Angiotensin-converting-enzyme inhibition in stable coronary artery disease
- PMID: 15531767
- PMCID: PMC2556374
- DOI: 10.1056/NEJMoa042739
Angiotensin-converting-enzyme inhibition in stable coronary artery disease
Abstract
Background: Angiotensin-converting-enzyme (ACE) inhibitors are effective in reducing the risk of heart failure, myocardial infarction, and death from cardiovascular causes in patients with left ventricular systolic dysfunction or heart failure. ACE inhibitors have also been shown to reduce atherosclerotic complications in patients who have vascular disease without heart failure.
Methods: In the Prevention of Events with Angiotensin Converting Enzyme Inhibition (PEACE) Trial, we tested the hypothesis that patients with stable coronary artery disease and normal or slightly reduced left ventricular function derive therapeutic benefit from the addition of ACE inhibitors to modern conventional therapy. The trial was a double-blind, placebo-controlled study in which 8290 patients were randomly assigned to receive either trandolapril at a target dose of 4 mg per day (4158 patients) or matching placebo (4132 patients).
Results: The mean (+/-SD) age of the patients was 64+/-8 years, the mean blood pressure 133+/-17/78+/-10 mm Hg, and the mean left ventricular ejection fraction 58+/-9 percent. The patients received intensive treatment, with 72 percent having previously undergone coronary revascularization and 70 percent receiving lipid-lowering drugs. The incidence of the primary end point--death from cardiovascular causes, myocardial infarction, or coronary revascularization--was 21.9 percent in the trandolapril group, as compared with 22.5 percent in the placebo group (hazard ratio in the trandolapril group, 0.96; 95 percent confidence interval, 0.88 to 1.06; P=0.43) over a median follow-up period of 4.8 years.
Conclusions: In patients with stable coronary heart disease and preserved left ventricular function who are receiving "current standard" therapy and in whom the rate of cardiovascular events is lower than in previous trials of ACE inhibitors in patients with vascular disease, there is no evidence that the addition of an ACE inhibitor provides further benefit in terms of death from cardiovascular causes, myocardial infarction, or coronary revascularization.
Copyright 2004 Massachusetts Medical Society.
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Comment in
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ACE inhibitors for patients with vascular disease without left ventricular dysfunction--may they rest in PEACE?N Engl J Med. 2004 Nov 11;351(20):2115-7. doi: 10.1056/NEJMe048255. Epub 2004 Nov 7. N Engl J Med. 2004. PMID: 15531768 No abstract available.
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Adding ACE inhibitor doesn't improve outcomes in stable angina and normal LVEF.J Fam Pract. 2005 Feb;54(2):109, 113. J Fam Pract. 2005. PMID: 15689283 No abstract available.
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The PEACE trial: ACE inhibitors and coronary artery disease.Rev Cardiovasc Med. 2005 Winter;6(1):54-9. Rev Cardiovasc Med. 2005. PMID: 15741925 No abstract available.
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ACE inhibition in stable coronary artery disease.N Engl J Med. 2005 Mar 3;352(9):937-9; author reply 937-9. doi: 10.1056/NEJM200503033520919. N Engl J Med. 2005. PMID: 15745989 No abstract available.
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ACE inhibition in stable coronary artery disease.N Engl J Med. 2005 Mar 3;352(9):937-9; author reply 937-9. N Engl J Med. 2005. PMID: 15751128 No abstract available.
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ACE inhibition in stable coronary artery disease.N Engl J Med. 2005 Mar 3;352(9):937-9; author reply 937-9. N Engl J Med. 2005. PMID: 15751129 No abstract available.
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PEACE and CAMELOT.Prev Cardiol. 2005 Spring;8(2):127-9. doi: 10.1111/j.1520-037x.2005.4006.x. Prev Cardiol. 2005. PMID: 15860991 No abstract available.
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Trandolapril did not reduce cardiovascular death or other events in stable coronary artery disease.ACP J Club. 2005 May-Jun;142(3):66. ACP J Club. 2005. PMID: 15862065 No abstract available.
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Unique populations: different outcomes.Curr Cardiol Rep. 2005 May;7(3):155-6; discussion 156-8. Curr Cardiol Rep. 2005. PMID: 15865852 No abstract available.
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