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APC polymorphisms and the risk of colorectal neoplasia: A huge review and meta-analysis

机译:APC基因多态性与结直肠癌的风险:巨大的回顾和荟萃分析

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Adenomatous polyposis coli gene (APC) polymorphisms may influence the risk for colorectal neoplasia. However, results thus far have been inconclusive. We performed a systematic literature search of the Medline, Embase, Cochrane Collaboration, and HuGE databases and reviewed the references of pertinent articles through May 2012. Odds ratios with 95% confidence intervals were used to estimate the association between 3 APC polymorphisms (D1822V, E1317Q, and I1307K) and colorectal neoplasia. In total, 40 studies from 1997 to 2010 were included in this meta-analysis, and individuals with the D1822V variant homozygote VV genotype had a slight decrease in the risk for colorectal neoplasia compared with the wild-type homozygote DD genotype (pooled odds ratio = 0.87, 95% confidence interval: 0.77, 0.99). There was a small association between the APC E1317Q polymorphism and a risk for colorectal neoplasia (variant vs. wild-type: pooled odds ratio = 1.41, 95% confidence interval: 1.14, 1.76), particularly for colorectal adenomas (variant vs. wild-type: odds ratio = 2.89, 95% confidence interval: 1.83, 4.56). Compared with those who carried the wild-type I1307K, Ashkenazi Jews who carried the I1307K variant were at a significantly increased risk for colorectal neoplasia, with a pooled odds ratio of 2.17 (95% confidence interval: 1.64, 2.86). Our study suggests that APC is a candidate gene for colorectal neoplasia susceptibility.
机译:腺瘤性息肉病大肠杆菌基因(APC)多态性可能会影响结直肠癌的风险。但是,迄今为止的结果尚无定论。我们对Medline,Embase,Cochrane Collaboration和HuGE数据库进行了系统的文献检索,并审查了截至2012年5月的相关文章的参考文献。使用具有95%置信区间的几率来估计3种APC多态性之间的关联(D1822V,E1317Q和I1307K)和结直肠肿瘤。这项荟萃分析共纳入1997年至2010年的40项研究,与野生型纯合子DD基因型相比,具有D1822V变异纯合子VV基因型的个体患结直肠瘤的风险略有降低(合并优势比= 0.87,95%置信区间:0.77,0.99)。 APC E1317Q多态性与结直肠瘤形成的风险之间存在很小的关联(变异vs.野生型:合并优势比= 1.41,95%置信区间:1.14,1.76),特别是结直肠腺瘤(变异vs.野生型)。类型:比值比= 2.89,95%置信区间:1.83,4.56)。与携带野生型I1307K的人相比,携带I1307K变体的Ashkenazi犹太人患结直肠瘤的风险显着增加,合并比值比为2.17(95%置信区间:1.64、2.86)。我们的研究表明,APC是结肠直肠肿瘤易感性的候选基因。

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