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首页> 外文期刊>Genetic testing and molecular biomarkers >Association of Luteinizing Hormone Chorionic Gonadotropin Receptor Gene Polymorphism (rs2293275) with Polycystic Ovarian Syndrome
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Association of Luteinizing Hormone Chorionic Gonadotropin Receptor Gene Polymorphism (rs2293275) with Polycystic Ovarian Syndrome

机译:促黄体激素绒毛膜协会促性腺激素受体基因多态性(rs2293275)和多囊性卵巢综合征

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摘要

Background: Polycystic ovaries and irregular menstruation/anovulation are important diagnostic criteria along with hyperandrogenism as per the Androgen Excess Society-2006 criteria for polycystic ovarian syndrome (PCOS). In the etiopathogenesis of PCOS, one of the candidate genes causing ovarian failure is the luteinizing hormone (LH) chorionic gonadotropin hormone receptor (LHCGR). Our aim was to study the association of LHCGR polymorphism (rs2293275) with PCOS in our study population. Materials and Methods: Genetic case-control study from multiple gynecological centers from Hyderabad, a cosmopolitan city in South India. The study involved 204 women with PCOS and 204 healthy, sex-, and age-matched controls. Anthropometric and biochemical profiles were taken in a well-designed pro forma. Isolation of deoxyribonucleic acid (DNA) and genotype analysis were done for the entire study population using the polymerase chain reaction-restriction fragment length polymorphism method followed by 12% polyacrylamide gel electrophoresis. Results: In this study, we have demonstrated an association between LHCGR (rs2293275) polymorphism and PCOS. The frequency of the G allele was 0.60 in PCOS and 0.49 in controls (odds ratio [OR] 1.531, confidence interval [CI] 1.16-2.01, and p-value=0.0026), which indicates that the G allele is associated with PCOS in our population. The GG genotype conferred a significant risk of developing PCOS (OR 3.36, CI 1.96-5.75, and p-value<0.0001). We found a significant association of the GG allele with body-mass index, waist to hip ratio, insulin resistance, LH, and LH/follicle-stimulating hormone (FSH) ratio in PCOS when compared with controls. The AA allele showed high basal FSH levels. Conclusions: This study suggests that LHCGR (rs2293275) polymorphism is associated with PCOS and could be used as a relevant molecular marker to identify women with the risk of developing PCOS in our population and may provide an understanding about the etiology of PCOS.
机译:背景:多囊卵巢和不规则的月经/停止排卵的诊断很重要标准与雄激素过多症的雄激素过多的社会- 2006标准多囊卵巢综合征(PCOS)。多囊卵巢综合征的发病机理,候选人之一基因导致卵巢黄体化失败激素(LH)绒毛膜促性腺激素激素受体(LHCGR)。协会LHCGR多态性(rs2293275)人口与PCOS在我们的研究中。方法:从多个遗传病例对照研究妇科中心从海德拉巴在印度南部的大都市。患多囊卵巢综合征的204名女性和204名健康,性别和年龄组。和生化概要文件中精心设计的形式上。脱氧核糖核酸(DNA)和基因型分析完成了整个研究人群使用在聚合酶链reaction-restriction片段长度多态性方法紧随其后12%的聚丙烯酰胺凝胶电泳。在这项研究中,我们演示了一个联系LHCGR (rs2293275)多态性和多囊卵巢综合征。等位基因在控制PCOS的0.60和0.49(优势比1.531[或],可信区间[CI]1.16 - -2.01, p = 0.0026)G等位基因是与PCOS中有关人口。重大的风险PCOS(或3.36,CI1.96 - -5.75, p值< 0.0001)。重要的协会GG等位基因体重指数、腰臀比、胰岛素电阻、LH、LH /促卵泡激素(FSH)比率在PCOS相比控制。的水平。LHCGR (rs2293275)多态性与PCOS,可以作为相关分子标志识别的风险的女性我国人口发展PCOS可能提供一个了解多囊卵巢综合征的病因。

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