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CARD8基因rs2043211多态性与炎症性肠病的关联:一项荟萃分析

Association between CARD8 rs2043211 polymorphism and inflammatory bowel disease: a meta-analysis.

作者信息

Liu Juan, Liu Yan-Yan, Liu Jie, Li Bao-Zhu, Cen Han, Xu Wang-Dong, Leng Rui-Xue, Pan Hai-Feng, Ye Dong-Qing

机构信息

Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University , Hefei, Anhui , PR China and.

出版信息

Immunol Invest. 2015;44(3):253-64. doi: 10.3109/08820139.2014.988721. Epub 2015 Jan 7.

DOI:10.3109/08820139.2014.988721
PMID:25564880
Abstract

OBJECTIVE

The aim of this study was to determine whether caspase recruitment domain-containing protein 8 (CARD8) rs2043211 polymorphism was associated with susceptibility to inflammatory bowel disease (IBD).

METHODS

Relevant studies were searched using PubMed and Embase up to February 2014. A meta-analysis was conducted on the association between rs2043211 polymorphism and IBD using: (1) allele contrast, (2) the dominant model, (3) the recessive model, and (4) homozygote contrast. The pooled estimated of risk was obtained by random-effects model or fixed-effects model. Publication bias was assessed by Egger's test.

RESULTS

Eight relevant articles with a total of 10 534 IBD patients [6785 Crohn's disease (CD), 3713 ulcerative colitis (UC) and 36 indeterminate colitis (IC)] and 6755 healthy controls were included in the meta-analysis, which consisted of 12 studies, 12 for CD, 10 for UC, 2 for IC. There was no significant association between rs2043211 polymorphism and IBD, CD, and IC in overall population. However, stratified meta-analysis by ethnicity showed significant association between rs2043211 polymorphism and CD in the European population under the dominant model [odds ratio (OR) = 1.210, 95% confidence interval (CI) = 1.013-1.445, p = 0.036] and homozygote contrast (OR = 1.212, 95% CI = 1.005-1.461, p = 0.044).

CONCLUSIONS

Our meta-analysis results indicated significant association between rs2043211 polymorphism and the susceptibility to CD under the dominant model and homozygote contrast in the European population.

摘要

目的

本研究旨在确定含半胱天冬酶招募结构域蛋白8(CARD8)rs2043211多态性是否与炎症性肠病(IBD)易感性相关。

方法

截至2014年2月,使用PubMed和Embase检索相关研究。采用以下方法对rs2043211多态性与IBD之间的关联进行荟萃分析:(1)等位基因对比;(2)显性模型;(3)隐性模型;(4)纯合子对比。通过随机效应模型或固定效应模型获得风险的合并估计值。采用Egger检验评估发表偏倚。

结果

荟萃分析纳入了8篇相关文章,共10534例IBD患者[6785例克罗恩病(CD)、3713例溃疡性结肠炎(UC)和36例未定型结肠炎(IC)]以及6755例健康对照,这些研究包括12项,其中CD相关研究12项、UC相关研究10项、IC相关研究2项。总体人群中,rs2043211多态性与IBD、CD和IC之间无显著关联。然而,按种族进行分层荟萃分析显示,在显性模型下,欧洲人群中rs2043211多态性与CD存在显著关联[比值比(OR)=1.210,95%置信区间(CI)=1.013 - 1.445,p = 0.036],在纯合子对比中也存在显著关联(OR = 1.212,95%CI = 1.005 - 1.461,p = 0.044)。

结论

我们的荟萃分析结果表明,在欧洲人群中,显性模型和纯合子对比下,rs2043211多态性与CD易感性之间存在显著关联。

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