Efficacy and Safety of Ezetimibe Added on to Atorvastatin (20 mg) Versus Uptitration of Atorvastatin (to 40 mg) in Hypercholesterolemic Patients at Moderately High Risk for Coronary Heart Disease

被引:68
作者
Conard, Scott E. [1 ]
Bays, Harold E. [2 ]
Leiter, Lawrence A. [3 ,4 ]
Bird, Steven R. [5 ]
Rubino, Joseph [5 ]
Lowe, Robert S. [5 ]
Tomassini, Joanne E. [5 ]
Tershakovec, Andrew M. [5 ]
机构
[1] Univ Texas SW Med Sch, Dallas, TX USA
[2] Louisville Metab & Atherosclerosis Res Ctr, Louisville, KY USA
[3] St Michaels Hosp, Toronto, ON M5B 1W8, Canada
[4] Univ Toronto, Toronto, ON, Canada
[5] Merck & Co Inc, N Wales, PA USA
关键词
D O I
10.1016/j.amjcard.2008.09.075
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of this study was to evaluate the efficacy and safety of ezetimibe 10 mg added to atorvastatin 20 mg compared with doubling atorvastatin to 40 mg in patients with hypercholesterolemia at moderately high risk for coronary heart disease who did not reach low-density lipoprotein (LDL) cholesterol levels <100 mg/dl with atorvastatin 20 mg. In this 6-week, multicenter, double-blind, randomized, parallel-group study, 196 patients treated with atorvastatin 20 mg received atorvastatin 20 mg plus ezetimibe 10 mg or atorvastatin 40 mg for 6 weeks. Adding ezetimibe 10 mg to atorvastatin 20 mg produced significantly greater reductions in LDL. cholesterol than increasing atorvastatin to 40 mg (-31% vs -11%, p <0.001). Significantly greater reductions were also seen in non-high-density lipoprotein cholesterol, total cholesterol, and apolipoprotein B (p <0.001). Significantly more patients reached LDL cholesterol levels < 1.00 mg/dl with atorvastatin 20 mg plus ezetimibe compared with atorvastatin 40 mg (84% vs 49%, p <0.001.). The 2 treatment groups had comparable results for high-density lipoprotein cholesterol, triglycerides, apolipoprotein A-I, and high-sensitivity C-reactive protein. The incidences of clinical and laboratory adverse experiences were generally similar between groups. In conclusion, the addition of ezetimibe 10 mg to atorvastatin 20 mg was generally well tolerated and resulted in significantly greater lipid-lowering efficacy compared with doubling atorvastatin to 40 mg in patients with hypercholesterolemia at moderately high risk for coronary heart disease. (C) 2008 Published by Elsevier Inc. (Am J Cardiol 2008;102:1489-1494)
引用
收藏
页码:1489 / 1494
页数:6
相关论文
共 14 条
[1]   Efficacy and safety of ezetimibe co-administered with simvastatin compared with atorvastatin in adults with hypercholesterolemia [J].
Ballantyne, CM ;
Blazing, MA ;
King, TR ;
Brady, WE ;
Palmisano, J .
AMERICAN JOURNAL OF CARDIOLOGY, 2004, 93 (12) :1487-1494
[2]   Effect of ezetimibe coadministered with atorvastatin in 628 patients with primary hypercholesterolemia - A prospective, randomized, double-blind trial [J].
Ballantyne, CM ;
Houri, J ;
Notarbartolo, A ;
Melani, L ;
Lipka, LJ ;
Suresh, R ;
Sun, S ;
LeBeaut, AP ;
Sager, PT ;
Veltri, EP .
CIRCULATION, 2003, 107 (19) :2409-2415
[3]  
Bays Harold E, 2008, Expert Rev Cardiovasc Ther, V6, P447, DOI 10.1586/14779072.6.4.447
[4]   Efficacy and safety of ezetimibe co-administered with atorvastatin in untreated patients with primary hypercholesterolaemia and coronary heart disease [J].
Blagden, M. D. ;
Chipperfield, R. .
CURRENT MEDICAL RESEARCH AND OPINION, 2007, 23 (04) :767-775
[5]   Reaching goal in hypercholesterolaemia: dual inhibition of cholesterol synthesis and absorption with simvastatin plus ezetimibe [J].
Daskalopoulou, SS ;
Mikhailidis, DP .
CURRENT MEDICAL RESEARCH AND OPINION, 2006, 22 (03) :511-528
[6]   Efficacy and safety of ezetimibe coadministered with statins: randomised, placebo-controlled, blinded experience in 2382 patients with primary hypercholesterolemia [J].
Davidson, MH ;
Ballantyne, CM ;
Kerzner, B ;
Melani, L ;
Sager, PT ;
Lipka, L ;
Strony, J ;
Suresh, R ;
Veltri, E .
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE, 2004, 58 (08) :746-755
[7]   Efficacy and safety of ezetimibe coadministered with simvastatin in patients with primary hypercholesterolemia: A randomized, double-blind, placebo-controlled trial [J].
Goldberg, AC ;
Sapre, A ;
Liu, J ;
Capece, R ;
Mitchel, YB .
MAYO CLINIC PROCEEDINGS, 2004, 79 (05) :620-629
[8]  
Grundy Scott M, 2004, J Am Coll Cardiol, V44, P720, DOI 10.1016/j.jacc.2004.07.001
[9]   Diagnosis and management of the metabolic syndrome - An American Heart Association/National Heart, Lung, and Blood Institute Scientific Statement [J].
Grundy, SM ;
Cleeman, JI ;
Daniels, SR ;
Donato, KA ;
Eckel, RH ;
Franklin, BA ;
Gordon, DJ ;
Krauss, RM ;
Savage, PJ ;
Smith, SC ;
Spertus, JA ;
Costa, F .
CIRCULATION, 2005, 112 (17) :2735-2752
[10]  
LEITER LA, 2008, AM J CARDIOL, V108, DOI DOI 10.1016/JAMJCARD.2008.08.076