DEVELOPMENT OF PERSONALIZED, NON-HORMONAL, AI- DRIVEN TREATMENT PATHWAYS FOR HEAVY MENSTRUAL BLEEDING BASED ON MENSTRUAL BLOOD BIOMARKERS AND UTERINE MICROBIOME PROFILING
DOI:
https://doi.org/10.64105/g7fwcm77Abstract
Heavy menstrual bleeding (HMB) is a prevalent gynecological issue that disproportionately affects women in South Asia, contributing to high rates of anemia and diminished quality of life 1 2 . Conventional therapies, often hormone-based or surgical, are not universally acceptable and fail to account for individual etiological differences. Recent advances in menstrual blood biomarker discovery and uterine microbiome profiling offer opportunities for precision medicine approaches to HMB. This study presents a comprehensive overview of HMB in the South Asian context and proposes a novel framework for personalized, non-hormonal, AI-driven treatment pathways. We review real-time clinical trial data and current evidence on key menstrual blood biomarkers (e.g., prostaglandin E2, inflammatory cytokines, fibrinolytic factors) and uterine microbiome patterns (e.g., Lactobacillus deficiency, enriched anaerobic taxa) associated with HMB 3 4 . An experimental methodology is outlined whereby patient-specific biomarker and microbiome profiles inform an artificial intelligence (AI) model to recommend tailored interventions – for example, antifibrinolytics for hyperfibrinolytic phenotypes or targeted antibiotics for microbiome dysbiosis –thereby avoiding blanket hormonal therapy. A proof-of- concept framework (Figure 1) illustrates integration of clinical data with machine learning to optimize treatment selection in real time. The clinical relevance of this personalized approach is emphasized, aiming to improve outcomes and patient satisfaction in low-resource settings. This manuscript underscores the novelty of combining “omics” data with AI in HMB management, and discusses the potential benefits and challenges of implementing such personalized, non-hormonal treatment pathways in South Asia.
Keywords: Heavy menstrual bleeding; Personalized medicine; Menstrual blood biomarkers; Uterine microbiome; Non-hormonal treatment; Artificial intelligence; South Asia




