医学
内科学
冲程(发动机)
心脏病学
基因型
血管紧张素转换酶
心肌梗塞
冠状动脉疾病
疾病
等位基因
风险因素
血压
基因
遗传学
工程类
生物
机械工程
作者
Kazuomi Kario,Nobuyuki Kanai,Ken Saito,Naoki Nago,Takefumi Matsuo,Kazuyuki Shimada
出处
期刊:Circulation
[Lippincott Williams & Wilkins]
日期:1996-05-01
卷期号:93 (9): 1630-1633
被引量:113
标识
DOI:10.1161/01.cir.93.9.1630
摘要
Background The ACE insertion/deletion ( I/D ) polymorphism is reported to be associated with myocardial infarction in both whites and Japanese. However, there have been no reports on the association of this polymorphism with stroke in each race. Furthermore, there are some racial differences in the demographics of cardiovascular diseases. In Japanese, stroke (especially that which occurs in preexisting hypertension) is more common and coronary artery disease much less common than in whites. We propose that the ACE I/D polymorphism might be associated with hypertensive cerebrovascular disease in Japanese. Methods and Results To study the association between the ACE I/D polymorphism and hypertensive cerebrovascular disease, we identified the ACE I/D genotype in 228 hypertensive and 104 normotensive Japanese subjects. Compared with its frequency (0.31) in the 90 hypertensives without lacunae detected by magnetic resonance imaging, the ACE*D allele frequency was significantly higher (0.47; P <.001) in the 138 hypertensives with silent or clinically overt ischemic stroke, whereas there was no significant difference between its frequency in hypertensives without lacunae and in 104 normotensive control subjects (0.34). The positive association between the ACE I/D genotype and ischemic stroke in hypertensive patients was independent of other risk factors. Conclusions We found a positive association between the ACE*D allele and ischemic stroke in Japanese hypertensives in our study. The ACE*D allele may be an independent risk factor for the development of cerebrovascular disease in hypertensive patients.
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