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中国男性性激素、促性腺激素和性激素结合蛋白的全基因组关联研究。

Genome-wide association study of sex hormones, gonadotropins and sex hormone-binding protein in Chinese men.

机构信息

Center for Cancer Genomics, Wake Forest University School of Medicine, Winston-Salem, North Carolina, USA.

出版信息

J Med Genet. 2013 Dec;50(12):794-801. doi: 10.1136/jmedgenet-2013-101705. Epub 2013 Sep 18.

Abstract

BACKGROUND

Sex hormones and gonadotropins exert a wide variety of effects in physiological and pathological processes. Accumulated evidence shows a strong heritable component of circulating concentrations of these hormones. Recently, several genome-wide association studies (GWASs) conducted in Caucasians have identified multiple loci that influence serum levels of sex hormones. However, the genetic determinants remain unknown in Chinese populations. In this study, we aimed to identify genetic variants associated with major sex hormones, gonadotropins, including testosterone, oestradiol, follicle-stimulating hormone (FSH), luteinising hormone (LH) and sex hormone binding globulin (SHBG) in a Chinese population.

METHODS

A two-stage GWAS was conducted in a total of 3495 healthy Chinese men (1999 subjects in the GWAS discovery stage and 1496 in the confirmation stage).

RESULTS

We identified a novel genetic region at 15q21.2 (rs2414095 in CYP19A1), which was significantly associated with oestradiol and FSH in the Chinese population at a genome-wide significant level (p=6.54×10(-31) and 1.59×10(-16), respectively). Another single nucleotide polymorphism in CYP19A1 gene was significantly associated with oestradiol level (rs2445762, p=7.75×10(-28)). In addition, we confirmed the previous GWAS-identified locus at 17p13.1 for testosterone (rs2075230, p=1.13×10(-8)) and SHBG level (rs2075230, p=4.75×10(-19)) in the Chinese population.

CONCLUSIONS

This study is the first GWAS investigation of genetic determinants of FSH and LH. The identification of novel susceptibility loci may provide more biological implications for the synthesis and metabolism of these hormones. More importantly, the confirmation of the genetic loci for testosterone and SHBG suggests common genetic components shared among different ethnicities.

摘要

背景

性激素和促性腺激素在生理和病理过程中发挥着广泛的作用。有大量证据表明,这些激素的循环浓度具有很强的遗传性。最近,在白种人群中进行的几项全基因组关联研究(GWAS)已经确定了多个影响性激素血清水平的基因座。然而,这些遗传决定因素在中国人中尚不清楚。在这项研究中,我们旨在鉴定与主要性激素、促性腺激素(包括睾酮、雌二醇、卵泡刺激素(FSH)、黄体生成素(LH)和性激素结合球蛋白(SHBG)相关的遗传变异在中国人群中的作用。

方法

在总共 3495 名健康中国男性(GWAS 发现阶段 1999 名受试者,确认阶段 1496 名)中进行了两阶段 GWAS。

结果

我们在中国人中发现了一个新的遗传区域 15q21.2(CYP19A1 中的 rs2414095),该区域与雌二醇和 FSH 显著相关,达到全基因组显著水平(分别为 p=6.54×10(-31)和 1.59×10(-16))。CYP19A1 基因中的另一个单核苷酸多态性与雌二醇水平显著相关(rs2445762,p=7.75×10(-28))。此外,我们还证实了先前在 17p13.1 上发现的与睾酮(rs2075230,p=1.13×10(-8))和 SHBG 水平(rs2075230,p=4.75×10(-19))相关的 GWAS 鉴定的基因座在中国人中。

结论

本研究是对 FSH 和 LH 遗传决定因素的首次 GWAS 研究。新的易感基因座的鉴定可能为这些激素的合成和代谢提供更多的生物学意义。更重要的是,对睾酮和 SHBG 遗传基因座的确认表明不同种族之间存在共同的遗传成分。

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