Metabolic syndrome in polycystic ovary syndrome: a systematic review, meta‐analysis and meta‐regression. (19th October 2018)

• Record Type: Journal Article
• Authors: Lim, S. S.; Kakoly, N. S.; Tan, J. W. J.; Fitzgerald, G.; Bahri Khomami, M.; Joham, A. E.; Cooray, S. D.; Misso, M. L.; Norman, R. J.; Harrison, C. L.; Ranasinha, S.; Teede, H. J.; Moran, L. J.
• Is Part Of: Obesity reviews. Volume 20:Number 2(2019)
• Page Start: 339
• Page End: 352
• Publication Date: 2018-10-19
• Subjects: meta‐analysis -- metabolic syndrome -- meta‐regression -- polycystic ovary syndrome systematic review; Obesity -- Periodicals; 616.398005
• DOI: 10.1111/obr.12762
• Languages: English
• ISSNs: 1467-7881

Abstract

Summary: Introduction: Women with polycystic ovary syndrome (PCOS) have increased risk of metabolic syndrome. The relative contribution of clinical, demographic or biochemical factors to metabolic syndrome in PCOS is not known. A literature search was conducted in MEDLINE, CINAHL, EMBASE and clinical trial registries. Of 4530 studies reviewed, 59 were included in the systematic review and 27 in the meta‐analysis and meta‐regression. In good and fair quality studies, women with PCOS had an overall increased prevalence of metabolic syndrome (odds ratio, OR 3.35, 95% confidence interval, CI 2.44, 4.59). Increased prevalence of metabolic syndrome occurred in overweight or obese women with PCOS (OR 1.88, 95% 1.16, 3.04) but not in lean women (OR 1.45, 95% CI 0.35, 6.12). In meta‐regression analyses, the markers of metabolic syndrome diagnostic criteria (waist circumference, high‐density lipoprotein cholesterol, triglyceride, blood pressure), BMI, glucose tolerance (2‐hr oral glucose tolerance test) and surrogate markers of insulin resistance (HOMA‐IR) but not markers of reproductive dysfunction (sex hormone binding globulin, testosterone, PCOS phenotypes) contributed significantly to the heterogeneity in the prevalence of metabolic syndrome. Women with PCOS have increased risk of metabolic syndrome which was associated with obesity and metabolic features but not with indices of hyperandrogenism.