首页> 美国卫生研究院文献>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:黄体化激素绒毛膜促性腺激素受体基因多态性(rs2293275)与多囊卵巢综合征的关联。

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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:根据雄激素过多协会–2006年多囊卵巢综合征(PCOS)的标准,多囊卵巢和月经/排卵不规律是高雄激素血症的重要诊断标准。在PCOS的发病机制中,导致卵巢衰竭的候选基因之一是促黄体生成激素(LH)绒毛膜促性腺激素受体(LHCGR)。我们的目的是研究研究人群中LHCGR多态性(rs2293275)与PCOS的关联。材料和方法:来自印度南部大都市海得拉巴多个妇科中心的遗传病例对照研究。该研究纳入了204名患有PCOS的女性以及204名健康,性别和年龄匹配的对照。在精心设计的备考中获得了人体测量和生化特征。使用聚合酶链反应-限制性片段长度多态性方法,然后进行12%聚丙烯酰胺凝胶电泳,对整个研究人群进行了脱氧核糖核酸(DNA)的分离和基因型分析。结果:在这项研究中,我们证明了LHCGR(rs2293275)多态性与PCOS之间存在关联。 G等位基因在PCOS中的频率为0.60,在对照中为0.49(几率[OR] 1.531,置信区间[CI] 1.16–2.01,p值= 0.0026),这表明G等位基因与PCOS中的PCOS相关。我们的人口。 GG基因型具有显着发展为PCOS的风险(OR 3.36,CI 1.96–5.75,p值<0.0001)。与对照组相比,我们发现PCOS中GG等位基因与体重指数,腰臀比,胰岛素抵抗,LH和LH /促卵泡激素(FSH)比率显着相关。 AA等位基因显示高的基础FSH水平。结论:这项研究表明,LHCGR(rs2293275)多态性与PCOS相关,并且可以用作相关的分子标记物,以鉴定在我们的人群中有罹患PCOS风险的女性,并且可以提供有关PCOS病因的认识。

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