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Interleukin-18 gene promoter 607A polymorphism but not 137C polymorphism is a protective factor for ischemic stroke in the Chinese population: A meta-analysis

机译:白介素-18基因启动子607A多态性而非137C多态性是中国人群缺血性卒中的保护因素:一项荟萃分析

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摘要

Some epidemiological studies have evaluated the association between interleukin (IL)-18 promoter polymorphisms and the risk of ischemic stroke (IS), but the results were inconsistent. The present meta-analysis was therefore performed to investigate the relationship between IL-18 promoter 137G/C and 607C/A polymorphisms and the risk of IS in the Chinese population. Related studies from PubMed, Embase, Web of Science, CBMdisc and CNKI databases up to November 1, 2014 were systematically searched, also the reference lists of identified articles were manually searched. Information was extracted to calculate for the allelic, genotypic, dominant and recessive models using the pooled odds ratios (ORs) along with 95% confidence intervals (CIs). Evidence of significant association between 607C/A polymorphism and risk of IS was found in four genetic models based on the overall population. However, no significant association between 137G/C polymorphism and risk of IS was found in four genetic models. In summary, the present study suggests that IL-18 gene promoter 607A polymorphism is a protective factor for IS in the Chinese population, while 137C polymorphism has weaker or no protective properties. Still, a larger number of studies with large scale and sufficient original information are required to further confirm our findings.
机译:一些流行病学研究评估了白介素(IL)-18启动子多态性与缺血性中风(IS)风险之间的关联,但结果不一致。因此,本荟萃分析旨在研究IL-18启动子137G / C和607C / A多态性与中国人群IS风险之间的关系。系统搜索了截至2014年11月1日来自PubMed,Embase,Web of Science,CBMdisc和CNKI数据库的相关研究,还手动搜索了已鉴定文章的参考清单。使用汇总的比值比(OR)以及95%的置信区间(CI)提取信息以计算等位基因,基因型,显性和隐性模型。在基于总种群的四个遗传模型中,发现607C / A多态性与IS风险之间存在显着关联的证据。但是,在四个遗传模型中未发现137G / C多态性与IS风险之间有显着关联。总而言之,本研究表明IL-18基因启动子607A多态性是中国人群IS的保护因子,而137C多态性则弱或无保护性。尽管如此,仍需要大量的大规模研究和足够的原始信息来进一步证实我们的发现。

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