Department of Internal Neurology, First Affiliated Hospital, Guangxi University of Chinese Medicine, Nanning, Guangxi, China.
J Neurol Sci. 2013 Jul 15;330(1-2):100-10. doi: 10.1016/j.jns.2013.04.022. Epub 2013 May 16.
Recently, increasing studies have been focused on the association between the p22phox gene C242T polymorphism and ischemic stroke (IS). However, the results were controversial. As far as we know, there is no previous systematic review or meta-analysis concerning this association. Thus, we conducted this meta-analysis to evaluate this association. The strength of association was evaluated by the odds ratio (OR) with the corresponding 95% confidence intervals (CIs). Heterogeneity was assessed by Q-test and the I(2) statistic. Publication bias was tested using funnel plots and Egger's regression test. Cumulative meta-analysis was performed to assess the trend in pooled OR over time. There was no significant association of the p22phox gene C242T polymorphism with IS in the overall analysis and subgroup analysis by ethnicity and subtypes of IS. However, statistical significance was found in the dominant model (OR: 1.57, 95%CI: 1.18-2.09), codominant model (OR: 1.62, 95%CI: 1.20-2.17) and allelic model (OR: 1.44, 95%CI: 1.11-1.87) among the hospital-based studies. The cumulative meta-analysis also suggested no trend of association between this polymorphism and IS from 2007 to 2011 as more data accumulated over time. Our meta-analysis indicated that the p22phox gene C242T polymorphism is unrelated to the risk of IS in the overall analysis and subgroup analysis by ethnicity and subtypes of IS. However, statistical significance was found in the subgroup analysis by source of controls among the hospital-based studies.
最近,越来越多的研究集中在 p22phox 基因 C242T 多态性与缺血性脑卒中(IS)之间的关联上。然而,结果存在争议。据我们所知,以前没有关于这种关联的系统评价或荟萃分析。因此,我们进行了这项荟萃分析来评估这种关联。关联的强度通过比值比(OR)及其相应的 95%置信区间(CI)来评估。异质性通过 Q 检验和 I(2)统计量来评估。使用漏斗图和 Egger 回归检验来测试发表偏倚。累积荟萃分析用于评估随时间变化的汇总 OR 趋势。在总体分析和按种族和 IS 亚型进行的亚组分析中,p22phox 基因 C242T 多态性与 IS 没有显著关联。然而,在基于医院的研究中,在显性模型(OR:1.57,95%CI:1.18-2.09)、共显性模型(OR:1.62,95%CI:1.20-2.17)和等位基因模型(OR:1.44,95%CI:1.11-1.87)中发现了统计学意义。累积荟萃分析还表明,随着时间的推移,随着数据的积累,这种多态性与 IS 之间没有关联的趋势。我们的荟萃分析表明,在总体分析和按种族和 IS 亚型进行的亚组分析中,p22phox 基因 C242T 多态性与 IS 的风险无关。然而,在基于医院的研究中,在对照来源的亚组分析中发现了统计学意义。