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GSTM1 和 GSTT1 缺失多态性与男性不育风险:一项包含 6934 例的更新荟萃分析。

GSTM1 and GSTT1 null polymorphisms and male infertility risk: an updated meta-analysis encompassing 6934 subjects.

机构信息

State Key Laboratory of Reproductive Medicine, Wuxi Maternity and Child Health Care Hospital Affiliated to Nanjing Medical University, Wuxi 214002, China.

出版信息

Sci Rep. 2013;3:2258. doi: 10.1038/srep02258.

Abstract

Published data on the association between the GST genes polymorphisms and male infertility risk are inconclusive. We investigated GST genes polymorphisms in a large sample size case-control study, and conducted a literature-based meta-analysis of 6934 individuals. Our case-control study showed the GSTM1 null genotype was significantly associated with idiopathic oligozoospermia, while the null genotype of GSTT1 was significantly associated with normozoospermia and azoospermia. Additionally, significantly elevated GSTT1 expression levels were observed in present genotype compared with null genotype. In the meta-analysis, the null genotype of GSTM1 was associated with a significantly increased risk of male infertility. Furthermore, a stratification analysis showed that the risk of GSTM1 polymorphism was associated with male infertility in both Asian and Caucasian groups. Further studies of GSTM1 and GSTT1 with their biological functions are needed to understand the role of these genes in the development of male infertility.

摘要

关于 GST 基因多态性与男性不育风险之间的关联,已有发表的数据尚无定论。我们在一项大样本病例对照研究中调查了 GST 基因多态性,并对 6934 个人进行了基于文献的荟萃分析。我们的病例对照研究表明,GSTM1 缺失基因型与特发性少精子症显著相关,而 GSTT1 缺失基因型与正常精子症和无精子症显著相关。此外,与缺失基因型相比,GSTT1 的表达水平在现有基因型中显著升高。在荟萃分析中,GSTM1 的缺失基因型与男性不育的风险显著增加相关。此外,分层分析表明,GSTM1 多态性的风险与亚洲和白种人群的男性不育有关。需要进一步研究 GSTM1 和 GSTT1 及其生物学功能,以了解这些基因在男性不育症发展中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cb6/6505401/d0a24d60e274/srep02258-f1.jpg

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