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首页> 外文期刊>International Journal of Clinical and Experimental Medicine >XPD Asp312Asn polymorphism and esophageal cancer risk: an update meta-analysis based on 3928 cases and 6012 controls
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XPD Asp312Asn polymorphism and esophageal cancer risk: an update meta-analysis based on 3928 cases and 6012 controls

机译:XPD Asp312Asn基因多态性与食管癌风险:基于3928例病例和6012例对照的最新荟萃分析

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Background: Although xeroderma pigmentosum group D (XPD) was reported to be related with esophageal cancer (EC) risk, the results remained inconsistent. The aim of this meta-analysis was to make a more precise estimation of the relationship between XPD Asp312Asn polymorphism and EC risk. Methods: We searched PubMed, Web of Science, Embase, Medline, CNKI and Chinese Biomedical database, covering all publications (up to May, 2014). Statistical analyses were performed with Stata software (version 12.0, USA) and RevMan 5.1 (Copenhagen, 2008). The calculation of odds ratios (ORs) with 95% confidence intervals (CI) was calculated to assess the strength of the association. Results: A total of 15 case-control studies from 13 literatures including 3928 cases and 6012 controls described Asp312Asn genotypes and EC risk. A significant association between XPD Asp312Asn polymorphism and EC risk was found when all the eligible studies were pooled into this meta-analysis. It’s also the same result in subgroup analysis of smokers in dominant model (OR=1.63, 95% CI: 1.06-2.50, emP/em=0.03). However, in the stratified analysis by ethnicity and source of population controls, no association between them was discovered. Conclusion: The XPD Asp312Asn polymorphism was proved to contribute to the risk of EC in this meta-analysis. Data showed that tobacco consumption may increase the susceptibility of EC.
机译:背景:尽管据报道色素干性皮肤病D组(XPD)与食道癌(EC)风险有关,但结果仍然不一致。这项荟萃分析的目的是更精确地估计XPD Asp312Asn多态性与EC风险之间的关系。方法:我们搜索了PubMed,Web of Science,Embase,Medline,CNKI和中国生物医学数据库,涵盖了所有出版物(截至2014年5月)。使用Stata软件(美国12.0版)和RevMan 5.1(哥本哈根,2008年)进行统计分析。计算具有95%置信区间(CI)的优势比(OR),以评估关联强度。结果:来自13篇文献的15项病例对照研究,包括3928例病例和6012例对照,描述了Asp312Asn基因型和EC风险。当所有符合条件的研究纳入该荟萃分析时,发现XPD Asp312Asn多态性与EC风险之间存在显着关联。在主导模型中的吸烟者亚组分析中,结果也相同(OR = 1.63,95%CI:1.06-2.50, P = 0.03)。但是,在按种族和人口控制来源进行的分层分析中,没有发现它们之间的关联。结论:XPD Asp312Asn基因多态性被证明在本荟萃分析中有导致EC的风险。数据显示,烟草消费可能会增加EC的易感性。

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