Effect of angiotensin-converting enzyme inhibition on restenosis after coronary stenting

被引:36
|
作者
Ribichini, F
Wins, W
Ferrero, V
Matullo, G
Camilla, T
Feola, M
Guarrera, S
Vado, A
Piazza, A
Uslenghi, E
机构
[1] Osped Santa Croce & Carle, Dept Cardiovasc Dis, I-12100 Cuneo, Italy
[2] Osped Santa Croce & Carle, Biochem Lab, I-12100 Cuneo, Italy
[3] Univ Piemonte Orientale, OSped Maggiore Carita, Div Cardiol, Novara, Italy
[4] Onze Lieve Vrouw Hosp, Ctr Cardiovasc, Aalst, Belgium
[5] Univ Turin, Dept Genet Biol & Biochem, Turin, Italy
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2003年 / 91卷 / 02期
关键词
D O I
10.1016/S0002-9149(02)03101-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The Plasma level of angiotensin-converting enzyme (ACE) has been identified as a major risk factor for restenosis after coronary stent implantation in selected patients; ACE inhibition may therefore contribute to prevent its occurrence. The effect of oral ACE inhibition at conventional doses was analyzed retrospectively in a series of 897 patients with ischemia who received greater than or equal to1 coronary stent on 998 lesions and underwent angiographic follow-up; no exclusion criteria were introduced in this analysis. The restenosis rate in 282 patients (31.4%) taking ACE inhibitors was 36.6% compared with 22.9% in 615 non-ACE-inhibited patients (p = 0.00001, odds ratio [OR] 1.94, 95% confidence interval [CI] 1.45 to 2.59), and the late loss in minimum lumen diameter was 1.25 +/- 0.8 versus 0.96 +/- 0.8 mm, respectively (p = 0.0001). During univariate analysis, a negative effect of the drug on restenosis was observed in all subgroups of patients (i.e., hypertensives, diabetics, women, and patients with previous myocardial infarction). Similar effects were observed independently of the ACE gene insertion/deletion polymorphism. During multivariate analysis, ACE inhibition was confirmed as an independent risk factor for restenosis (OR 1.84, 95% Cl 1.35 to 2.51, p = 0.0001). Other predictors were the implantation of multiple stents (OR 2.41, 95% Cl 1.60 to 3.64, p <0.0001), diabetes (OR 2.34, 95% Cl 1.61 to 3.41, p <0.0001), and vessel reference diameter before angioplasty (OR 0.51, 95% Cl 0.38 to 0.69, p <0.0001). Although unexplained and apparently contradictory, our data suggest that the use of conventional oral doses of ACE inhibitors in a "real-world" population who underwent coronary stent implantation increases the incidence of in-stent restenosis. Such a finding does not negate the known clinical benefits of ACE inhibitors, but it may deserve attention when a patient treated with ACE inhibitors becomes a candidate for stent implantation. (C) 2003 by Excerpta Medica, Inc.
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页码:154 / 158
页数:5
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