首页> 外文期刊>Molecular reproduction and development >The Role of Endothelial Nitric Oxide Synthase (eNOS) T-786C, G894T, and 4a/b Gene Polymorphisms in the Risk of Idiopathic Male Infertility
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The Role of Endothelial Nitric Oxide Synthase (eNOS) T-786C, G894T, and 4a/b Gene Polymorphisms in the Risk of Idiopathic Male Infertility

机译:内皮型一氧化氮合酶(eNOS)T-786C,G894T和4a / b基因多态性在特发性男性不育风险中的作用

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A considerable number of infertile men have no known mechanism for their infertility. This study aims to examine if there is an association between endothelial nitric oxide synthase (eNOS) T-786C, G894T, and 4a/b gene polymorphisms and idiopathic male infertility. Three hundred fifty-two men with idiopathic infertility (mean age 32.4 +/- 11.4 years) and 356 healthy controls (mean age 33.2 +/- 11.6 years) with documented fertility were recruited in this study. Genotypes for T-786C, G894T, and 4a/b gene polymorphisms were identified by the polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) analysis. The eNOS -786CC genotype (0.310 vs. 0.081; odds ratio (OR), 3.64; 95% confidence interval (Cl), 2.28-4.46; P = 0.001), 894TT genotype (0.131 vs. 0.006; OR, 3.62; 95% Cl, 2.68-4.87; P = 0.001) and 4aa genotype (0.128 vs. 0.009; OR, 2.82; 95% Cl, 1.88-3.89; P = 0.004) were significantly more frequent in infertile subjects. Furthermore, there was a significant difference between the group of infertile patients with azoospermia and oligoasthenoteratozoospermia (OAT) when compared by genotype distribution (-786CC vs. 786TT, 894TT vs. 894GG, and 4aa vs. 4bb) (all P < 0.01). We also found an association between the eNOS "-786C," "894T," and "a" alleles and an increased risk of poor semen parameters. Our data revealed a significant relationship between eNOS genotypes and the phenotype of infertility.
机译:相当多的不育男性对其不育症没有已知的机制。这项研究旨在检查内皮一氧化氮合酶(eNOS)T-786C,G894T和4a / b基因多态性与特发性男性不育之间是否存在关联。在这项研究中,招募了三百五十二位患有特发性不育的男性(平均年龄为32.4 +/- 11.4岁)和356名健康对照(平均年龄为33.2 +/- 11.6岁)。通过聚合酶链反应限制片段长度多态性(PCR-RFLP)分析鉴定了T-786C,G894T和4a / b基因多态性的基因型。 eNOS -786CC基因型(0.310 vs.0.081;比值比(OR),3.64; 95%置信区间(Cl),2.28-4.46; P = 0.001),894TT基因型(0.131 vs.0.006; OR,3.62; 95% Cl,2.68-4.87; P = 0.001)和4aa基因型(0.128 vs.0.00; OR,2.82; 95%Cl,1.88-3.89; P = 0.004)在不育症患者中更为频繁。此外,按基因型分布比较(-786CC vs.786TT,894TT vs.894GG和4aa vs.4bb)时,无精子症无精症患者和少突性少精子症(OAT)患者之间存在显着差异(所有P <0.01)。我们还发现eNOS“ -786C”,“ 894T”和“ a”等位基因与精液参数差的风险增加有关。我们的数据揭示了eNOS基因型与不育表型之间的显着关系。

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