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Effect of the polymorphism of tumor necrosis factor-alpha-308 G/A gene promoter on the susceptibility to ulcerative colitis: a meta-analysis.

机译:肿瘤坏死因子-α-308G / A基因启动子多态性对溃疡性结肠炎易感性的影响:一项荟萃分析。

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摘要

BACKGROUND: Ulcerative colitis (UC) is a complex polygenic disease in which gene-environment interactions are important. Some studies have reported that proinflammatory polymorphisms in tumor necrosis factor-alpha-308 (TNF-alpha-308) gene promoter (substitution G-->A, designated as TNF1 and TNF2) is associated with increased UC risk. However, the results of individual studies have been inconsistent. METHODS: To investigate the inconsistent findings in studies of the association of the polymorphism of TNF-alpha-308 gene promoter with susceptibility to UC, a systematic review of the published data was undertaken and a meta-analysis was performed. The MEDLINE database was searched for case-control studies published in English language journals from 1966 to November 2007. Data were extracted using standardized forms and odds ratios (OR) with 95% confidence intervals (CI) were calculated. RESULTS: 15 eligible studies, 7 of Europeans, 2 of Americans, and 6 of Asians including 4 East Asians, were included in the meta-analysis. An association between UC and TNF2 allele was not found in the overall population (OR 1.28, 95% CI 0.84-1.96, p = 0.25). However, stratification by ethnicity indicated that there was significant association between TNF2 allele and UC in East Asians (OR 2.27, 95% CI 1.08-4.77, p = 0.03). Conversely, there was no association between TNF2 allele and UC patients from the European (OR 0.85, 95% CI 0.42-1.71, p = 0.65) and Asian samples (OR 1.64, 95% CI 0.98-2.74, p = 0.06). The OR for the TNF2/2+TNF2/1 genotype versus TNF1/1 genotype in samples overall and in each ethnic group showed a similar trend to those for the TNF2 allele. CONCLUSION: In East Asians, the TNF2 allele confers a significant risk for developing UC. There is no association between the polymorphism of TNF-alpha-308 gene promoter and UC in Europeans.
机译:背景:溃疡性结肠炎(UC)是一种复杂的多基因疾病,其中基因与环境的相互作用非常重要。一些研究报告说,肿瘤坏死因子-α-308(TNF-α-308)基因启动子中的促炎性多态性(取代G-> A,分别命名为TNF1和TNF2)与UC风险增加有关。但是,个别研究的结果不一致。方法:为了调查在TNF-alpha-308基因启动子多态性与对UC的易感性研究中不一致的发现,对发表的数据进行了系统的综述,并进行了荟萃分析。检索MEDLINE数据库中从1966年至2007年11月在英语期刊上发表的病例对照研究。使用标准化形式提取数据,并计算具有95%置信区间(CI)的比值比(OR)。结果:荟萃分析纳入了15项合格研究,其中7项是欧洲人,2项是美国人,6项是亚洲人,其中包括4名东亚人。在总人群中未发现UC和TNF2等位基因之间的关联(OR 1.28,95%CI 0.84-1.96,p = 0.25)。但是,按种族分层显示,东亚地区TNF2等位基因与UC之间存在显着关联(OR 2.27,95%CI 1.08-4.77,p = 0.03)。相反,来自欧洲(OR 0.85,95%CI 0.42-1.71,p = 0.65)和亚洲样本(OR 1.64,95%CI 0.98-2.74,p = 0.06)的TNF2等位基因与UC患者之间没有关联。总体样本和每个种族样本中TNF2 / 2 + TNF2 / 1基因型与TNF1 / 1基因型的OR趋势与TNF2等位基因相似。结论:在东亚人中,TNF2等位基因赋予罹患UC的重大风险。在欧洲人中,TNF-α-308基因启动子的多态性与UC之间没有关联。

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