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AGT M235T polymorphisms and ischemic stroke risk: A meta-analysis

机译:AGT M235T基因多态性与缺血性中风的风险:一项荟萃分析

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摘要

Recently, the association between AGT M235T polymorphism and ischemic stroke (IS) has attracted widespread attention, and many investigations have been performed. However, the results were inconsistent. Therefore, we performed a meta-analysis to further evaluate the association between M235T and IS. All of the relevant studies were identified from PubMed, EMBASE, Chinese National Knowledge Infrastructure database (CNKI), Chinese Biological Medical Literature database (CBM), Chinese Wanfang and Chongqing VIP database up to January 2013. Statistical analyses were conducted with STATA software version 11.1. Odds ratios with 95% confidence interval were applied to evaluate the strength of the association. We performed the cumulative meta-analysis to assess the tendency of pooled OR over time. Heterogeneity was evaluated by Q-test and the I 2 statistic. The funnel plots and Egger's regression test were used to assess the publication bias. A significant association between AGT M235T polymorphism and IS was found under the dominant model (OR = 1.368, 95% CI = 1.070-1.749), recessive model (OR = 1.66, 95% CI = 1.310-2.103), overdominant model (OR = 1.285, 95% CI = 1.085-1.523), co-dominant model (OR = 1.574, 95% CI = 1.276- 1.942) and allele model (OR = 1.447, 95% CI = 1.207-1.735). Besides the Caucasian and the populationbased controls, significant association could be found in the subgroup analysis of Asian and hospital-based controls. Results from cumulative analysis showed a tendency of significant association of this polymorphism with IS. However, the opposite trend was observed among Caucasians. Results from our meta-analysis indicated that the AGT M235T polymorphism might be a risk factor for IS among Asians, but not for Caucasians. More studies are required to further confirm our findings.
机译:最近,AGT M235T基因多态性与缺血性中风(IS)之间的关联已引起广泛关注,并且已进行了许多研究。但是,结果不一致。因此,我们进行了荟萃分析,以进一步评估M235T和IS之间的关联。截至2013年1月,所有相关研究均来自PubMed,EMBASE,中国国家知识基础设施数据库(CNKI),中国生物医学文献数据库(CBM),中国万方和重庆VIP数据库。使用STATA软件11.1版进行统计分析。 。应用置信区间为95%的几率来评估关联的强度。我们进行了累积荟萃分析,以评估合并OR随时间变化的趋势。通过Q检验和I 2统计评估异质性。漏斗图和Egger回归测试用于评估出版偏倚。在优势模型(OR = 1.368,95%CI = 1.070-1.749),隐性模型(OR = 1.66,95%CI = 1.310-2.103),显性模型(OR = 1.285、95%CI = 1.085-1.523),共显性模型(OR = 1.574,95%CI = 1.276-1.942)和等位基因模型(OR = 1.447,95%CI = 1.207-1.735)。除了高加索人和基于人群的对照外,在亚洲人和医院对照的亚组分析中也可以发现显着的相关性。累积分析的结果表明该多态性与IS显着相关。但是,在高加索人中观察到相反的趋势。我们的荟萃分析结果表明,AGT M235T基因多态性可能是亚洲人患IS的危险因素,但对于白种人却不是。需要更多的研究来进一步证实我们的发现。

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