EFFICACY OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A REDUCTASE INHIBITORS IN THE TREATMENT OF PATIENTS WITH HYPERCHOLESTEROLEMIA - A METAANALYSIS OF CLINICAL-TRIALS
Sxd. Kong et al., EFFICACY OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME-A REDUCTASE INHIBITORS IN THE TREATMENT OF PATIENTS WITH HYPERCHOLESTEROLEMIA - A METAANALYSIS OF CLINICAL-TRIALS, Clinical therapeutics, 19(4), 1997, pp. 778-797
Recent studies have documented the longterm impact of 3-hydroxy-3-meth
ylglutaryl coenzyme A (HMG-CoA) reductase inhibitors on mortality and
morbidity related to coronary heart disease, establishing the link bet
ween lowering cholesterol levels and reducing cardiac events. Our stud
y was a comparative Literature review and meta-analysis of the efficac
y of four HMG-CoA reductase inhibitors-fluvastatin, lovastatin, pravas
tatin, and simvastatin-used in the treatment of patients with hypercho
lesterolemia. The data sources for our meta-analysis of the efficacy o
f these cholesterol-lowering agents were 52 randomized, double-masked
clinical trials with at least 25 patients per treatment arm. The resul
ts showed all four agents to be effective in reducing blood cholestero
l levels. We computed summary efficacy estimates for all published dos
e strengths for the four agents. Fluvastatin 20 mg/d reduced low-densi
ty lipoprotein cholesterol (LDL-C) levels by 21.0% and total cholester
ol (total-C) levels by 16.4%; fluvastatin 40 mg/d reduced these levels
by 23.1% and 17.7%, respectively. Lovastatin 20 mg/d reduced LDL-C le
vels by 24.9% and total-C levels by 17.7%; lovastatin 80 mg/d reduced
these levels by 39.8% and 29.2%, respectively. Pravastatin 10 mg/d red
uced LDL-C levels by 19.3% and total-C levels by 14.0%; pravastatin 80
mg/d reduced these levels by 37.7% and 28.7%, respectively. Simvastat
in 2.5 mg/d reduced LDL-C levels by 22.9% and total-C levels by 15.7%;
simvastatin 40 mg/d reduced these levels by 40.7% and 29.7%, respecti
vely. The results of our meta-analysis can be used in conjunction with
treatment objectives and comparative cost-effectiveness data for thes
e agents to decide appropriate therapeutic alternatives for individual
patients.