151. Prevalence of metabolic syndrome in four phenotypes of PCOS and its relationship with androgenic components among Iranian women: A cross-sectional study
- Author
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Maryam Movahedinejad, Narges Zaeemzadeh, Shahideh Jahanian Sadatmahalleh, Saeideh Ziaei, Neda Mohamadzadeh, Anoshirvan Kazemnejad, and Azadeh Mottaghi
- Subjects
medicine.medical_specialty ,lcsh:QH471-489 ,Cross-sectional study ,030209 endocrinology & metabolism ,Ovary ,lcsh:Gynecology and obstetrics ,03 medical and health sciences ,0302 clinical medicine ,Insulin resistance ,Sex hormone-binding globulin ,Internal medicine ,medicine ,lcsh:Reproduction ,National Cholesterol Education Program ,lcsh:RG1-991 ,Polycystic ovary syndrome ,030219 obstetrics & reproductive medicine ,biology ,business.industry ,Hyperandrogenism ,Obstetrics and Gynecology ,polycystic ovary syndrome, metabolic syndrome, hyperandrogenism ,medicine.disease ,Metabolic syndrome ,Pathophysiology ,medicine.anatomical_structure ,Endocrinology ,Reproductive Medicine ,biology.protein ,business ,Research Article - Abstract
Background: Polycystic ovary syndrome (PCOS) increases the risk of metabolic syndrome (MetS). Insulin resistance (IR) plays a major role in the pathophysiology of both PCOS and MetS. Objective: This study was designed to compare the prevalence of MetS among different phenotypes of PCOS and its relationship with androgenic components. Materials and Methods: 182 participants eligible for this five-group comparative study were selected by convenience sampling method. They were classified according to the Rotterdam criteria: clinical and/or biochemical hyperandrogenism (H) + PCOS on ultrasound (P) + ovulation disorders (O) (n = 41), clinical and/or biochemical H + PCOS on P (n = 33), PCOS on P + O (n = 40), clinical and/or biochemical H + O (n = 37), and control (without PCOS) (n = 31). MetS was measured based on the National Cholesterol Education Program Adult Treatment Panel III criteria. Androgenic components included free androgen- index (FAI), total-testosterone (TT) level and sex-hormone-binding-globulin (SHBG). Results: A significant difference was observed between the study groups in terms of MetS prevalence (p = 0.01). In phenotype H+P+O, there was a statistically significant positive association between TG and TT, and a significant negative association between SBP and DBP with SHBG. In phenotype O+P, WC was inversely associated with SHBG. In phenotype H+O, FBS and TG were positively associated with FAI but HDL was inversely associated with FAI. Moreover, WC and DBP were positively associated with TT in phenotype H+O. No associations were detected between MetS parameters and androgenic components in other PCOS subjects (phenotype H+P) and in the control group. TT was significantly higher in the PCOS group suffering from MetS (p = 0.04). Conclusion: According to the research results, hyperandrogenic components are potent predictors of metabolic disorders. Thus, we suggest that MetS screening is required for the prevention of MetS and its related complications in PCOS women. Key words: Polycystic ovary syndrome, Metabolic syndrome, Hyperandrogenism.
- Published
- 2020