Wang Jun, Guo Xufeng, Yu Shijie, Zhang Jixiang, Song Jia, Ji Mengyao, Cao Zhuo, Wang Jing, Liu Ya, Dong Weiguo
Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, 430060, Hubei, China.
Mol Biol Rep. 2014;41(4):2679-85. doi: 10.1007/s11033-014-3127-4. Epub 2014 Jan 22.
The C3435T polymorphism of the multidrug resistance gene (MDR1) has been implicated in inflammatory bowel disease (IBD) risk, but the reported results are inconsistent. Here we performed a meta-analysis to evaluate the association between C3435T polymorphism and the risk of IBD using all case-control studies published before February 2013 according to PubMed and Web of Science. A total of 13 case-control studies, including 6,757 cases and 4,295 controls, were included. Pooled odds ratio (OR) with 95 % confidence interval (CI) was calculated using fixed- or random-effects model. Overall, no evidence has indicated that the C3435T polymorphism was associated with the susceptibility to IBD (dominant model: OR = 1.05, 95 % CI: 0.96-1.16; CT vs. CC: OR = 1.06, 95 % CI: 0.95-1.17; TT vs. CC: OR = 1.04, 95 % CI: 0.92-1.17; recessive model: OR = 0.99, 95 % CI: 0.90-1.09). Besides, stratified analysis by clinical type also indicated that no significant association between MDR1 C3435T and the risk of Crohn's disease and ulcerative colitis was observed. This meta-analysis indicated that the C3435T polymorphism of MDR1 may not confer susceptibility to IBD.
多药耐药基因(MDR1)的C3435T多态性与炎症性肠病(IBD)风险相关,但报道结果并不一致。在此,我们进行了一项荟萃分析,根据PubMed和Web of Science检索2013年2月之前发表的所有病例对照研究,以评估MDR1基因C3435T多态性与IBD风险之间的关联。共纳入13项病例对照研究,包括6757例病例和4295例对照。采用固定效应或随机效应模型计算合并比值比(OR)及95%可信区间(CI)。总体而言,尚无证据表明C3435T多态性与IBD易感性相关(显性模型:OR = 1.05,95%CI:0.96 - 1.16;CT vs. CC:OR = 1.06,95%CI:0.95 - 1.17;TT vs. CC:OR = 1.04,95%CI:0.92 - 1.17;隐性模型:OR = 0.99,95%CI:0.90 - 1.09)。此外,按临床类型进行的分层分析也表明,未观察到MDR1基因C3435T与克罗恩病及溃疡性结肠炎风险之间存在显著关联。该荟萃分析表明,MDR1基因的C3435T多态性可能不会使个体易患IBD。