Randomized, placebo-controlled trial of the angiotensin-converting enzyme inhibitor, ramipril, in patients with coronary or other occlusive arterial disease
S. Macmahon et al., Randomized, placebo-controlled trial of the angiotensin-converting enzyme inhibitor, ramipril, in patients with coronary or other occlusive arterial disease, J AM COL C, 36(2), 2000, pp. 438
Citations number
24
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
OBJECTIVES The primary objective of this study was to investigate the effec
ts of the angiotensin-converting enzyme (ACE) inhibitor, ramipril, on carot
id atherosclerosis in patients with coronary, cerebrovascular or peripheral
vascular disease.
BACKGROUND Angiotensin-converting enzyme inhibitors have been shown to redu
ce the risk of coronary events in various patient groups and to prevent the
development of atherosclerosis in animal models. It has been hypothesized
that the clinical benefits of ACE inhibitors may, therefore, be mediated by
effects on atherosclerosis.
METHODS Six hundred seventeen patients were randomized in equal proportions
to ramipril (5-10 mg daily) or placebo. At baseline, two years and four ye
ars, carotid atherosclerosis was assessed by B-mode ultrasound, and left ve
ntricular mass was assessed by Ill-mode echocardiography.
RESULTS Blood pressure (BP) was reduced by a mean of 6 mm Hg systolic and 4
mm Hg diastolic in the ramipril group compared with the placebo group (p <
0.001). There was no difference between groups in the changes in common ca
rotid artery wall thickness (p 0.58) or in carotid plaque (p = 0.93). Left
ventricular mass index decreased by 3.8 g/m(2) (4%) in the ramipril group c
ompared with the placebo group (2p = 0.04).
CONCLUSIONS The results provide no support for the hypothesis that reduced
atherosclerosis is responsible for the beneficial effects of ACE inhibitors
on major coronary events. It is more likely that the benefits are due to l
ower BP, reduced left ventricular mass or other factors such as reversal of
endothelial dysfunction. (C) 2000 by the American College of Cardiology.