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黄体生成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

Association of luteinizing hormone chorionic gonadotropin receptor gene polymorphism (rs2293275) with polycystic ovarian syndrome.

作者信息

Thathapudi Sujatha, Kodati Vijayalakshmi, Erukkambattu Jayashankar, Addepally Uma, Qurratulain Hasan

机构信息

1 Department of Genetics and Molecular Medicine, Vasavi Medical and Research Center , Hyderabad, India .

出版信息

Genet Test Mol Biomarkers. 2015 Mar;19(3):128-32. doi: 10.1089/gtmb.2014.0249. Epub 2015 Jan 7.

Abstract

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.

摘要

背景

根据雄激素过多协会2006年多囊卵巢综合征(PCOS)的诊断标准,多囊卵巢以及月经不规律/无排卵是重要的诊断标准,同时伴有高雄激素血症。在PCOS的病因发病机制中,导致卵巢功能衰竭的候选基因之一是促黄体生成素(LH)绒毛膜促性腺激素受体(LHCGR)。我们的目的是在我们的研究人群中研究LHCGR基因多态性(rs2293275)与PCOS的关联。

材料与方法

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例PCOS女性患者以及204例年龄、性别匹配的健康对照。通过精心设计的表格记录人体测量和生化指标。使用聚合酶链反应-限制性片段长度多态性方法,随后进行12%聚丙烯酰胺凝胶电泳,对整个研究人群进行脱氧核糖核酸(DNA)分离和基因分型分析。

结果

在本研究中,我们证明了LHCGR(rs2293275)基因多态性与PCOS之间存在关联。PCOS患者中G等位基因的频率为0.60,对照组为0.49(优势比[OR]1.531,置信区间[CI]1.16 - 2.01,p值 = 0.0026),这表明在我们的人群中G等位基因与PCOS相关。GG基因型赋予了发生PCOS的显著风险(OR 3.36,CI 1.96 - 5.75,p值<0.0001)。与对照组相比,我们发现PCOS患者中GG等位基因与体重指数、腰臀比、胰岛素抵抗、LH以及LH/促卵泡生成素(FSH)比值之间存在显著关联。AA等位基因显示基础FSH水平较高。

结论

本研究表明,LHCGR(rs2293275)基因多态性与PCOS相关,可作为识别我们人群中具有发生PCOS风险女性的相关分子标志物,并可能有助于了解PCOS的病因。

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