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Variants of the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) gene and risk of ischemic stroke in Han Chinese of eastern China

机译:中国东部汉族人花生四烯酸5-脂氧合酶激活蛋白(ALOX5AP)基因的变异和缺血性中风的风险

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摘要

Variants of the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) gene have been suggested to play an important role in the pathogenesis of atherosclerosis and ischemic stroke. This study was aimed to explore the association of ALOX5AP variants with ischemic stroke risk in Han Chinese of eastern China. A total of 690 ischemic stroke cases and 767 controls were recruited. The subjects were further subtyped according to the Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria. On the basis of that, two polymorphisms of the ALOX5AP gene (rs10507391 and rs12429692) were determined by TaqMan genotyping assay. In addition, plasma leukotriene B4 (LTB4) levels were analyzed in these subjects. There was no evidence of association between the two variants of ALOX5AP and the risk of ischemic stroke or its TOAST-subtypes. Haplotype analysis and stratification analysis according to sex, age, body mass index, hypertension, and diabetes also showed negative association. Analysis of LTB4 levels in a subset of cases and controls revealed that LTB4 levels were significantly higher in ischemic stroke cases than in the controls (70.06±14.75 ng/L vs 57.34±10.93 ng/L; P = 0.000) and carriers of the T allele of the rs10507391 variant were associated with higher plasma LTB4 levels (P = 0.000). The present study suggests there is no association of the two polymorphisms in the ALOX5AP gene with ischemic stroke risk in Han Chinese of eastern China.
机译:有人提出花生四烯酸5-脂氧合酶激活蛋白(ALOX5AP)基因的变体在动脉粥样硬化和缺血性中风的发病机理中起重要作用。这项研究旨在探讨中国东部汉族人群ALOX5AP变异与缺血性卒中风险的关系。总共招募了690名缺血性中风病例和767名对照。根据在急性中风治疗(TOAST)标准中的组织10172试验进一步对受试者进行亚型分析。在此基础上,通过TaqMan基因分型分析确定了ALOX5AP基因的两个多态性(rs10507391和rs12429692)。此外,在这些受试者中分析了血浆白三烯B4(LTB4)水平。没有证据表明ALOX5AP的两种变异与缺血性中风或其TOAST亚型的风险相关。根据性别,年龄,体重指数,高血压和糖尿病进行的单倍型分析和分层分析也显示负相关。对一部分病例和对照中LTB4水平的分析表明,缺血性中风病例中LTB4水平显着高于对照(70.06±14.75 ng / L vs 57.34±10.93 ng / L; P = 0.000)和T携带者rs10507391变体的等位基因与更高的血浆LTB4水平相关(P = 0.000)。本研究表明,在中国东部的汉族人群中,ALOX5AP基因的两个多态性与缺血性卒中风险没有关联。

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