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中国人群中ALOX5AP基因rs10507391/SG13S114 A>T多态性与脑梗死的关联:一项荟萃分析研究

Association of ALOX5AP rs10507391/SG13S114 A>T polymorphism with cerebral infarction in the Chinese population: a meta-analysis study.

作者信息

Ke Xianjin, Wu Xian, Guo Hongming, Li Qian

机构信息

a Department of Neurology , The Affiliated Hospital of Jiangsu University , 438 Jiefang Road, Zhenjiang , Jiangsu , China.

出版信息

Int J Neurosci. 2015;125(10):726-32. doi: 10.3109/00207454.2014.967769. Epub 2014 Oct 22.

Abstract

Various studies have investigated that the single nucleotide polymorphisms (SNPs) rs10507391/SG13S114 A>T polymorphism could increase the risk of cerebral infarction, however these results still remain controversial. Therefore we conducted a meta-analysis to estimate the association of the 5-lipoxygenase-activating protein gene (ALOX5AP) rs10507391/SG13S114 A > T polymorphism with the incidence of cerebral infarction in the Chinese population. Our researchers searched PubMed, Embase, Web of Science databases, China Biological Medicine Database (CBMD), Wanfang Chinese database, and the Chinese National Knowledge Infrastructure (CNKI) database. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were extracted and pooled to assess the strength of the association between the ALOX5AP rs10507391/SG13S114 A>T polymorphism and incidence of cerebral infarction. A total of 12 eligible studies including 6,844 cases and 7,850 controls based on the search criteria were involved in this meta-analysis. The distributions of genotypes in the cases and controls were all in agreement with Hardy-Weinberg equilibrium. We observed that the ALOX5AP rs10507391/SG13S114 A>T polymorphism carried with T allele contrast model, the homozygote codominant model, the heterozygote codominant model, the dominant model and the recessive model (all the models p > 0.05) had no risk of cerebral infarction when all studies were pooled into the meta-analysis. The results of the meta-analysis indicate that ALOX5AP rs10507391/SG13S114 A>T polymorphism is not associated with the risk of cerebral infarction in the Chinese population.

摘要

多项研究调查了单核苷酸多态性(SNP)rs10507391/SG13S114 A>T多态性可能会增加脑梗死风险,但这些结果仍存在争议。因此,我们进行了一项荟萃分析,以评估5-脂氧合酶激活蛋白基因(ALOX5AP)rs10507391/SG13S114 A>T多态性与中国人群脑梗死发病率之间的关联。我们的研究人员检索了PubMed、Embase、科学网数据库、中国生物医学数据库(CBMD)、万方中文数据库和中国知网(CNKI)数据库。提取并汇总了具有95%置信区间(CI)的粗比值比(OR),以评估ALOX5AP rs10507391/SG13S114 A>T多态性与脑梗死发病率之间关联的强度。基于检索标准,共有12项符合条件的研究纳入本次荟萃分析,包括6844例病例和7850例对照。病例组和对照组的基因型分布均符合哈迪-温伯格平衡。我们观察到,在将所有研究纳入荟萃分析时,携带T等位基因对比模型、纯合子共显性模型、杂合子共显性模型、显性模型和隐性模型的ALOX5AP rs10507391/SG13S114 A>T多态性(所有模型p>0.05)均无脑梗死风险。荟萃分析结果表明,ALOX5AP rs10507391/SG13S114 A>T多态性与中国人群脑梗死风险无关。

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