Meta-analysis of Comparative Efficacy of Increasing Dose of Atorvastatin Versus Rosuvastatin Versus Simvastatin on Lowering Levels of Atherogenic Lipids (from VOYAGER)

被引:236
作者
Nicholls, Stephen J. [1 ,2 ,3 ]
Brandrup-Wognsen, Gunnar [4 ,5 ]
Palmer, Mike [6 ]
Barter, Philip J. [7 ]
机构
[1] Cleveland Clin, Dept Cardiovasc Med, Cleveland, OH 44106 USA
[2] Cleveland Clin, Dept Cell Biol, Cleveland, OH 44106 USA
[3] Cleveland Clin, Ctr Cardiovasc Diagnost & Prevent, Cleveland, OH 44106 USA
[4] AstraZeneca, Gothenburg, Sweden
[5] Univ Gothenburg, Dept Mol & Clin Med, Gothenburg, Sweden
[6] Keele Univ, Keele, Staffs, England
[7] Heart Res Inst, Sydney, NSW, Australia
关键词
CORONARY ATHEROSCLEROSIS; PRAVASTATIN; THERAPY; SAFETY;
D O I
10.1016/j.amjcard.2009.08.651
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Statins are the most commonly prescribed agents for lowering levels of low-density lipoprotein (LDL) cholesterol. Although dose-dependent reductions in levels of atherogenic lipids are observed with all statins, the impact of increasing dose has not been fully elucidated. An individual patient data pooled analysis was performed of 32,258 patients in studies comparing the efficacy of rosuvastatin with that of atorvastatin or simvastatin. The impact of increasing dose on lowering LDL cholesterol, triglycerides, non-high-density lipoprotein (HDL) cholesterol, and apolipoprotein B was investigated. Doubling the dose of each statin was accompanied by a 4% to 7% greater degree of lowering of all atherogenic lipids. A stronger correlation was observed between changes in LDL cholesterol and non-HDL cholesterol (r = 0.92, p <0.001) or apolipoprotein B (r = 0.76, p <0.001) than I riglycerides (r = 0.14, p <0.001). On multivariate analysis, baseline lipid level (p <0.0001) and increasing statin dose (p <0.0001) were strong predictors of achieving treatment goals in high-risk patients. Increasing age was a strong independent predictor of achieving goal for all atherogenic lipids (p <0.0001). Achieving LDL cholesterol goals was also more likely in women (p <0.0001), patients with diabetes (p <0.0001), and patients without atherosclerotic disease (p = 0.0002). In contrast, normal triglyceride levels were more often observed in men (p <0.0001) and patients without diabetes mellitus (p = 0.03). In conclusion, doubling statin dose was associated with greater lowering of LDL cholesterol by 4% to 6% and non-HDL cholesterol by 3% to 6%. Greater lipid goal achievement with increasing dose supports the use of high-dose statin therapy for more effective cardiovascular prevention. (C) 2010 Published by Elsevier Inc. (Am J Cardiol 2010;105:69-76)
引用
收藏
页码:69 / 76
页数:8
相关论文
共 14 条
[1]  
Brown H, 2015, Applied mixed models in medicine
[2]   Intensive versus moderate lipid lowering with statins after acute coronary syndromes [J].
Cannon, CP ;
Braunwald, E ;
McCabe, CH ;
Rader, DJ ;
Rouleau, JL ;
Belder, R ;
Joyal, SV ;
Hill, KA ;
Pfeffer, MA ;
Skene, AM .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (15) :1495-1504
[3]   European guidelines on cardiovascular disease prevention in clinical practice -: Third Joint Task Force of European and other Societies on Cardiovascular Disease Prevention in Clinical Practice [J].
De Backer, G ;
Ambrosioni, E ;
Borch-Johnsen, K ;
Brotons, C ;
Cifkova, R ;
Dallongeville, J ;
Ebrahim, S ;
Faergeman, O ;
Graham, I ;
Mancia, G ;
Cats, VM ;
Orth-Gomér, K ;
Perk, J ;
Pyörälä, K ;
Rodicio, JL ;
Sans, S ;
Sansoy, V ;
Sechtem, U ;
Silber, S ;
Thomsen, T ;
Wood, D .
EUROPEAN HEART JOURNAL, 2003, 24 (17) :1601-1610
[4]   Identification of genetic variants in endothelial lipase in persons with elevated high-density lipoprotein cholesterol [J].
deLemos, AS ;
Wolfe, ML ;
Long, CJ ;
Sivapackianathan, R ;
Rader, DJ .
CIRCULATION, 2002, 106 (11) :1321-1326
[5]   Comparison of the efficacy and safety of atorvastatin initiated at different starting doses in patients with dyslipidemia [J].
Jones, PH ;
McKenney, JM ;
Karalis, DG ;
Downey, J .
AMERICAN HEART JOURNAL, 2005, 149 (01) :e1
[6]   Effects of rosuvastatin versus atorvastatin, simvastatin, and pravastatin on non-high-density lipoprotein cholesterol, apolipoproteins, and lipid ratios in patients with hypercholesterolemia: Additional results from the STELLAR trial [J].
Jones, PH ;
Hunninghake, DB ;
Ferdinand, KC ;
Stein, EA ;
Gold, A ;
Caplan, RJ ;
Blasetto, JW .
CLINICAL THERAPEUTICS, 2004, 26 (09) :1388-1399
[7]   Comparison of the efficacy and safety of rosuvastatin versus atorvastatin, simvalstaltin, and pravastatin across doses (STELLAR* trial) [J].
Jones, PH ;
Davidson, MH ;
Stein, EA ;
Bays, HE ;
McKenney, JM ;
Miller, E ;
Cain, VA ;
Blasetto, JW ;
STELLAR Study Grp .
AMERICAN JOURNAL OF CARDIOLOGY, 2003, 92 (02) :152-160
[8]   Intensive lipid lowering with atorvastatin in patients with stable coronary disease [J].
LaRosa, JC ;
Grundy, SM ;
Waters, DD ;
Shear, C ;
Barter, P ;
Fruchart, J ;
Gotto, AM ;
Greten, H ;
Kastelein, JJP ;
Shepherd, J ;
Wenger, NK .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (14) :1425-1435
[9]   Effects of statins on 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibition beyond low-density lipoprotein cholesterol [J].
Liao, JK .
AMERICAN JOURNAL OF CARDIOLOGY, 2005, 96 (5A) :24F-33F
[10]   Comparison of the efficacy of rosuvastatin versus atorvastatin, simvastatin, and pravastatin in achieving lipid goals: results from the STELLAR trial [J].
McKenney, JM ;
Jones, PH ;
Adamczyk, MA ;
Cain, VA ;
Bryzinski, BS ;
Blasetto, JW .
CURRENT MEDICAL RESEARCH AND OPINION, 2003, 19 (08) :689-698