Laboratory of Disorder Genes and Department of Pharmacology, College of Pharmacy, Chongqing Medical University, 1 Yi Xue Yuan Road, P. O. Box 380, Chongqing 400016, People's Republic of China.
Mol Biol Rep. 2012 Feb;39(2):1575-83. doi: 10.1007/s11033-011-0896-x. Epub 2011 Jun 3.
Tumor necrosis factor-alpha (TNF-α) has been regarded as a candidate gene for Crohn's disease (CD) based on its inflammatory function in immune reaction and the clinical effectiveness of anti-TNF-α therapy. However, studies to date have reported inconsistent findings for the association between TNF-α and CD. The PubMed, EMBASE, and Medline databases were systematically reviewed from all English language publications up to April, 2011. A total of twenty-nine studies concerning the association between CD and the TNF-α promoter polymorphisms of -308G/A, -857C/T and -238G/A were identified, among of them only twenty-three studies match the inclusion criteria (including 3,843 cases and 6,260 controls) and were selected for the statistical test. We found that neither the G allele of -308G/A (OR 1.02, 95% CI 0.87-1.19, P = 0.84), C allele of -857C/T (OR 0.97, 95% CI 0.86-1.09, P = 0.57) and G allele of -238G/A (OR 0.91, 95% CI 0.70-1.18, P = 0.48), and nor their GG (OR 1.05, 95% CI 0.88-1.25, P = 0.59), CC (OR 0.98, 95% CI 0.86-1.12, P = 0.76) and GG (OR 0.92, 95% CI 0.70-1.21, P = 0.55) genotypes were associated with CD susceptibility, respectively. Our meta-analysis demonstrates that three promoter polymorphisms of TNF-α above may not confer susceptibility to CD.
肿瘤坏死因子-α(TNF-α)因其在免疫反应中的炎症功能以及抗 TNF-α 治疗的临床效果,被认为是克罗恩病(CD)的候选基因。然而,迄今为止的研究对于 TNF-α与 CD 之间的关联结果并不一致。我们系统性地检索了 PubMed、EMBASE 和 Medline 数据库,检索截至 2011 年 4 月所有英文语种的出版物。共发现 29 项关于 TNF-α启动子多态性-308G/A、-857C/T 和 -238G/A 与 CD 之间关联的研究,其中仅有 23 项研究符合纳入标准(包括 3843 例病例和 6260 例对照),并进行了统计学检验。我们发现,TNF-α-308G/A 的 G 等位基因(OR 1.02,95%CI 0.87-1.19,P=0.84)、-857C/T 的 C 等位基因(OR 0.97,95%CI 0.86-1.09,P=0.57)和 -238G/A 的 G 等位基因(OR 0.91,95%CI 0.70-1.18,P=0.48),以及它们的 GG(OR 1.05,95%CI 0.88-1.25,P=0.59)、CC(OR 0.98,95%CI 0.86-1.12,P=0.76)和 GG(OR 0.92,95%CI 0.70-1.21,P=0.55)基因型与 CD 易感性均无关。我们的荟萃分析表明,TNF-α 上述三个启动子多态性可能与 CD 易感性无关。