Ezetimibe coadministered with simvastatin in patients with primary hypercholesterolemia

被引:424
作者
Davidson, MH
McGarry, T
Bettis, R
Melani, L
Lipka, LJ
LeBeaut, AP
Suresh, R
Sun, S
Veltri, EP
机构
[1] Chicago Ctr Clin Res, Chicago, IL 60610 USA
[2] Oklahoma Fdn Cardiovasc Res, Oklahoma City, OK USA
[3] Edmonds Family Med Clin, Edmonds, WA USA
[4] Schering Plough Res Inst, Kenilworth, NJ USA
关键词
D O I
10.1016/S0735-1097(02)02610-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The purpose of this study was to assess the efficacy and safety of ezetimibe administered with simvastatin in patients with primary hypercholesterolemia. BACKGROUND Despite the availability of statins, many patients do not achieve lipid targets. Combination therapy with lipid-lowering agents that act via a complementary pathway may allow additional patients to achieve recommended cholesterol goals. METHODS After dietary stabilization, a 2- to 12-week washout period, and a 4-week, single-blind, placebo lead-in period, patients with baseline low-density lipoprotein cholesterol (LDL-C) greater than or equal to 145 mg/dl to less than or equal to 250 mg/dl and triglycerides (TG) less than or equal to 350 mg/dl were randomized to one of the following 10 groups administered daily for 12 consecutive weeks: ezetimibe 10 mg; simvastatin 10, 20, 40, or 80 mg; ezetimibe 10 mg plus simvastatin 10, 20, 40, or 80 mg; or placebo. The primary efficacy variable was percentage reduction from baseline to end point in direct LDL-C for the pooled ezetimibe plus simvastatin groups versus pooled simvastatin groups. RESULTS Ezetimibe plus simvastatin significantly improved LDL-C (p < 0.01), high-density lipoprotein cholesterol (HDL-C) (p = 0.03), and TG (p < 0.01) compared with sinivastatin alone. Ezetimibe plus simvastatin (pooled doses) provided an incremental 13.8% LDL-C reduction, 2.4% HDL-C increase, and 7.5% TG reduction compared with pooled sinivastatin alone. Coadministration of ezetimibe and simvastatin provided LDL-C reductions of 44% to 57%, TG reductions of 20% to 28%, and HDL-C increases of 8% to 11%, depending on the simvastatin dose. Ezetimibe 10 mg plus simvastatin 10 mg and simvastatin 80 mg alone each provided a 44% LDL-C reduction. The coadministration of ezetimibe with simvastatin was well tolerated, with a safety profile similar to those of sinivastatin and of placebo. CONCLUSIONS When coadministered with sinivastatin, ezetimibe provided significant incremental reductions in LDL-C and TG, as well as increases in HDL-C. Coadministration of ezetimibe with sinivastatin was well tolerated and comparable to statin alone. (C) 2002 by the American College of Cardiology Foundation.
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页码:2125 / 2134
页数:10
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