Borghi Claudio, Ambrosioni Ettore
Department of Medicine, University of Bologna, Bologna, Italy.
Am Heart J. 2007 Mar;153(3):445.e7-14. doi: 10.1016/j.ahj.2006.12.005.
The aim of the study was to investigate the cardioprotective effects of the angiotensin-converting enzyme inhibitor zofenopril in post-myocardial infarction (MI) patients with preserved left ventricular function (LVF).
Three hundred forty-nine post-MI patients with preserved LVF (LV ejection fraction >40%) were treated for 6 months with zofenopril 30 to 60 mg (n = 177) or placebo (n = 172) according to a double-blind, randomized study design. The primary end point of the study was the combined occurrence of significant ST-T abnormalities on ambulatory electrocardiography (ECG), ECG abnormalities or symptoms of angina during standard exercise test, recurrence of MI, and need for revascularization procedures for angina.
The primary end point occurred in 20.3% of zofenopril-treated and 35.9% of placebo-treated patients (P = .001), despite no differences in blood pressure control, LVF, and concomitant therapy. ST-T depression during ambulatory ECG occurred in 22.7% of patients treated with placebo and 10.7% of those undergoing ACE-inhibition treatment (P = .027). ST-T depression in response to exercise test occurred in 14.2% and 26.7% of patients treated with zofenopril or placebo, respectively, (P = .024), with a lower proportion of zofenopril-treated patients who complained of anginal pain (4.7 vs 14.3%; P = .017), significant ST depression (14.2 vs 26.7%; P = .024), and major ventricular arrhythmias (3.8 vs 10.5%; P = .048). The rate of major cardiovascular events was reduced in patients treated with ACE inhibitor, with a lower rate of development and progression of congestive heart failure.
The results of the SMILE-ISCHEMIA study support the cardioprotective role of zofenopril when given to patients with normal LVF after acute MI.
本研究旨在探讨血管紧张素转换酶抑制剂佐芬普利对急性心肌梗死后左心室功能正常患者的心脏保护作用。
根据双盲随机研究设计,对349例急性心肌梗死后左心室功能正常(左心室射血分数>40%)的患者进行了为期6个月的治疗,其中177例患者服用30至60毫克佐芬普利,172例患者服用安慰剂。本研究的主要终点是动态心电图(ECG)出现显著ST-T异常、标准运动试验时出现ECG异常或心绞痛症状、心肌梗死复发以及因心绞痛需要进行血管重建手术的综合发生率。
尽管在血压控制、左心室功能和联合治疗方面没有差异,但主要终点在佐芬普利治疗组中的发生率为20.3%,在安慰剂治疗组中的发生率为35.9%(P = 0.001)。动态心电图期间ST-T压低在安慰剂治疗的患者中发生率为22.7%,在接受ACE抑制治疗的患者中发生率为10.7%(P = 0.027)。运动试验时ST-T压低在佐芬普利治疗组和安慰剂治疗组患者中的发生率分别为14.2%和26.7%(P = 0.024),佐芬普利治疗组中抱怨心绞痛疼痛的患者比例较低(4.7%对14.3%;P = 0.017),显著ST压低(14.2%对26.7%;P = 0.024)和主要室性心律失常(3.8%对10.5%;P = 0.048)。接受ACE抑制剂治疗的患者主要心血管事件发生率降低,充血性心力衰竭的发生和进展率较低。
SMILE-ISCHEMIA研究结果支持急性心肌梗死后左心室功能正常的患者服用佐芬普利具有心脏保护作用。