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Neuropeptide Y Gene Promoter -399T/C Polymorphism Increases Risk of Ischemic Stroke

机译:神经肽Y基因启动子-399T / C多态性增加了缺血性卒中的风险

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摘要

Background: Several genetic factors underlying ischemic stroke have been identified. Variants of Neuropeptide Y (NPY), whose product plays diverse roles in modulating physiological functions, have been associated with an increased risk of ischemic stroke in South Korean individuals. Aims: We explored the association between a polymorphism in the NPY gene promoter at position -399 and the risk of ischemic stroke in Han Chinese. Study Design: Case-control study.Methods: The polymorphism -399T/C in the promoter of NPY was analysed in 500 patients with ischemic stroke and 500 healthy individuals by amplification and sequencing of this region. Non-conditional logistic regression was used to analyse association between genotypes and the risk of ischemic stroke. Results: Genotype and allele frequencies differed significantly between the ischemic stroke and control groups (P0.05). Conclusion: The -399T/C polymorphism of the NPY gene is associated with ischemic stroke in Han Chinese individuals, and the CC genotype may be a risk factor for ischemic stroke.
机译:背景:已识别出缺血性卒中的几个遗传因素。神经肽Y(NPY)的变异,其产品在调节生理功能方面发挥不同的作用,与韩国人的缺血性卒中的风险增加有关。目的:我们探讨了NPE基因启动子在-399位的多态性与汉族缺血性卒中风险的关系。研究设计:案例控制研究。方法:在500例缺血性卒中患者中分析了NPY启动子的多态性-399t / c,通过该地区的扩增和测序分析了500例缺血性卒中和500名健康个体的患者。非条件性逻辑回归用于分析基因型之间的关联和缺血性卒中的风险。结果:基因型和等位基因频率在缺血性卒中和对照组之间有显着不同(P0.05)。结论:NPY基因的-399t / c多态性与汉族人群中缺血性卒中有关,CC基因型可能是缺血性卒中的危险因素。

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