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Four Apolipoprotein B gene polymorphisms and the risk for coronary artery disease: a meta-analysis of 47 studies

机译:四种载脂蛋白B基因多态性与冠心病风险:对47项研究的荟萃分析

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摘要

Apolipoprotein B plays a central role in lipoprotein metabolism. Many studies have evaluated the association between Apolipoprotein B gene polymorphisms (XbaI, EcoRI, SpIns/Del, MspI) and the risk for coronary artery disease and myocardial infarction. However, the results remain inconsistent, particularly among different populations. To more precisely determine the association between Apolipoprotein B gene polymorphisms and coronary artery disease/myocardial infarction risk, we performed a meta-analysis via a comprehensive search of electronic databases (up to February 1st, 2015), odds ratios (OR) and 95 % confidence intervals were calculated using a fixed or random effect model. A total of 47 studies, with 9411 coronary artery disease/myocardial infarction cases and 9082 controls, were included in this meta-analysis. The combined results revealed significant associations between an increased risk of coronary artery disease/myocardial infarction and EcoRI (AA vs GG: OR 1.511, 95 % confidence interval (CI) 1.098, 2.078) and SpIns/Del (DD vs II: OR 1.331, 95 % CI 1.064, 1.665) alleles in the general population. In a subgroup analysis stratified by ethnicity, the T allele of the XbaI variant was associated with a decreased risk in Caucasians, whereas it was associated with an increased risk among the East Asian population. No significant correlation was detected between the A allele of the MspI variant and the coronary artery disease/myocardial infarction risk in either the general population or any ethnic subgroup. The results of our study suggest that Apolipoprotein B gene polymorphisms may affect the coronary artery disease/myocardial infarction susceptibility and these effects may display notable discrepancies among different populations.
机译:载脂蛋白B在脂蛋白代谢中起核心作用。许多研究评估了载脂蛋白B基因多态性(XbaI,EcoRI,SpIns / Del,MspI)与冠状动脉疾病和心肌梗塞风险的关系。但是,结果仍然不一致,尤其是在不同人群之间。为了更准确地确定载脂蛋白B基因多态性与冠状动脉疾病/心肌梗塞风险之间的关联,我们通过全面搜索电子数据库(截至2015年2月1日),优势比(OR)和95%进行了荟萃分析使用固定或随机效应模型计算置信区间。本荟萃分析共纳入47项研究,其中包括9411例冠状动脉疾病/心肌梗塞病例和9082例对照。合并结果显示,冠心病/心肌梗塞的风险增加与EcoRI(AA vs GG:OR 1.511,95%置信区间(CI)1.098,2.078)和SpIns / Del(DD vs II:OR 1.331,普通人群中95%CI 1.064,1.665)等位基因。在按种族分层的亚组分析中,XbaI变异的T等位基因与高加索人的风险降低有关,而与东亚人群的风险增加有关。在普通人群或任何种族亚人群中,在MspI变体的A等位基因与冠状动脉疾病/心肌梗塞风险之间均未发现显着相关性。我们的研究结果表明载脂蛋白B基因多态性可能会影响冠状动脉疾病/心肌梗塞的易感性,并且这些影响可能在不同人群之间显示出显着差异。

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