Meta-analyses of 4 CFTR variants associated with the risk of the congenital bilateral absence of the vas deferens.

Journal of clinical bioinformatics Pub Date : 2014-08-21 eCollection Date: 2014-01-01 DOI:10.1186/2043-9113-4-11
Xuting Xu, Jufen Zheng, Qi Liao, Huiqing Zhu, Hongyan Xie, Huijuan Shi, Shiwei Duan
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引用次数: 14

Abstract

Aims: The aim of our study was to evaluate the relationship between four CFTR variations and the congenital bilateral absence of the vas deferens (CBAVD).

Methods: A systematic search was performed in the literature databases for the case-control studies of CFTR variations with the risk of CBAVD. A total of 29 studies among 1139 controls and 1562 CBAVD patients were gathered for the meta-analyses of three commonly tecsted variations (5T, ΔF508 and M470V) with CBAVD.

Results: Our meta-analyses observed significant associations between CBAVD and all the three variations, including 5T (P < 0.001, OR = 8.35, 95% CI = 6.68-10.43), M470V (P = 0.027, OR = 0.74, 95% CI = 0.60-0.91) and ΔF508 (P < 0.001, OR = 22.20, 95% CI = 7.49-65.79).

Conclusion: In the current study, we demonstrated a significant association between CFTR variations and CBAVD. Our results showed that the 5T variation was a risk factor of CBAVD in French, Spanish, Japanese, Chinese, Iranian, Indian, Mexican and Egyptian populations. CFTR ΔF508 was another important risk factor in Caucasians, including Slovenians, Canadians, Iranians, and Egyptians. In addition, M470V was a protective factor among French, Chinese, Italian and Iranian populations.

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4个CFTR变异与先天性双侧输精管缺失风险相关的荟萃分析。
目的:我们的研究目的是评估四种CFTR变异与先天性双侧输精管缺失(cavd)之间的关系。方法:在文献数据库中系统检索CFTR变异与CBAVD风险的病例对照研究。共收集了29项研究,包括1139名对照和1562名CBAVD患者,对三种常见的CBAVD变异(5T、ΔF508和M470V)进行meta分析。结果:我们的荟萃分析发现,cavd与包括5T (P)在内的所有三种变异之间存在显著关联。结论:在目前的研究中,我们证明了CFTR变异与cavd之间存在显著关联。结果表明,5T变异是法国、西班牙、日本、中国、伊朗、印度、墨西哥和埃及人群发生cavd的危险因素。CFTR ΔF508是高加索人(包括斯洛文尼亚人、加拿大人、伊朗人和埃及人)的另一个重要风险因素。此外,M470V在法国、中国、意大利和伊朗人群中是一种保护因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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