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血管紧张素I转换酶(ACE)基因DD基因型患者冠状动脉支架置入术后的ACE抑制剂与再狭窄

Angiotensin I-converting enzyme (ACE) inhibitors and restenosis after coronary artery stenting in patients with the DD genotype of the ACE gene.

作者信息

Koch Werner, Mehilli Julinda, von Beckerath Nicolas, Böttiger Corinna, Schömig Albert, Kastrati Adnan

机构信息

Deutsches Herzzentrum München, Experimentelle Kardiologie, Technische Universität München, Lazarettstrasse 36, D-80636 Munich, Germany.

出版信息

J Am Coll Cardiol. 2003 Jun 4;41(11):1957-61. doi: 10.1016/s0735-1097(03)00406-6.

Abstract

OBJECTIVES

We tested the hypothesis that patients with the DD genotype of the angiotensin I-converting enzyme (ACE) gene who are treated with ACE inhibitors are at a higher risk of restenosis after coronary stent placement than patients who do not receive ACE inhibitors.

BACKGROUND

Two recent studies with a limited series of patients carrying the DD genotype suggested an unfavorable impact of the use of ACE inhibitors on the restenotic process after implantation of stents in coronary arteries. Because these findings may question the use of ACE inhibitors after coronary stenting, we examined this important issue in a large series of patients.

METHODS

We determined the ACE gene I/D genotype of 2,222 consecutive patients with symptomatic coronary artery disease who underwent stent implantation. The patients with the DD genotype (n = 612) constituted the study population. The primary end point was in-stent restenosis, which was assessed as angiographic restenosis (> or =50% diameter stenosis at six-month follow-up) and clinical restenosis (need for target vessel revascularization due to symptoms or signs of ischemia in the presence of angiographic restenosis over one year after the intervention).

RESULTS

Of the 612 patients with the DD genotype, 403 (65.8%) were treated with ACE inhibitors and 209 (34.2%) did not receive ACE inhibitors. The angiographic and clinical restenosis rates were not significantly different between the group treated with ACE inhibitors and the group not receiving ACE inhibitors (p = 0.55). Continuous measures of restenosis, minimal lumen diameter, diameter stenosis, late lumen loss, and loss index were also similar in both groups (p > or = 0.55). In addition, one-year survival free of myocardial infarction was not significantly different between the two groups (p = 0.27).

CONCLUSIONS

In contrast to previous reports, our study provides evidence that patients carrying the DD genotype are not exposed to an increased risk of restenosis after stent placement when treated with ACE inhibitors.

摘要

目的

我们检验了这样一个假设,即与未接受血管紧张素转换酶(ACE)抑制剂治疗的患者相比,接受ACE抑制剂治疗的ACE基因DD基因型患者在冠状动脉支架置入术后发生再狭窄的风险更高。

背景

最近两项针对携带DD基因型的有限患者系列研究表明,使用ACE抑制剂对冠状动脉支架植入术后的再狭窄过程有不利影响。由于这些发现可能会对冠状动脉支架置入术后使用ACE抑制剂提出质疑,我们在大量患者中研究了这个重要问题。

方法

我们确定了2222例有症状冠状动脉疾病并接受支架植入术的连续患者的ACE基因I/D基因型。DD基因型患者(n = 612)构成研究人群。主要终点是支架内再狭窄,通过血管造影再狭窄(随访6个月时直径狭窄≥50%)和临床再狭窄(干预后1年以上,因缺血症状或体征且存在血管造影再狭窄而需要对靶血管进行血运重建)进行评估。

结果

在612例DD基因型患者中,403例(65.8%)接受了ACE抑制剂治疗,209例(34.2%)未接受ACE抑制剂治疗。接受ACE抑制剂治疗组与未接受ACE抑制剂治疗组的血管造影和临床再狭窄率无显著差异(p = 0.55)。两组在再狭窄的连续测量指标、最小管腔直径、直径狭窄、晚期管腔丢失和丢失指数方面也相似(p≥0.55)。此外,两组1年无心肌梗死生存率无显著差异(p = 0.27)。

结论

与之前的报道相反,我们的研究提供了证据表明,携带DD基因型的患者在接受ACE抑制剂治疗后,支架置入术后发生再狭窄的风险并未增加。

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