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

机译:GSTM1和GSTT1无效多态性与男性不育风险:涵盖6934名受试者的最新荟萃分析

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摘要

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.
机译:有关GST基因多态性与男性不育风险之间关系的公开数据尚无定论。我们在一个大样本量的病例对照研究中调查了GST基因多态性,并对6934个个体进行了基于文献的荟萃分析。我们的病例对照研究表明,GSTM1无效基因型与特发性少精子症显着相关,而GSTT1无效基因型与正常精子症和无精子症显着相关。另外,与无效基因型相比,在当前基因型中观察到了显着升高的GSTT1表达水平。在荟萃分析中,GSTM1的无效基因型与男性不育风险显着增加有关。此外,分层分析显示,亚洲和白种人组中GSTM1多态性的风险与男性不育有关。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。

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