Biochemical and Metabolic Disruptions in Endometriosis
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Abstract
Objectives:Endometriosis is a chronic gynecological disorder characterized by endometrial glands and stroma outside the uterine cavity. This study aims to characterize biochemical, hormonal, and inflammatory alterations in endometriosis, with the goal of gaining insights into disease mechanisms and exploring candidate biomarkers that could inform future studies on early diagnosis or targeted interventions.
Materials And Methods: A case-control study enrolled 300 participants aged 20 to 45 years, including 150 individuals diagnosed with endometriosis and 150 healthy controls recruited from hospitals across Thiruvananthapuram. Serum interleukin-6 (IL-6), prolactin, luteinizing hormone (LH), and follicle-stimulating hormone (FSH) were measured using enzyme-linked immunosorbent assay (ELISA), while triiodothyronine (T3), thyroxine (T4), and thyroid-stimulating hormone (TSH) were analyzed via chemiluminescent immunoassay (CLIA). Metabolic parameters were assessed using a semi-automated analyzer.
Results: Findings suggest that women with endometriosis had significantly higher body mass index (BMI), abdominal circumference, fasting blood sugar (FBS), triglycerides, low-density lipoprotein (LDL), IL-6, TSH, prolactin, and FSH, while high-density lipoprotein (HDL), T3, T4, and LH levels were lower (p ≤ 0.05). Clinical conditions such as diabetes mellitus, dyslipidemia, thyroid disorders, polycystic ovary syndrome (PCOS), and psychological stress were more prevalent in cases. Receiver operating characteristic (ROC) analysis identified prolactin and IL-6 as the strongest diagnostic predictors, while multivariable analysis confirmed BMI, abdominal circumference, prolactin, and IL-6 as key factors associated with endometriosis.
Conclusion:This study reveals key biochemical and metabolic disruptions in endometriosis, linking obesity, PCOS, and stress to disease progression, and highlights potential biomarkers for early diagnosis and targeted treatment.
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