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叶酸相关酶基因多态性与巴西特发性不育男性。

Polymorphisms in folate-related enzyme genes in idiopathic infertile Brazilian men.

机构信息

Department of Gynecology and Obstetrics, Division of Human Reproduction and Genetics, Faculdade de Medicina do ABC, Santo André, SP, Brazil.

出版信息

Reprod Sci. 2011 Dec;18(12):1267-72. doi: 10.1177/1933719111411729. Epub 2011 Jul 20.

Abstract

The aim of the study was to analyze the distribution of the methylenetetrahydrofolate reductase (MTHFR), methionine synthase reductase (MTRR), and methionine synthase (MTR) polymorphisms in idiopathic infertile Brazilian men and fertile men. Case-control study comprising 133 idiopathic infertile Brazilian men with nonobstructive azoospermia ([NOA] n = 55) or severe oligozoospermia ([SO] n = 78) and 173 fertile men as controls. MTHFR C677T, A1298C, and G1793A; MTRR A66G; and MTR A2756G polymorphisms were studied by quantitative polymerase chain reaction (qPCR). The results were analyzed statistically and a P value <.05 was considered significant. Single-marker analysis revealed a significant association among MTHFR C677T polymorphism and both NOA group (P = .018) and SO group (P < .001). Considering the MTHFR A1298C, MTHFR G1793A, and MTRR A66G polymorphisms, no difference was found between NOA group and SO group. Regarding the MTR A2756G polymorphism, a significant difference was found between NOA and controls, P = .017. However, statistical analysis revealed no association between SO group and controls. Combined genotypes of 3 MTHFR polymorphisms did not identify a haplotype associated with idiopathic infertility. The combinatory analysis of the 3 polymorphisms MTHFR, MTRR, and MTR did not show difference between cases and controls. The findings suggest the MTHFR C677T and MTR A2756G polymorphisms could be an important genetic factor predisposing to idiopathic infertility in Brazilian men.

摘要

这项研究的目的是分析亚甲基四氢叶酸还原酶(MTHFR)、甲硫氨酸合成酶还原酶(MTRR)和甲硫氨酸合成酶(MTR)多态性在巴西特发性不孕男性和生育男性中的分布。该研究采用病例对照设计,共纳入 133 名巴西特发性不育男性,其中非梗阻性无精子症(NOA)患者 55 例,严重少精子症(SO)患者 78 例,并选择 173 名生育男性作为对照。采用实时定量聚合酶链反应(qPCR)方法检测 MTHFR C677T、A1298C 和 G1793A、MTRR A66G 以及 MTR A2756G 多态性。对结果进行统计学分析,P 值 <.05 为差异有统计学意义。单标记分析显示,MTHFR C677T 多态性与 NOA 组(P =.018)和 SO 组(P <.001)均显著相关。对于 MTHFR A1298C、MTHFR G1793A 和 MTRR A66G 多态性,NOA 组与 SO 组之间无差异。关于 MTR A2756G 多态性,NOA 组与对照组之间存在显著差异(P =.017)。然而,SO 组与对照组之间的统计学分析并未显示出相关性。3 个 MTHFR 多态性的组合基因型并未鉴定出与特发性不育相关的单倍型。3 个多态性 MTHFR、MTRR 和 MTR 的组合分析未显示病例组和对照组之间存在差异。研究结果表明,MTHFR C677T 和 MTR A2756G 多态性可能是巴西男性特发性不育的一个重要遗传因素。

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