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Metabolic abnormalities in young Egyptian women with polycystic ovary syndrome and their relation to <i>ADIPOQ </i>gene variants and body fat phenotype


Moushira Zaki
Shams Kholoussi
Somaia Ismail
Haiam Abdel Raouf
Iman Helwa
Naglaa Hassan
Eman Youness
Nadia A Mohamed
Sanaa Kamal
Walaa Yousef
Mohamed Shaker
Wafaa Ezzat
Yasser A Elhosary
Omnia M Saleh
Mona El Gammal
Hala T El-Bassyouni
Samira Ismail
Mamdouh Bibars
Osama Azmy

Abstract

Background: Polycystic ovary syndrome (PCOS) is the most common endocrine disorder. It is associated with high prevalence of metabolic risk factors, but little is known about the prevalence of metabolic syndrome (MS) and its components among Egyptian PCOS women. The objective of the study was to determine the metabolic abnormalities among young Egyptian women with PCOS and evaluate their relation with adiponectin gene (ADIPOQ) variants and body fat adiposity pattern.
Materials and methods: The present study included 80 PCOS women and 80 healthy women with similar age and body mass index. All participants underwent clinical, anthropometric, biochemical, ultrasonographic and adiponectin (ADIPOQ) gene 11391G>A (rs17300539) examinations. Insulin resistance was assessed by the Homeostatic model assessment for insulin resistance (HOMA-IR).
Results: MS was identified in 22.5% of PCOS women. The most prevalent MS components in PCOS women were central obesity, decreased high-density lipoprotein cholesterol (HDL-C), and increased triglycerides (TG), blood pressure (BP) and fasting glucose levels. The study found association between ADIPOQ promoter variants 11391G>A and MS in PCOS women. Moreover, multivariate logistic regression analysis showed association between abdominal fat accumulation and IR in PCOS.
Conclusion: The prevalence of MS was significantly higher in PCOS women than controls, and central obesity and hypertension are risk factors for insulin resistance. Moreover, obesity plays a key role in the development of PCOS and ADIPOQ 11391G>A gene variants showed association with MS.

KEYWORDS: ADIPOQ variants; PCOS; Metabolic syndrome; Insulin resistance; Central obesity; Young women


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eISSN: 1110-8630