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囊性纤维化跨膜传导调节因子(CFTR)基因突变及多态性与非梗阻性无精子症相关:来自病例对照研究。

CFTR gene mutations and polymorphism are associated with non-obstructive azoospermia: From case-control study.

作者信息

Jiang Lingying, Jin Jiamin, Wang Shasha, Zhang Fuxing, Dai Yongdong, Shi Libing, Zhang Songying

机构信息

Department of Gynecology and Obstetrics, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, No.3 Qingchun East Road, Jianggan District, Hangzhou, 310016, China.

Department of Gynecology and Obstetrics, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, No.3 Qingchun East Road, Jianggan District, Hangzhou, 310016, China.

出版信息

Gene. 2017 Aug 30;626:282-289. doi: 10.1016/j.gene.2017.04.044. Epub 2017 Apr 27.

Abstract

A variety of experimental studies have yielded evidence that the cystic fibrosis transmembrane conductance regulator (CFTR) protein participates in the process of spermatogenesis. However, the association between CFTR gene and non-obstructive azoospermia (NOA) disease remained to be a question. First, we reviewed available data from the PubMed and Embase databases before May 2016 to find the most common mutations of CFTR gene in NOA patients. Second, an original case-control study was conducted on NOA patients (n=100) and a control group consisting of fertile males (n=100), selected from August 2015 to March 2017, to detect CFTR gene mutations and polymorphism. Peripheral blood samples from NOA patients and normal controls were analyzed for the presence of specific sequences of CFTR gene by polymerase chain reaction amplification followed by direct sequencing. From our comprehensive review, 12 case-control studies were found concerning the relation between CFTR gene mutations and polymorphism and NOA disease. Fifty-four mutations were mentioned and IVS8 poly-T, TG repeats, F508del and R117H mutations were the most common ones. Based on that, we detected IVS8 poly-T, TG repeats, F508del, R117H and M470V mutations in our case control study. We found that the T5 allele was present at a significantly higher rate in NOA patients than in the control group (5.00% versus 0.00%, p<0.01) with increased risk having NOA [Odds ratios (OR) 2.05, 95% confidence intervals (CI) 1.85-2.27]. The T5 variant was always accompanied by TG12 (10/10) and V470 allele participated in most TG12T5 haplotypes (8/10). TG12T5-V470 haplotype also enhanced risk of having NOA [OR 2.04, 95% CI 1.84-2.26]. F508del and R117H mutations were not found in either group. In conclusion, the polyvariant mutant genes of CFTR: T5 allele and TG12-T5-V470 genotype are correlated with NOA, but F508del and R117H mutations have low possibility to be associated with NOA.

摘要

多项实验研究已得出证据表明,囊性纤维化跨膜传导调节因子(CFTR)蛋白参与精子发生过程。然而,CFTR基因与非梗阻性无精子症(NOA)疾病之间的关联仍是一个问题。首先,我们查阅了2016年5月之前来自PubMed和Embase数据库的可用数据,以找出NOA患者中CFTR基因最常见的突变。其次,对2015年8月至2017年3月期间选取的NOA患者(n = 100)和由可育男性组成的对照组(n = 100)进行了一项原始病例对照研究,以检测CFTR基因突变和多态性。通过聚合酶链反应扩增,随后直接测序,分析NOA患者和正常对照的外周血样本中CFTR基因特定序列的存在情况。通过我们的全面综述,发现了12项关于CFTR基因突变和多态性与NOA疾病之间关系的病例对照研究。提及了54种突变,其中IVS8多聚T、TG重复序列、F508del和R117H突变最为常见。基于此,我们在病例对照研究中检测了IVS8多聚T、TG重复序列、F508del、R117H和M470V突变。我们发现,NOA患者中T5等位基因的出现率显著高于对照组(5.00%对0.00%,p<0.01),患NOA的风险增加[比值比(OR)2.05,95%置信区间(CI)1.85 - 2.27]。T5变异体总是与TG12相伴出现(10/10),并且V470等位基因参与了大多数TG12T5单倍型(8/10)。TG12T5 - V470单倍型也增加了患NOA的风险[OR 2.04,95% CI 1.84 - 2.26]。两组均未发现F508del和R117H突变。总之,CFTR的多变异突变基因:T5等位基因和TG12 - T5 - V470基因型与NOA相关,但F508del和R117H突变与NOA相关的可能性较低。

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