Cardio-metabolic risk in Rotterdam clinical phenotypes of PCOS

被引:2
|
作者
Mitra, Subarna [1 ]
Saharia, Gautom K. [2 ]
Jena, Saubhagya K. [1 ]
机构
[1] All India Inst Med Sci, Dept Obstet & Gynecol, Bhubaneswar 751019, Odisha, India
[2] All India Inst Med Sci, Dept Biochem, Bhubaneswar 751019, Odisha, India
关键词
Anti-Mullerian hormone; Cardio-metabolic risk; Polycystic ovary syndrome; Rotterdam phenotypes; POLYCYSTIC-OVARY-SYNDROME; ANTI-MULLERIAN HORMONE; INSULIN-RESISTANCE; MAIN PHENOTYPES; CRITERIA; WOMEN; ENDOCRINE; CONSENSUS; SEVERITY; OBESITY;
D O I
10.1016/j.ando.2023.06.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and aims. - Elevated anti-Mullerian hormone (AMH) in polycystic ovary syndrome (PCOS) characterizes the clinical severity of the 4 phenotypes; but whether it also reflects the corresponding differences in cardio-metabolic risk remains to be elucidated. This study aimed to compare metabolic profile between the 4 clinical phenotypes of PCOS and to determine the influence of AMH levels on metabolic severity. Methods. - One hundred and forty-four women with PCOS, aged between 20 and 40 years, were recruited in this cross-sectional study and categorized according to the 4 phenotypes of the Rotterdam criteria. Anthropometry and blood pressure were recorded. Fasting lipid profile, fasting glucose, fasting insulin, homeostasis model assessment insulin resistance, total testosterone and AMH were estimated. Clinical, anthropometric and metabolic profiles were compared between the 4 phenotypes. Results. - There were significant differences in menstrual abnormalities, weight, hip circumference, clinical hyperandrogenism, ovarian volume and AMH levels between the 4 phenotypes. Cardio-metabolic risk factors and rates of metabolic syndrome (MS) and insulin resistance (IR) were comparable. Conclusion. - Cardio-metabolic risk is similar in all phenotypes of PCOS despite differences in anthropometry and AMH levels. All women diagnosed with PCOS should undergo screening and lifelong surveillance for MS, IR and cardiovascular diseases, irrespective of clinical phenotype or AMH level. This needs further validation in prospective multi -center studies across the country, with larger sample sizes and adequate power. (c) 2023 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:44 / 47
页数:4
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