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Association of CYP11B2 gene polymorphism with ischemic stroke in the north Chinese Han population

机译:CYP11B2基因多态性与中国北方汉族人群缺血性卒中的相关性

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Background: Genetic variations of renin-angiotensin-aldosterone system play an important role in the pathogenesis of hypertension and stroke. Aim: To investigate the -344C/T and intron 2 conversion polymorphisms of aldosterone synthase gene (CYP11B2) for an association with stroke and hypertension in the North Chinese Han population. Materials and Methods: This case-control study included 332 patients and 250 controls. Genotypes of -344C/T polymorphism was determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and the intron 2 conversion polymorphism was genotyped using two separated PCRs. Results: There were significant differences in genotype frequencies of -344C/T polymorphism between stroke patients and controls (P = 0.002). An association was found between TT genotype and ischemic stroke [odds ratio = 1.572, 95%CI (1.095-2.258), P = 0.014]. However, there was no significant association of intron 2 polymorphism with stroke. Furthermore, when the ischemic stroke patients were classified according to Trial of Org 10172 in Acute Stroke Treatment classification, TT genotype was found to be associated with large artery atherosclerosis [odds ratio = 1.747, 95%CI (1.182-2.584), P = 0.005] and small vessel disease [odds ratio = 1.781, 95%CI (1.134-2.796), P = 0.012]. The intron 2 polymorphism failed to show relationship with any specific stroke subtype. Conclusions: Our findings suggest a significant association of CYP11B2 (-344C/T) polymorphism with stroke but intron 2 polymorphism is not associated with increased stroke susceptibility.
机译:背景:肾素-血管紧张素-醛固酮系统的遗传变异在高血压和中风的发病机理中起重要作用。目的:研究醛固酮合酶基因(CYP11B2)的-344C / T和内含子2转换多态性与华北汉族人群中风和高血压的关系。材料和方法:本病例对照研究包括332名患者和250名对照。通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)确定-344C / T多态性的基因型,并使用两个分离的PCR对内含子2转化多态性进行基因分型。结果:中风患者与对照组之间-344C / T基因多态性的基因型频率存在显着差异(P = 0.002)。发现TT基因型与缺血性卒中之间存在关联[比值= 1.572,95%CI(1.095-2.258),P = 0.014]。但是,内含子2多态性与中风没有显着关联。此外,根据缺血性卒中患者在急性卒中治疗分类中按照Org 10172试验进行分类时,发现TT基因型与大动脉粥样硬化相关[比值比= 1.747、95%CI(1.182-2.584),P = 0.005 ]和小血管疾病[赔率= 1.781,95%CI(1.134-2.796),P = 0.012]。内含子2的多态性未能显示与任何特定的中风亚型的关系。结论:我们的发现提示CYP11B2(-344C / T)多态性与中风显着相关,但内含子2多态性与中风易感性增加无关。

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