I. Taniguchi, T. Yamazaki, K. Wagatsuma, T. Kurusu, Y. Shimazu, K. Takikawa, M. Yoshikawa, S. Kageyama, S. Mochizuki
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引用次数: 27
摘要
支架植入术降低了冠状动脉介入治疗后再狭窄的发生率,但并没有完全消除再狭窄。本文研究了血管紧张素转换酶(ACE)基因型对冠状动脉支架植入术后冠状动脉疾病和再狭窄的影响。通过定量冠状动脉造影,在冠状动脉支架植入术前、植入术后和随访期间评估了103个成功植入支架的病变。DD、ID和II基因型患者的分布分别为13%、54%和33%。DD基因型的多血管疾病患病率明显较高(DD基因型:78%;ID基因型:58%;II基因型:27%,chi2=8.13, p=0.016), DD基因型晚期损失(1.43+/-0.96 mm)显著大于DD基因型(ID基因型:0.78+/-0.98 mm, II基因型:0.79+/-0.88 mm, p<0.05)。3个基因型的再狭窄率差异无统计学意义。目前在日本患者中的研究表明,DD基因型与更广泛的冠状动脉疾病和支架病变内向内重塑的进展有关,这主要是由内膜增生引起的。
The DD genotype of angiotensin converting enzyme polymorphism is a risk factor for coronary artery disease and coronary stent restenosis in Japanese patients.
Stent implantation has decreased the incidence of restenosis after coronary intervention, but has not eliminated it. The contribution of the angiotensin-converting enzyme (ACE) genotype to the development of coronary artery disease and restenosis after coronary stenting was investigated in 67 Japanese patients in whom 103 lesions in which stents had been successfully implanted were assessed by quantitative coronary angiography, before, immediately after coronary stenting, and during follow-up. The distribution of the patients with the DD, ID, and II genotypes was 13%, 54%, and 33%, respectively. The prevalence of multivessel disease in the DD genotype was significantly higher (DD genotype: 78%; ID genotype: 58%; II genotype: 27%, chi2=8.13, p=0.016) and the late loss in the DD genotype (1.43+/-0.96 mm) was significantly greater (ID genotype: 0.78+/-0.98 mm and II genotype: 0.79+/-0.88 mm, p<0.05 vs DD genotype). However, there was no significant difference in the restenosis rate among the 3 genotypes. The present study in Japanese patients indicates that the DD genotype is associated with more extensive coronary artery disease and progression of the inward remodeling within the stented lesion, which is primarily caused by neointimal hyperplasia.