Key result
Zofenopril cuts 1-year cardiovascular events ~30% compared to placebo and other ACE inhibitors.
Why the study?
Does zofenopril reduce the 1-year combined occurrence of death or hospitalization for cardiovascular causes in post-AMI patients compared to placebo or other ACE inhibitors, regardless of concomitant thiazide diuretic use?
Meta-Analysis (n=2,995)
Double-blind
Randomized
Does zofenopril reduce the 1-year combined occurrence of death or hospitalization for cardiovascular causes in post-AMI patients compared to placebo or other ACE inhibitors, regardless of concomitant thiazide diuretic use?
Effect estimate: HR 1.04 (95% CI 0.74-1.45)
Absolute Event Rate: 18.3% vs 16.8%
p-value: p=0.838
Zofenopril maintains its prognostic benefits in reducing 1-year cardiovascular events in post-AMI patients compared to placebo or other ACE inhibitors, regardless of concomitant thiazide diuretic use.
Zofenopril may warrant preference post-AMI; extends ACEI evidence independent of thiazide use.
Background: In the Survival of Myocardial Infarction Long-Term Evaluation (SMILE) studies, early administration of zofenopril after acute myocardial infarction (AMI) was prognostically beneficial as compared to placebo and other angiotensin-converting enzyme inhibitors (ACEIs), such as lisinopril and ramipril. Here, we investigated whether zofenopril efficacy could be affected by a concomitant use of thiazide diuretics (TDs). Methods: This was a post hoc analysis of pooled individual patient data from the SMILE studies. Patients treated with other diuretics than TDs were excluded. The primary study endpoint was the 1-year combined occurrence of death or hospitalization for CV causes, with or without TD. Results: Among 2,995 patients, 263 (8.8%) were treated with a combination including a TD (TD+), whereas 2,732 (91.2%) were not treated with any diuretic (TD-). Proportions of subjects who were treated with TD were equally distributed ( p =0.774) within the placebo, zofenopril, and other ACEIs groups. The 1-year risk of major cardiovascular events was similar in TD+ (18.3%) and TD- (16.8%) patients (hazard ratio [HR] 1.04; 95% CI 0.74–1.45; p =0.838). After stratifying per concomitant treatment and TD, the 1-year risk of CV events was significantly lower with zofenopril than with placebo (HR 0.70; 95% CI 0.55–0.88; p =0.002) and other ACEIs (HR 0.58; 95% CI 0.46–0.74; p =0.0001). Treatment with ACEIs and TD as concomitant therapy was associated with a larger blood pressure (BP) reduction ( p =0.0001 for systolic BP and p =0.045 for diastolic BP). Conclusion: In post AMI patients, zofenopril maintained its positive impact on prognosis compared to placebo or other ACEIs, regardless concomitant TD administration. In this setting, TD shows advantages in managing the most difficult hypertensive patients.
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Borghi et al. (2018) conducted a meta-analysis in Acute myocardial infarction (n=2,995). Thiazide diuretics (TD+) vs. No diuretics (TD-) was evaluated on 1-year combined occurrence of death or hospitalization for CV causes (HR 1.04, 95% CI 0.74-1.45, p=0.838). Zofenopril significantly reduced the 1-year risk of cardiovascular events compared to placebo (HR 0.70; 95% CI 0.55-0.88; p=0.002) and other ACEIs, regardless of concomitant thiazide diuretic use.
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