Oike Y, Hata A, Ogata Y, Numata Y, Shido K, Kondo K
Department of Cardiology, Japanese Red Cross Kumamoto Hospital, Japan.
J Clin Invest. 1995 Dec;96(6):2975-9. doi: 10.1172/JCI118369.
It has been reported that individuals with the D allele of an insertion/deletion (I/D) polymorphism of the angiotensin converting enzyme (ACE) gene are at greater risk for myocardial infarction (MI), especially among subjects normally considered to be at low risk. However, little is known about the mechanism by which the ACE polymorphism affects the risk of MI. Coronary artery spasm (CAS) is considered to be one possible mechanism for developing MI. We therefore examined the ACE polymorphism relation to CAS to determine if this was the mechanism by which the DD genotype influences MI. We studied 150 angiographically assessed Japanese males, all more than 60 yr old. CASs were detected using intracoronary injection of ergonovine maleate. Subjects were divided into three groups: those with CAS (group 1), those without CAS, but with fixed organic stenosis (group 2); and those without CAS and no organic stenosis (group 3). DD subjects were significantly represented in group 1 when compared with groups 2 (P = 0.002) and 3 (P = 0.026). These results suggest that the DD genotype relates to the greater risk for MI in the patients with CAS.
据报道,血管紧张素转换酶(ACE)基因插入/缺失(I/D)多态性的D等位基因个体发生心肌梗死(MI)的风险更高,尤其是在通常被认为低风险的人群中。然而,关于ACE基因多态性影响MI风险的机制知之甚少。冠状动脉痉挛(CAS)被认为是发生MI的一种可能机制。因此,我们研究了ACE基因多态性与CAS的关系,以确定这是否是DD基因型影响MI的机制。我们研究了150名经血管造影评估的日本男性,均超过60岁。通过冠状动脉内注射马来酸麦角新碱检测CAS。受试者分为三组:有CAS的患者(第1组)、无CAS但有固定器质性狭窄的患者(第2组);无CAS且无器质性狭窄的患者(第3组)。与第2组(P = 0.002)和第3组(P = 0.026)相比,第1组中DD受试者显著更多。这些结果表明,DD基因型与CAS患者发生MI的较高风险相关。