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Estrogen receptor αlpha gene (ESR1) PvuII and XbaI polymorphisms are associated to metabolic and proinflammatory factors in polycystic ovary syndrome

pmid: 25617525
Estrogen receptor αlpha gene (ESR1) PvuII and XbaI polymorphisms are associated to metabolic and proinflammatory factors in polycystic ovary syndrome
Polycystic ovary syndrome (PCOS) is a complex endocrine disorder that involves multiple factors. Although the etiology of PCOS is unknown, there is an involvement of sex steroid hormones in the pathophysiology of this syndrome. Therefore, polymorphisms in genes involved in the action of estrogen may contribute to a woman's susceptibility to PCOS.This study aimed to evaluate the association between the polymorphisms PvuII and XbaI in the estrogen receptor alpha (ESR1) gene and the occurrence of PCOS. The study also aimed to assess the influence of these polymorphisms on the metabolic and inflammatory profiles of women with PCOS.This case-control study included 99 women with PCOS, diagnosed according to the Rotterdam criteria, and 104 age-matched healthy women. The polymorphisms were evaluated using polymerase chain reaction-restriction fragment length polymorphism.No association between the ESR1 gene polymorphisms and the presence of PCOS was observed. However, we found associations between the PvuII polymorphism and C-reactive protein levels, testosterone levels, family history of diabetes, and waist circumference. The XbaI polymorphism was associated with fasting glucose and a family history of hypertension.These polymorphisms are not associated with PCOS development, but they are involved in the phenotype of complications of the syndrome. Therefore, prior knowledge of these genomic variants might contribute to taking preventive measures that could delay the metabolic and reproductive complications commonly seen in women with PCOS.
Adult, Blood Glucose, DNA-Cytosine Methylases, Estrogen Receptor alpha, Middle Aged, Young Adult, C-Reactive Protein, Case-Control Studies, Humans, Female, Genetic Predisposition to Disease, Inflammation Mediators, Insulin Resistance, Deoxyribonucleases, Type II Site-Specific, Genetic Association Studies, Polymorphism, Restriction Fragment Length, Polycystic Ovary Syndrome
Adult, Blood Glucose, DNA-Cytosine Methylases, Estrogen Receptor alpha, Middle Aged, Young Adult, C-Reactive Protein, Case-Control Studies, Humans, Female, Genetic Predisposition to Disease, Inflammation Mediators, Insulin Resistance, Deoxyribonucleases, Type II Site-Specific, Genetic Association Studies, Polymorphism, Restriction Fragment Length, Polycystic Ovary Syndrome
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