Predictive markers of endometriosis: a future perspective
This review synthesizes evidence on emerging genetic, epigenetic, and clinical factors as predictive markers for endometriosis, highlighting their potential for risk stratification and preventive strategies.
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This narrative review examines emerging predictive markers for endometriosis, focusing on how genetic and epigenetic alterations and clinical features such as dysmenorrhea, migraine, autoimmune and endocrine disorders, and stress or early-life adversity have been linked to disease initiation, lesion development, and symptom severity. The authors describe endometriosis as a multifactorial condition with shared genetic and molecular pathways with other chronic pain and inflammatory disorders, and they synthesize evidence supporting the need for multimodal risk stratification that considers interactions among candidate markers. A key limitation acknowledged is that, despite progress, large prospective studies are still required to validate these biomarkers and enable targeted interventions. This paper is centrally about endometriosis — it synthesizes current evidence on predictive biomarkers and future validation needs for risk stratification in endometriosis.
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