期刊文献+

血管紧张素Ⅰ转换酶基因插入或缺失(ACE I/D)多态性与血管紧张素Ⅱ1型受体1166A/C基因(AT1R 1166A/C)多态性对川崎病(KD)患者局部缺血性心脏病可能的协同影响

Possible synergic effect of angiotensin-Ⅰ converting enzyme gene insertion/deletion polymorphism and angiotensin-n type-Ⅱ receptor 1166A/C gene polymorphism on is-chemic heart disease in patients with Kawasaki disease
下载PDF
导出
摘要 一般认为ACEI/D和AT1R1166A/C多态性是影响冠脉疾病发展的个体危险因素。作者试图寻找证据证明ACEI/D和AT1R1166A/C多态性对KD患者冠状动脉狭窄的影响。 ACE I/D and AT1R 1166A/C polymorphisms are considered to comprise individual risk factors for the development of coronary disease. We sought to demonstrate that the ACE I/D and AT1R 1166A/C polymorphisms affect coronary artery stenosis in patients with Kawasaki disease (KD) . We examined 147 healthy controls and 281 Japanese children with KD. The patients were further di- vided into group N (n=246, no ischemia) and group Ⅰ (n=35, severe coronary artery stenosis with myocardial ischemia), and we studied the genotype of ACE I/D and AT1R 1166A/C polymorphisms. We also examined ACE activity in patients with acute KD. We did not detect any prevalent genotypes of the ACE and AT1R polymorphisms between controls and KD patients. However, the prevalence of the D allele in the ACE polymorphism and of the C allele in the AT1R polymorphism tended to be higher in group Ⅰ than in group N (odds ratios, 2. 00 and 2. 32, respectively). In addition, the presence of the D and/or C alleles significantly increased the relative risk of developing myocardial ischemia (odds ratio, 2. 71; p=0. 038) . During the convalescent phase of KD, ACE activity was increased despite significant attenuation during the acute phase. These results suggested that the renin-angiotensin system is associated with the formation of severe coronary artery stenosis and myocardial ischemia.
  • 相关文献

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部