The genetic factor in acute myocardial infarction with hypertension.

S. Aoki, S. Mukae, S. Itoh, R. Sato, K. Nishio, T. Iwata, T. Katagiri
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引用次数: 20

Abstract

This study assessed the contribution of polymorphisms of angiotensin II (AngII) receptors and bradykinin B2 (BK-B2) receptor to hypertension and acute myocardial infarction (AMI) in a Japanese population: 150 subjects with essential hypertension, 150 subjects with AMI with/without hypertension, and 150 healthy, age- and sex-matched controls. Polymorphisms of the AngII type 1 receptor (1166 A/C) and type 2 receptor (3123 C/A), and the BK-B2 receptor (-58T/C, exon 1) were analyzed and significant differences of genotypes and allelic frequencies in the AngII type 2 receptor C/A and BK-B2 receptor -58T/C were found between the essential hypertension and control subjects. Further, a significantly higher incidence of the C allele of the BK-B2 receptor was seen in AMI subjects with hypertension compared with those without hypertension. Genetic variations in the AngII and BK-B2 receptors could prove to be significant pathophysiological mechanisms affecting essential hypertension and AMI, and genetic differences appear to be a new risk factor for these conditions.
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高血压急性心肌梗死的遗传因素。
本研究评估了日本人群中血管紧张素II (AngII)受体和缓激素B2 (BK-B2)受体多态性对高血压和急性心肌梗死(AMI)的贡献:150名原发性高血压患者,150名AMI伴/不伴高血压患者,以及150名年龄和性别匹配的健康对照。分析了AngII 1型受体(1166 A/C)和2型受体(3123 C/A)以及BK-B2受体(-58T/C,外显子1)的多态性,发现AngII 2型受体C/A和BK-B2受体-58T/C的基因型和等位基因频率在原发性高血压患者与对照组之间存在显著差异。此外,AMI高血压患者BK-B2受体C等位基因的发生率明显高于无高血压患者。AngII和BK-B2受体的遗传变异可能是影响原发性高血压和AMI的重要病理生理机制,遗传差异似乎是这些疾病的一个新的危险因素。
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