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Associations of platelet-activating factor acetylhydrolase gene polymorphisms with risk of ischemic stroke

机译:血小板活化因子乙酰水解酶基因多态性与缺血性中风风险的关系

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摘要

Platelet-activating factor acetylhydrolase (PAF-AH) has an important function in the pathogenesis of ischemic stroke. The aim of the present study was to investigate the correlation between the variation of polymorphisms (R92H and V279F) in PAF-AH and ischemic stroke. A total of 375 patients with ischemic stroke and 370 healthy controls were recruited into the study. Polymorphisms of V279F and R92H in PAF-AH were detected by polymerase chain reaction and DNA direct sequencing method. No significant association was observed between V279F and ischemic stroke. However, the RH+HH genotype, RH genotype and H allele of R92H were significantly associated with an increased risk of ischemic stroke (P=0.02, P=0.03 and P=0.02, respectively), In addition, these correlations remained following adjustment for confounding risk factors of stroke. Furthermore, subgroup analysis showed that a significant association with R92H was identified in the large-artery atherosclerotic stroke subgroup. These findings indicated that variation of R92H in the PAF-AH gene may contribute to ischemic stroke susceptibility in the population studied.
机译:血小板活化因子乙酰水解酶(PAF-AH)在缺血性中风的发病机制中具有重要作用。本研究的目的是研究PAF-AH中多态性(R92H和V279F)变异与缺血性中风之间的相关性。研究共招募了375名缺血性中风患者和370名健康对照。通过聚合酶链反应和DNA直接测序法检测PAF-AH中V279F和R92H的多态性。在V279F和缺血性中风之间未观察到显着关联。然而,R92H的RH + HH基因型,RH基因型和H等位基因与缺血性中风的风险增加显着相关(分别为P = 0.02,P = 0.03和P = 0.02),此外,在调整了混淆中风的危险因素。此外,亚组分析显示,在大动脉粥样硬化性卒中亚组中发现与R92H显着相关。这些发现表明,PAF-AH基因中R92H的变异可能有助于所研究人群的缺血性中风敏感性。

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