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Endometriosis-associated infertility: Multi-omics insights into pathogenesis and precision therapeutics

子宫内膜异位症 发病机制 不育 组学 精密医学 生物信息学 医学 计算生物学 生物 遗传学 内科学 病理 怀孕
作者
Yuyi Ou,Hao Wang,Cankun Zhou,Yonglian Chen,Jun Lyu,Minqing Feng,Xiaobin Huang
出处
期刊:Frontiers in Endocrinology [Frontiers Media]
卷期号:16
标识
DOI:10.3389/fendo.2025.1613334
摘要

Introduction Endometriosis is a prevalent, estrogen-dependent, inflammatory disease that impairs fertility via hormonal dysregulation, immune dysfunction, oxidative stress/ferroptosis, genetic and epigenetic alterations, and microbiome imbalance. We summarize multi-omics insights and clinical implications for endometriosis-associated infertility. Methods This article is a Systematic Review that synthesizes recent multi-omics and clinical evidence on mechanisms (hormonal, immune-inflammatory, oxidative stress/ferroptosis, genetic/epigenetic, microbiome/metabolic) and appraises therapeutic strategies spanning surgery, hormonal suppression, assisted reproductive technologies (ART), and emerging adjuncts. Mechanistic and clinical findings are integrated to map targets, biomarkers, and precision-care opportunities across disease phenotypes. Results Evidence indicates local estrogen dominance with progesterone resistance, pervasive immune dysregulation, and oxidative stress with iron-driven ferroptosis that particularly injures granulosa cells, alongside disease-relevant genetic/epigenetic regulators and reproductive-tract/gut microbiome dysbiosis. Clinically, endometriosis detrimentally affects ovarian reserve and oocyte competence, disrupts endometrial receptivity/decidualization, and remodels pelvic anatomy through adhesions and fibrosis, cumulatively reducing fecundity. Current management includes laparoscopic excision/ablation, hormonal suppression (e.g., progestins, GnRH analogs/antagonists), and ART tailored to goals and disease severity. Adjunctive antioxidant and immune-modulating approaches show promise but require robust clinical validation. Biomarker discovery—including epigenetic regulators and microbiome-derived signals—may enable earlier diagnosis and personalization. Innovative avenues include immunotherapy targeting nociceptor–immune crosstalk, ferroptosis modulation, microbiota manipulation, and diet-based metabolic strategies. Discussion The pathogenesis of endometriosis-associated infertility is multifactorial and interconnected. While current treatments offer benefits, their efficacy is variable. The integration of multi-omics data is unveiling novel diagnostic biomarkers and therapeutic targets. Future management requires a patient-centered, multidisciplinary precision medicine approach that combines mechanistic insights with individualized treatment strategies to improve reproductive outcomes across the disease spectrum.
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