Song Di, Cheng Daobin
Department of Neurology, The First Affiliated Hospital of Guangxi Medical University , Nanning, China .
Genet Test Mol Biomarkers. 2017 Jan;21(1):10-16. doi: 10.1089/gtmb.2015.0265. Epub 2016 Nov 3.
Two well-characterized polymorphisms in the tumor necrosis factor (TNF) gene, TNFα-308G/A and TNFα-238G/A, are thought to play important roles in the etiology and pathogenesis of ischemic stroke. Due to ethnic diversity, studies of the associations between these polymorphisms and ischemic stroke are inconclusive. Thus, we conducted a meta-analysis to derive more precise estimates of these associations in East Asians and non-East Asians.
We searched relevant publications in the PubMed, Embase, and Medline databases. A total of 18 studies with 8075 patients and 8217 controls were included. The odds ratios (OR) and 95% confidence intervals (CIs) were evaluated to identify associations.
Analyses of the full dataset failed to identify any significant association between ischemic stroke and the TNFα-308G/A (A vs. G: OR = 0.86, 95% CI: 0.72-1.02, p = 0.08) or TNFα-238G/A (A vs. G: OR = 0.94, 95% CI: 0.67-1.32, p = 0.72) polymorphism. In subgroup analysis by ethnicity, TNFα-308G/A was found to be a protective factor (A vs. G: OR = 0.69, 95% CI: 0.56-0.85, p = 0.01) against ischemic stroke in the East Asians. No significant association was detected between ischemic stroke risk and TNFα-238G/A in the East Asians (A vs. G: OR = 0.82, 95% CI: 0.57-1.16, p = 0.26) or non-East Asians (A vs. G: OR = 1.61, 95% CI: 0.90-2.88, p = 0.11).
The results of this meta-analysis suggest that there is no significant relationship between ischemic stroke and TNFα-308G/A or TNFα-238G/A. However, according to subgroup analysis of East Asians, TNFα-308G/A is a protective factor against ischemic stroke.
肿瘤坏死因子(TNF)基因中的两种特征明确的多态性,即TNFα - 308G/A和TNFα - 238G/A,被认为在缺血性中风的病因和发病机制中起重要作用。由于种族差异,关于这些多态性与缺血性中风之间关联的研究尚无定论。因此,我们进行了一项荟萃分析,以更精确地评估东亚人和非东亚人中这些关联。
我们在PubMed、Embase和Medline数据库中搜索相关出版物。共纳入18项研究,涉及8075例患者和8217例对照。评估比值比(OR)和95%置信区间(CI)以确定关联。
对整个数据集的分析未发现缺血性中风与TNFα - 308G/A(A vs. G:OR = 0.86,95% CI:0.72 - 1.02,p = 0.08)或TNFα - 238G/A(A vs. G:OR = 0.94,95% CI:0.67 - 1.32,p = 0.72)多态性之间存在任何显著关联。在按种族进行的亚组分析中,发现TNFα - 308G/A是东亚人缺血性中风的保护因素(A vs. G:OR = 0.69,95% CI:0.56 - 0.85,p = 0.01)。在东亚人(A vs. G:OR = 0.82,95% CI:0.57 - 1.16,p = 0.26)或非东亚人(A vs. G:OR = 1.61,95% CI:0.90 - 2.88,p = 0.11)中,未检测到缺血性中风风险与TNFα - 238G/A之间存在显著关联。
这项荟萃分析的结果表明,缺血性中风与TNFα - 308G/A或TNFα - 238G/A之间无显著关系。然而,根据东亚人的亚组分析,TNFα - 308G/A是缺血性中风的保护因素。