EFFECTS OF L-CARNITINE ADMINISTRATION ON LEFT-VENTRICULAR REMODELING AFTER ACUTE ANTERIOR MYOCARDIAL-INFARCTION - THE E-ECOCARDIOGRAFIA-DIGITALIZZATA-INFARTO-MIOCARDICO (CEDIM) TRIAL
S. Iliceto et al., EFFECTS OF L-CARNITINE ADMINISTRATION ON LEFT-VENTRICULAR REMODELING AFTER ACUTE ANTERIOR MYOCARDIAL-INFARCTION - THE E-ECOCARDIOGRAFIA-DIGITALIZZATA-INFARTO-MIOCARDICO (CEDIM) TRIAL, Journal of the American College of Cardiology, 26(2), 1995, pp. 380-387
Objectives. This study was performed to evaluate the effects of L-carn
itine administration on long-term left ventricular dilation in patient
s with acute anterior myocardial infarction. Background. Carnitine is
a physiologic compound that performs an essential role in myocardial e
nergy production at the mitochondrial level. Myocardial carnitine depr
ivation occurs during ischemia, acute myocardial infarction and cardia
c failure. Experimental studies have suggested that exogenous carnitin
e administration during these events has a beneficial effect on functi
on. Methods. The L-Carnitine Ecocardiografia Digitalizzata Infarto Mio
cardico (CEDIM) trial was a randomized, double-blind, placebo-controll
ed, multicenter trial in which 472 patients with a first acute myocard
ial infarction and high quality two-dimensional echocardiograms receiv
ed either placebo (239 patients) or L-carnitine (233 patients) within
24 h of onset of chest pain. placebo or L-carnitine was given at a dos
e of 9 g/day intravenously for the first 5 days and then 6 g/day orall
y for the next 12 months. Left ventricular volumes and ejection fracti
on were evaluated on admission, at discharge from hospital and at 3, 6
and 12 months after acute myocardial infarction. Results. A significa
nt attenuation of left ventricular dilation in the first year after ac
ute myocardial infarction was observed in patients treated with L-carn
itine compared with those receiving placebo. The percent increase in b
oth end diastolic and end-systolic volumes from admission to 3-, 6- an
d 12-month evaluation was significantly reduced in the L-carnitine gro
up. No significant differences were observed in left ventricular eject
ion fraction changes over time in the two groups. Although not designe
d to demonstrate differences in clinical end points, the combined inci
dence of death and congestive heart failure after discharge was 14 (6%
) in the L-carnitine treatment group versus 23 (9.6%) in the placebo g
roup (p = NS). Incidence of ischemic events during follow-up was simil
ar in the two groups of patients. Conclusions. L-Carnitine treatment i
nitiated early after acute myocardial infarction and continued for 12
months can attenuate left ventricular dilation during the first year a
fter an acute myocardial infarction, resulting in smaller left ventric
ular volumes at 3, 6 and 12 months after the emergent event.