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Volume 6 Issue 166 Published - 14:00 UTC 08:00 EST 14-Jun-2004 Next Update - 14:00 UTC 08:00 EST 15-Jun-2004
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Efficacy and safety of ezetimibe coadministered with simvastatin in patients with primary hypercholesterolemia

Ezetimibe (Zetia), a relatively recent lipid-lowering drug, inhibits intestinal absorption of cholesterol. In a previous trial, ezetimibe plus simvastatin lowered cholesterol more than either drug alone. A newer trial examined the combination for a second time. The second study was sponsored by the maker of both drugs, which also employed four of the five authors.

Researchers randomized 887 patients (LDL cholesterol level, 145-250 mg/dL) to receive daily placebo, ezetimibe (10 mg), simvastatin (10, 20, 40, or 80 mg), or ezetimibe plus simvastatin (at the same four doses). At 12 weeks, LDL cholesterol levels decreased by 20% with ezetimibe alone, by 31% to 46% with simvastatin alone (in dose-response fashion), and by 46% to 61% with combination therapy (in dose-response fashion).

Combination therapy did not raise HDL cholesterol levels any better than monotherapy with either drug. A threefold or greater increase in serum transaminase (AST or ALT) levels occurred in 6 combination-therapy patients (2%) but in no monotherapy or placebo patients; transaminase levels normalized in all patients after the drugs were discontinued. At least 10-fold elevations of serum creatine kinase occurred in 3 statin recipients, but no cases of clinical myopathy were reported.

Ezetimibe is not as potent as simvastatin when taken alone, but combination therapy clearly is more potent than either monotherapy for lowering LDL cholesterol levels. Longer-term safety studies and trials with clinical endpoints are necessary for both for ezetimibe alone and for combination therapy.

MEDLINE:

Efficacy and safety of ezetimibe coadministered with simvastatin in patients with primary hypercholesterolemia: a randomized, double-blind, placebo-controlled trial.

Goldberg AC, Sapre A, Liu J, Capece R, Mitchel YB; Ezetimibe Study Group.

Lipid Research Clinic, Washington University, St Louis, MO 63110-1093, USA. agoldber@im.wustl.edu

OBJECTIVE: To compare the efficacy and safety of 10 mg of ezetimibe coadministered with simvastatin with the safety and efficacy of simvastatin monotherapy for patients with hypercholesterolemia. PATIENTS AND METHODS: This multicenter double-blind, placebo-controlled, factorial study enrolled 887 patients with hypercholesterolemia (low-density lipoprotein cholesterol [LDL-C], 145-250 mg/dL; triglycerides, < or = 350 mg/dL). Patients were randomized to 1 of 10 treatments--placebo, ezetimibe at 10 mg/d, simvastatin at 10, 20, 40, or 80 mg/d, or simvastatin at 10, 20, 40, or 80 mg/d plus ezetimibe at 10 mg/d for 12 weeks. The study began March 13, 2001, and ended January 8, 2002. The primary efficacy end point was the mean percent change in LDL-C levels from baseline to study end point (last available postbaseline LDL-C measurement) for the pooled ezetimibe/simvastatin group vs the pooled simvastatin monotherapy group. RESULTS: Coadministration of ezetimibe/simvastatin was significantly (P<.001) more effective than simvastatin alone in reducing LDL-C levels for the pooled ezetimibe/simvastatin vs pooled simvastatin analysis and at each specific dose comparison. The decrease in LDL-C levels with coadministration of ezetimibe and the lowest dose of simvastatin, 10 mg, was similar to the decrease with the maximum dose of simvastatin, 80 mg. A significantly (P<.001) greater proportion of patients in the ezetimibe/simvastatin group achieved target LDL-C levels compared with those in the monotherapy group. Treatment with ezetimibe/simvastatin also led to greater reductions in total cholesterol, triglyceride, non-high-density lipoprotein cholesterol, and apolipoprotein B levels compared with simvastatin alone; both treatments increased high-density lipoprotein cholesterol levels similarly. The safety and tolerability profiles for the ezetimibe/simvastatin and monotherapy groups were similar. CONCLUSION: Through dual inhibition of cholesterol absorption and synthesis, coadministration of ezetimibe/simvastatin offers a highly efficacious and well-tolerated lipid-lowering strategy for treating patients with primary hypercholesterolemia.

Publication Types:

  • Clinical Trial
  • Multicenter Study
  • Randomized Controlled Trial

PMID: 15132403 [PubMed - indexed for MEDLINE]

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