Effects of maximal doses of atorvastatin versus rosuvastatin on small dense low-density lipoprotein cholesterol levels

被引:47
作者
Ai, Masumi [1 ,2 ,3 ]
Otokozawa, Seiko [1 ,2 ,3 ]
Asztalos, Bela F. [1 ,2 ,3 ]
Nakajima, Katsuyuki [1 ,2 ,3 ]
Stein, Evan [4 ]
Jones, Peter H. [5 ]
Schaefer, Ernst J. f [1 ,2 ,3 ]
机构
[1] Tufts Univ, Friedman Sch Nutr Sci & Policy, Cardiovasc Res Lab, Boston, MA 02111 USA
[2] Tufts Univ, Sch Med, Boston, MA 02111 USA
[3] Tufts Univ, Lipid Metab Lab, Jean Mayer USDA Human Nutr Res Ctr Aging, Boston, MA 02111 USA
[4] Metab & Atherosclerosis Res Ctr, Cincinnati, OH USA
[5] Baylor Coll Med, Houston, TX 77030 USA
关键词
D O I
10.1016/j.amjcard.2007.08.035
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Maximal doses of atorvastatin and rosuvastatin are highly effective in lowering low-density lipoprotein (LDL) cholesterol and triglyceride levels; however, rosuvastatin has been shown to be significantly more effective than atorvastatin in lowering LDL cholesterol and in increasing high-density lipoprotein (HDL) and its subclasses. Our purpose in this post hoc subanalysis of an open-label study was to compare the effects of daily oral doses of rosuvastatin 40 mg with atorvastatin 80 mg over a 6-week period on direct LDL cholesterol and small dense LDL (sdLDL) cholesterol in 271 hyperlipidemic men and women versus baseline values. Rosuvastatin was significantly (p < 0.01) more effective than atorvastatin in decreasing sdLDL cholesterol (-53% vs -46%), direct LDL cholesterol (-52% vs -50%), total cholesterol/HDL cholesterol ratio (-46% vs -39%), and non-HDL cholesterol (-51 % vs -48%), The magnitude of these differences was modest, and the 2 statins caused similar decreases in triglyceride levels (-24% and -26%). In conclusion, our data indicate that the 2 statins, given at their maximal doses, significantly and beneficially alter the entire spectrum of lipoprotein particles, but that rosuvastatin is significantly more effective than atorvastatin in lowering direct LDL cholesterol and sdLDL cholesterol. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:315 / 318
页数:4
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