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基于全基因组关联研究的血清性激素水平。

Genome-wide association studies on serum sex steroid levels.

机构信息

Centre for Bone and Arthritis Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Centre for Bone and Arthritis Research, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

出版信息

Mol Cell Endocrinol. 2014 Jan 25;382(1):758-766. doi: 10.1016/j.mce.2013.03.009. Epub 2013 Mar 28.

Abstract

Even though the levels of circulating sex steroid hormones are to a large extent heritable, their genetic determinants are largely unknown. With the advent of genome-wide association studies (GWAS), much progress has been made and several genetic loci have been identified to be associated with serum levels of dehydroepiandrosterone sulfate, testosterone and sex hormone-binding globulin. The variants identified so far only explain a small amount of the overall heritability, but may help to elucidate the role of sex steroid hormones in common disorders such as hypogonadism, type 2 diabetes and hormone-sensitive cancers. This review provides an overview of the current state of knowledge of the genetic determinants of sex steroid hormones, with a focus on recent GWAS and brief directions for elucidating the remaining heritability.

摘要

尽管循环性激素水平在很大程度上是可遗传的,但它们的遗传决定因素在很大程度上仍是未知的。随着全基因组关联研究(GWAS)的出现,已经取得了很大的进展,已经确定了几个与硫酸脱氢表雄酮、睾酮和性激素结合球蛋白的血清水平相关的遗传位点。迄今为止确定的变异体仅能解释整体遗传率的一小部分,但可能有助于阐明性激素在常见疾病(如性腺功能减退症、2 型糖尿病和激素敏感性癌症)中的作用。这篇综述概述了性激素遗传决定因素的最新知识状态,重点介绍了最近的 GWAS,并简要介绍了阐明剩余遗传率的方向。

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