肿瘤坏死因子-α (-238G/A和-308G/A)基因多态性与缺血性脑卒中风险的相关性:一项荟萃分析

IF 3.8 Q1 PERIPHERAL VASCULAR DISEASE
Pulse Pub Date : 2016-04-01 Epub Date: 2016-02-17 DOI:10.1159/000443770
Pradeep Kumar, Shubham Misra, Amit Kumar, Awadh Kishor Pandit, Kamalesh Chakravarty, Kameshwar Prasad
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引用次数: 18

摘要

肿瘤坏死因子-α (TNF-α)是一种促炎的多效细胞因子,可能参与缺血性脑卒中(is)的发生和发展。到目前为止,已经进行了大量的研究来研究TNF-α基因启动子区域-238G/A (rs361525)和-308G/A (rs1800629)多态性与IS易感性之间的关系,但结果仍然相互矛盾。本荟萃分析的目的是提供TNF-α -238G/ a和-308G/ a基因多态性与is易感性之间关系的相对全面的解释。在PubMed、Medline、EMBASE和Google Scholar数据库中检索2015年4月20日前发表的符合条件的候选基因研究。使用以下主要关键词组合:(肿瘤坏死因子-α或TNF-α)和(缺血性中风或脑梗死或IS)和(遗传多态性或单核苷酸多态性或SNP)。固定效应或随机效应模型用于估计合并优势比(or)和95%置信区间(CI)。采用RevMan 5.3软件进行meta分析。对于TNF-α -238G/A基因多态性,7项病例对照研究(共1846例IS患者和1905例对照)显示,在显性模型下,TNF-α -238G/A基因多态性与IS易感性显著相关(AA + GA vs. GG;或者,1.40;95% ci, 1.11-1.76;P值0.004)。对于TNF-α -308G/A基因多态性,16项病例对照研究(共5,651例IS患者和5,792例对照)显示,在显性模型下,TNF-α -308G/A基因多态性与IS易感性存在显著的保护性关联(AA + GA vs. GG;Or为0.78,95% ci为0.63-0.97;P值为0.03)。我们的荟萃分析显示,与亚洲人群相比,TNF-α -238G/A基因多态性更可能与白种人患is的风险相关。然而,与高加索人群相比,TNF-α -308G/A基因多态性在亚洲人群中更可能对is具有保护作用。需要进一步的大型、设计良好的前瞻性流行病学研究来证实这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Association between Tumor Necrosis Factor-α (-238G/A and -308G/A) Gene Polymorphisms and Risk of Ischemic Stroke: A Meta-Analysis.

Association between Tumor Necrosis Factor-α (-238G/A and -308G/A) Gene Polymorphisms and Risk of Ischemic Stroke: A Meta-Analysis.

Association between Tumor Necrosis Factor-α (-238G/A and -308G/A) Gene Polymorphisms and Risk of Ischemic Stroke: A Meta-Analysis.

Association between Tumor Necrosis Factor-α (-238G/A and -308G/A) Gene Polymorphisms and Risk of Ischemic Stroke: A Meta-Analysis.

Tumor necrosis factor-α (TNF-α) is a proinflammatory pleiotropic cytokine which may contribute to the initiation and progression of ischemic stroke (IS). Thus far, numerous studies have been performed to examine the association between -238G/A (rs361525) and -308G/A (rs1800629) polymorphisms in the promoter regions of the TNF-α gene and susceptibility to IS, but results are still conflicting. The aim of this meta-analysis is to provide a relatively comprehensive account of the association between TNF-α -238G/A and -308G/A gene polymorphisms and susceptibility to IS. A literature search for eligible candidate gene studies published before April 20, 2015, was conducted in the PubMed, Medline, EMBASE and Google Scholar databases. The following combinations of main keywords were used: ('Tumor Necrosis Factor-Alpha' or 'TNF-α') and ('ischemic stroke' or 'cerebral infarction' or 'IS') and ('genetic polymorphism' or 'single nucleotide polymorphisms' or 'SNP'). Fixed- or random-effect models were used to estimate the pooled odds ratio (OR) and 95% confidence interval (CI). Meta-analysis was carried out by using RevMan 5.3 software. For TNF-α -238G/A gene polymorphism, 7 case-control studies with a total of 1,846 IS patients and 1,905 controls showed a significant association with susceptibility to IS under a dominant model (AA + GA vs. GG; OR, 1.40; 95% CI, 1.11-1.76; p value 0.004). For TNF-α -308G/A gene polymorphism, 16 case-control studies with a total of 5,651 IS patients and 5,792 controls showed a significant protective association with susceptibility to IS under a dominant model (AA + GA vs. GG; OR, 0.78, 95% CI, 0.63-0.97; p value 0.03). Our meta-analysis shows that TNF-α -238G/A gene polymorphism is more likely to be associated with the risk of IS in Caucasian populations as compared to Asian populations. However, TNF-α -308G/A gene polymorphism is more likely to be protective against IS in Asian populations as compared to Caucasian populations. Further large, well-designed prospective epidemiological studies are needed to confirm these findings.

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