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首页> 外文期刊>Blood coagulation & fibrinolysis: an international journal in haemostasis and thrombosis >Association of renin-angiotensin system genes polymorphisms and risk of premature ST elevation myocardial infarction in young Mexican population
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Association of renin-angiotensin system genes polymorphisms and risk of premature ST elevation myocardial infarction in young Mexican population

机译:肾素 - 血管紧张素系统基因多态性的关联与户外墨西哥人群的早产儿腹膜心肌梗死的风险

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摘要

The renin-angiotensin system plays an important role in the regulation of blood pressure and the development of coronary artery disease. The aim was to examine the association of the insertion deletion in the angiotensin-converting enzyme gene, M235T and T174M polymorphisms in the angiotensinogen gene with ST elevation acute myocardial infarction (STEAMI) in young Mexican population. We analyzed 242 unrelated patients with STEAMI 45 or less years of age, admitted to a cardiovascular intense care unit, and 242 individuals without STEAMI matched by age and sex, recruited from January 2006 and June 2013. The polymorphisms insertion deletion, M235T and T174M were determined in all participants by a polymerase chain-reaction-restriction fragment length polymorphism assay. There was a significant difference in the insertion deletion genotype distribution between two groups (P=0.03) and a higher percentage of the T allele M235T polymorphism in the group of STEAMI patients (P=0.02). The T174M polymorphism was not associated (P=0.08). The insertion deletion and M235T polymorphisms, smoking, hypertension, familial history of cardiovascular disease and dyslipidemia were independent risk factors for STEAMI. Our results identified that the D allele from the insertion deletion and M235T but not T174M polymorphisms represent an independent risk factor for STEAMI in young Mexican population.
机译:肾素 - 血管紧张素系统在调节血压和冠状动脉疾病的发展中起着重要作用。目的是在血管紧张素素基因中检查血管紧张素素转换酶基因,M235T和T174M多态性中的插入缺失与年轻墨西哥人群的ST急性心肌梗死(Steami)中的血管紧张素原基因。我们分析了242名无关患者的Steami 45或多年来的患者,进入心血管强烈的护理单位,242名没有Steami的人,从2006年1月和2013年6月招募了年龄和性别。多态性插入删除,M235T和T174M通过聚合酶链反应限制片段长度多态性测定在所有参与者中确定。两组(P = 0.03)之间的插入缺失基因型分布和蒸汽患者组中的T等位基因M235T多态性较高的差异有显着差异(P = 0.02)。 T174M多态性无相关(P = 0.08)。插入缺失和M235T多态性,吸烟,高血压,家族性历史的心血管疾病和血脂血症是Steami的独立危险因素。我们的结果发现,来自插入缺失和M235T但不是T174M多态性的D等位基因代表了年轻墨西哥人群中Steami的独立危险因素。

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