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Significant association between the endothelial lipase gene 584C/T polymorphism and coronary artery disease risk

机译:内皮脂肪酶基因584C / T多态性和冠状动脉疾病风险之间的显着关联

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摘要

Several studies have investigated a potential association between the endothelial lipase gene (LIPG) 584C/T polymorphism and susceptibility to coronary artery disease (CAD), but a uniform conclusion is yet to be reached. To better evaluate the true relationship between the LIPG 584C/T polymorphism and the risk of CAD, a meta-analysis of 14 case–control studies with 9731 subjects was performed. Relevant articles published through August 2020 were searched in the CNKI, PubMed, Embase and Web of Science databases. Thirteen articles, including 14 eligible case–control studies with 4025 cases and 5706 controls, were enrolled in the present meta-analysis. The Newcastle–Ottawa Scale (NOS) scores of the case–control studies ranged from 6 to 8. The pooled results indicated that there is a significant association between the LIPG 584C/T polymorphism and CAD in the homozygote comparison model and the allelic comparison model. Subgroup analyses revealed that the LIPG 584C/T mutation significantly decreased the risk of CAD in the subgroups of African, CAD, hospital-based (HB), and polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) populations in some genetic models. No publication bias was found in our meta-analysis, which certifies the robustness of the current meta-analysis. Trial sequential analysis (TSA) also confirmed the stability of our results. The results of our meta-analysis indicate that the LIPG 584C/T polymorphism plays a protective role in the incidence of CAD. More high-quality case–control studies on various ethnicities are needed to confirm our results.
机译:几项研究已经研究了内皮脂肪酶基因(LIPG)584C / T多态性和对冠状动脉疾病(CAD)的多态性和易感性之间的潜在关联,但尚未结束均匀的结论。为了更好地评估LIPG 584C / T多态性与CAD风险之间的真实关系,进行了具有9731个受试者的14项病例对照研究的META分析。 2020年8月发布的相关文章在CNKI,PubMed,Embase和Sciencease和Web中搜索。在目前的Meta分析中注册了第三篇文章,其中包括具有4025例和5706个对照的合格患者对照研究。核心控制研究的纽卡斯尔 - 渥太华规模(NOS)分数范围为6至8。汇总结果表明,Homozygote比较模型中Lipg 584c / t多态性和CAD之间存在显着关联和等位基因比较模型。亚组分析显示,在一些遗传模型中,Lipg 584c / t突变显着降低了非洲,CAD,基于医院(HB)和聚合酶链反应限制片段长度多态性(PCR-RFLP)群体中的CAD的风险。我们的META分析中没有发现出版物偏见,该分析证明了当前元分析的稳健性。试验顺序分析(TSA)也证实了我们的结果稳定性。我们的Meta分析结果表明LiPG 584C / T多态性在CAD的发生率中起着保护性作用。需要对各种种族进行更高质量的案例控制研究来确认我们的结果。

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