DECEMBER 15, 2004
VOLUME 1 NO. 23
 

An ACE up your sleeve doesn't even patients' survival odds

Trial shows heart drug isn't all it's cracked up to be, leaving
docs to pick up PEACEs


Years of cholesterol-laden fast food and couch-potato living have taken their toll on Eddy Velasquez. The 50-year-old has coronary artery disease (CAD). "My doc says my condition is stable," says Eddy. "Still, I'm plenty scared and want to do what I can to make things better. I've heard that ACE inhibitors may be good for someone like me." Eddy may be disappointed to hear the latest news on these drugs. A randomized study just published in the November 11 issue of the New England Journal of Medicine (NEJM) documents how angiotensin-converting enzyme (ACE) inhibitors, in particular trandolapril, commonly prescribed for the treatment of hypertension, don't benefit some folks with stable CAD.

PLAN FOR PEACE
ACE inhibitors are known to reduce such risks "in patients with left ventricular systolic dysfunction or heart failure," according to the authors of the NEJM study. As well, the drugs can minimize complications arising from fatty build-up on arterial walls in folks who have vascular disease but whose hearts are working satisfactorily. So Dr Eugene Braunwald of Boston's Harvard Medical School and colleagues from the Prevention of Events with Angiotensin Converting Enzyme Inhibition (PEACE) trial decided to see whether the addition of ACE inhibitors to conventional therapy would help low-risk patients. This group of individuals had stable CAD and a normal or only marginally reduced functioning of the heart's left ventricle.

The trial involved 8,290 patients with a mean age of 64 years. Seventy percent were taking drugs to curb their lipid levels and 72% had undergone coronary revascularization. Both the patients and the investigators were unaware who was receiving the ACE inhibitor trandolapril or placebo. Baseline measurements of mean blood pressure and heart function (left ventricular ejection) were established in all subjects. The rates of nonlethal heart attack, death due to a malfunctioning heart or blood vessels, and incidences where blocked blood vessels had to be reopened surgically, were noted over the course of the trial.

Over almost five years, 21.9% of the patients taking trandolapril died from coronary revascularization, heart attack, or other heart or blood vessel malfunctions. The death rate from these causes in the placebo group was pretty similar at 22.5%.

F-ACE THE MUSIC
"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's no evidence that the addition of an ACE inhibitor provides further benefit in terms of death from cardiovascular causes, myocardial infarction or coronary revascularization," conclude the authors of the NEJM paper.

However, they note "physicians may still wish to consider ACE inhibitor therapy for any patient who does not clearly fit the profile of patients in this trial." In an accompanying editorial, Dr Bertram Pitt, of the University of Michigan School of Medicine in Ann Arbor, describes the results as "surprising," given what's known about how ACE inhibitors work. As a result of the study, he says, "I will no longer recommend an ACE inhibitor to patients like those included in the PEACE trial."

 

 

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