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内皮型一氧化氮合酶(eNOS)T-786C、4a4b及G894T基因多态性与男性不育:特发性弱精子症的研究及荟萃分析

Endothelial nitric oxide synthase (eNOS) T-786C, 4a4b, and G894T polymorphisms and male infertility: study for idiopathic asthenozoospermia and meta-analysis.

作者信息

Song Pingping, Zou Shasha, Chen Tingting, Chen Jianhua, Wang Yanan, Yang Juanjuan, Song Zhijian, Jiang Huayu, Shi Huijuan, Huang Yiran, Li Zheng, Shi Yongyong, Hu Hongliang

机构信息

Department of Urology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, P.R. China.

BIO-X Center, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai, Peoples Republic of China.

出版信息

Biol Reprod. 2015 Feb;92(2):38. doi: 10.1095/biolreprod.114.123240. Epub 2014 Dec 10.

Abstract

Recent studies on the eNOS gene and male infertility show that expression of eNOS regulates normal spermatogenesis in the testis, and the eNOS gene variants (T-786C, 4a4b, and G894T) are potentially involved in impairment of spermatogenesis and sperm function. Thus, we conducted this association and meta-analysis study to further validate whether variants of those three loci affected the risk of idiopathic asthenozoospermia (AZS) and male infertility. Approximately 340 Chinese idiopathic AZS patients and 342 healthy men were included for this case-control study, genotyped by gel electrophoresis analysis or direct sequencing of PCR products. The eNOS mRNA isolated from the semen of patients was further examined by quantitative real-time PCR. Also, a meta-analysis of association between eNOS gene polymorphisms and male infertility was performed. A significant association was identified on allelic level between 4a4b variant and AZS in our study (chi-squared = 7.53, corrected P = 0.018, odds ratio (OR) = 1.808), while there were no significant difference of T-786C and G894T for asthenozoospermia in both genotype and allele distributions. In addition, expression of eNOS was up-regulated in patients compared with controls (about 2.4-fold, P < 0.001). Furthermore, the results of the meta-analysis support the conclusion that the T-786C and 4a4b loci were associated with male infertility in both Asian and Caucasian populations. Our study provides genetic evidence for the eNOS gene being a risk factor for idiopathic AZS and male infertility. Considering genetic differences among populations and complex pathogenesis of male infertility, more validating studies using independent samples are suggested in the future.

摘要

近期关于内皮型一氧化氮合酶(eNOS)基因与男性不育的研究表明,eNOS的表达调控睾丸中的正常精子发生,且eNOS基因变异体(T-786C、4a4b和G894T)可能参与精子发生和精子功能的损害。因此,我们开展了这项关联和荟萃分析研究,以进一步验证这三个位点的变异是否影响特发性弱精子症(AZS)和男性不育的风险。本病例对照研究纳入了约340例中国特发性AZS患者和342名健康男性,通过凝胶电泳分析或PCR产物直接测序进行基因分型。从患者精液中分离的eNOS mRNA通过定量实时PCR进一步检测。此外,还对eNOS基因多态性与男性不育之间的关联进行了荟萃分析。在我们的研究中,在等位基因水平上发现4a4b变异体与AZS之间存在显著关联(卡方 = 7.53,校正P = 0.018,比值比(OR) = 1.808),而T-786C和G894T在弱精子症的基因型和等位基因分布方面均无显著差异。此外,与对照组相比,患者中eNOS的表达上调(约2.4倍,P < 0.001)。此外,荟萃分析结果支持T-786C和4a4b位点在亚洲和白种人群中均与男性不育相关的结论。我们的研究为eNOS基因是特发性AZS和男性不育的危险因素提供了遗传学证据。考虑到人群之间的遗传差异以及男性不育的复杂发病机制,建议未来使用独立样本进行更多的验证研究。

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