriosis through the complex signaling pathways of adipokines. A literature review was done on endometriosis and obesity to gain insight and synthesize knowledge about opportunities to improve endometriosis care, its inflammatory pathogenesis, and the treatment potential of glucagon-like peptide-1. A Boolean search was performed via the Texas Medical Center Library with keywords including "endometriosis", "adipose tissue", "obesity", "adipokines", "glucagon-like peptide-1", and "inflammation". After screening titles, abstracts, and full texts, articles were excluded due to irrelevance, lack of access to full-text, and repetition. The literature revealed that at the onset of endometriosis symptoms in obese women, chronic pelvic pain and decreased appetite could cause misdiagnosis and weight loss, lowering the incidence of endometriosis in the obese population. Poor visualization, ventilatory compromise, and conversion to laparotomy during laparoscopy hinders diagnostic quality for obese patients. Interestingly, endometriosis and obesity share similar pathological markers, including leptin, adiponectin, tumor-necrosis-factor-α, and interleukin-6. Finally, glucagon-like peptide-1 was found to decrease pro-inflammatory secretions and macrophage infiltration.

## Linked entities

- **Proteins:** lepa (leptin a), IL6 (interleukin 6)
- **Diseases:** endometriosis (MONDO:0005133), obesity (MONDO:0011122)

## Full-text entities

- **Genes:** POMC (proopiomelanocortin) [NCBI Gene 5443] {aka ACTH, CLIP, LPH, MSH, NPP, OBAIRH}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, FAT1 (FAT atypical cadherin 1) [NCBI Gene 2195] {aka CDHF7, CDHR8, FAT, ME5, hFat1}, NPY (neuropeptide Y) [NCBI Gene 4852] {aka PYY4}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, RARRES2 (retinoic acid receptor responder 2) [NCBI Gene 5919] {aka HP10433, TIG2}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, APLN (apelin) [NCBI Gene 8862] {aka APEL, XNPEP2}, LEPR (leptin receptor) [NCBI Gene 3953] {aka CD295, LEP-R, LEPRD, OB-R, OBR, huB219}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}, Gcg (glucagon) [NCBI Gene 14526] {aka GLP-1, Glu, PPG}, Lep (leptin) [NCBI Gene 16846] {aka ob, obese}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}, GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, RETN (resistin) [NCBI Gene 56729] {aka ADSF, FIZZ3, RENT, RETN1, RSTN, XCP1}, AGRP (agouti related neuropeptide) [NCBI Gene 181] {aka AGRT, ART, ASIP2}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** chronic pain (MESH:D059350), breast cancer (MESH:D001943), depression (MESH:D003866), musculoskeletal or gastrointestinal conditions (MESH:D009140), endometrial lesions (MESH:D014591), type 2 diabetes (MESH:D003924), systemic (MESH:D015619), type two diabetes (MESH:D003922), bowel perforation (MESH:D057112), infertility (MESH:D007246), musculoskeletal or gastrointestinal disorders (MESH:D005767), cardiovascular disease (MESH:D002318), insulin resistance (MESH:D007333), weight loss (MESH:D015431), wound infections (MESH:D014946), Pelvic Pain (MESH:D017699), dysmenorrhea (MESH:D004412), endometrial cancer (MESH:D016889), polycystic ovarian syndrome (MESH:D011085), I or II (MESH:D056829), fevers (MESH:D005334), Obesity (MESH:D009765), endometriotic lesions (MESH:D009059), hormone-sensitive cancers (MESH:D009369), blood loss (MESH:D016063), Edema (MESH:D004487), fibrosis (MESH:D005355), ovarian cysts (MESH:D010048), Inflammation (MESH:D007249), Endometriosis (MESH:D004715), dyslipidemia (MESH:D050171), brachial plexus injury (MESH:D020516), pain (MESH:D010146)
- **Chemicals:** glucose (MESH:D005947), steroid (MESH:D013256), glycogen (MESH:D006003), exenatide (MESH:D000077270)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12962185/full.md

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Source: https://tomesphere.com/paper/PMC12962185