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Cardio-metabolic risk in Rotterdam clinical phenotypes of PCOS - 22/02/24

Doi : 10.1016/j.ando.2023.06.001 
Subarna Mitra a, , Gautom K. Saharia b, Saubhagya K. Jena a
a Department of Obstetrics and Gynecology, All India Institute of Medical Sciences, Bhubaneswar, 751019 Odisha, India 
b Department of Biochemistry, All India Institute of Medical Sciences, Bhubaneswar, 751019 Odisha, India 

Corresponding author at: Department of Obstetrics and Gynecology, All India Institute of Medical Sciences, Sijua, Patrapada, Bhubaneswar, 751019 Odisha, India.Department of Obstetrics and Gynecology, All India Institute of Medical Sciences, Sijua, Patrapada, BhubaneswarOdisha751019India

Abstract

Background and aims

Elevated anti-Müllerian 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 40years, 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.

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Keywords : Anti-Müllerian hormone, Cardio-metabolic risk, Polycystic ovary syndrome, Rotterdam phenotypes


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Vol 85 - N° 1

P. 44-47 - février 2024 Regresar al número
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