G. Reynolds et al., WHAT HAVE THE ACE-INHIBITOR TRIALS IN POSTMYOCARDIAL PATIENTS WITH LEFT-VENTRICULAR DYSFUNCTION TAUGHT US, European Journal of Clinical Pharmacology, 49, 1996, pp. 35-39
A series of elegant experimental studies and careful clinical observat
ion over a decade or more have led to the concept of 'infarct expansio
n' and 'remodelling' of the heart, culminating in a number of major mo
rtality studies indicating the effectiveness of angiotensin-converting
enzyme (ACE) inhibitors in patients after myocardial infarction (MI).
But has this concept been too narrow in predicting which patients mig
ht benefit from treatment with ACE inhibitors? Measurable infarct-expa
nsion with progressive dilatation probably occurs in less than 20% of
patients, whereas increase in volume and hypertrophy of the heart as r
esponses to compromised function are likely wherever significant myoca
rdial damage has occurred. Irrespective of infarct expansion, cumulati
ve extensive damage can lead to an inevitable downward spiral with gro
ss ventricular dilatation and death in heart failure. But in the major
ity of patients after MI a 'new equilibrium' is established in which i
nitial dilatation and subsequently hypertrophy restore adequate functi
on. Is it possible to distinguish patients in whom the cost and inconv
enience of long-term therapy with an ACE inhibitor justify the likely
benefit from treatment after an MI? The SAVE, AIRE and recent TRACE st
udies allow a rational approach for the clinician, indicating the effe
ctiveness of these drugs in patients with evidence of impaired ventric
ular function. However, the prospect that ACE inhibitors prescribed lo
ng term might also prevent myocardial reinfarction could justify wider
use. Post-MI patients are an easily identifiable high-risk group for
a cost-effective programme of secondary prevention. Reinfarction in an
already damaged ventricle carries a particularly poor prognosis and i
ts prevention by ACE inhibitors could make a major contribution to the
undoubted benefit from these agents. The recently completed TRACE stu
dy with its long-term follow-up may help resolve this issue, which is
also being investigated in a number of long-term prospective studies i
n populations at high risk of cardiovascular disease.