Lu XiaoCheng, Tang Linjun, Li Kai, Zheng JinYu, Zhao Penglai, Tao Yi, Li Li-Xin
1] Department of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu, 210029, China [2].
Department of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, Jiangsu, 210029, China.
Sci Rep. 2014 Jan 29;4:3924. doi: 10.1038/srep03924.
Polymorphisms in NKX2-3 gene have been inconsistently associated with Crohn's disease (CD) and ulcerative colitis (UC). To generate large-scale evidence on whether NKX2-3 polymorphisms are associated with CD or UC susceptibility we have conducted a meta-analysis of 17 studies involving 17329 patients and 18029 controls. A significantly increased CD or UC risk was observed in persons carrying a G allele at rs10883365 polymorphism (A/G) compared with those with a A allele. (OR = 1.226, 95%CI: 1.177-1.277 and OR = 1.274, 95%CI: 1.175-1.382 respectively). In the subgroup analysis, a significantly increased CD risk was found in both Europeans and Asians. For rs11190140 polymorphism (C/T) and CD risk, the risk estimate for the allele contrast was OR = 1.201 (1.136-1.269). This meta-analysis provided a robust result that persons with a G or T allele may have a moderately increased risk of CD, and suggested that rs10883365 polymorphism was also a candidate gene polymorphism for UC susceptibility.
NKX2 - 3基因多态性与克罗恩病(CD)和溃疡性结肠炎(UC)的相关性一直存在争议。为了获取关于NKX2 - 3基因多态性是否与CD或UC易感性相关的大规模证据,我们对17项研究进行了荟萃分析,这些研究共纳入17329例患者和18029例对照。与携带A等位基因的人相比,携带rs10883365多态性(A/G)G等位基因的人患CD或UC的风险显著增加。(OR = 1.226,95%CI:1.177 - 1.277;OR = 1.274,95%CI:1.175 - 1.382)。在亚组分析中,欧洲人和亚洲人中患CD的风险均显著增加。对于rs11190140多态性(C/T)与CD风险,等位基因对比的风险估计值为OR = 1.201(1.136 - 1.269)。这项荟萃分析提供了有力证据,表明携带G或T等位基因的人患CD的风险可能适度增加,并提示rs10883365多态性也是UC易感性的候选基因多态性。