Comparison of the efficacy and safety of rosuvastatin 10 mg and atorvastatin 20 mg in high-risk patients with hypercholesterolemia -: Prospective study to evaluate the Use of Low doses of the Statins Atorvastatin and Rosuvastatin (PULSAR)

被引:55
作者
Clearfield, Michael B.
Amerena, John
Bassand, Jean-Pierre
Hernandez Garcia, Hugo R.
Miller, Sam S.
Sosef, Froukje F. M.
Palmer, Michael K.
Bryzinski, Brian S.
机构
[1] Univ N Texas, Hlth Sci Ctr, Ft Worth, TX USA
[2] Univ Melbourne, Dept Clin & Biomed Sci, Melbourne, Vic, Australia
[3] Univ Hosp Besancon, Besancon, France
[4] Hosp Especialidades Ctr Med La Raza, Ctr Med Occident, Guadalajara, Jalisco, Mexico
[5] SAM Clin Res Ctr, San Antonio, TX USA
[6] AstraZeneca, Macclesfield, Cheshire, England
[7] AstraZeneca, Wilmington, DE USA
关键词
D O I
10.1186/1745-6215-7-35
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Many patients at high risk of cardiovascular disease do not achieve recommended low-density lipoprotein cholesterol (LDL-C) goals. This study compared the efficacy and safety of low doses of rosuvastatin (10 mg) and atorvastatin (20 mg) in high-risk patients with hypercholesterolemia. Methods: A total of 996 patients with hypercholesterolemia (LDL-C >= 3.4 and < 5.7 mmol/ L [130 and 220 mg/dL]) and coronary heart disease (CHD), atherosclerosis, or a CHD-risk equivalent were randomized to once-daily rosuvastatin 10 mg or atorvastatin 20 mg. The primary endpoint was the percentage change from baseline in LDL-C levels at 6 weeks. Secondary endpoints included LDL-C goal achievement (National Cholesterol Education Program Adult Treatment Panel III [NCEP ATP III] goal < 100 mg/dL; 2003 European goal < 2.5 mmol/ L for patients with atherosclerotic disease, type 2 diabetes, or at high risk of cardiovascular events, as assessed by a Systematic COronary Risk Evaluation (SCORE) risk = 5% or 3.0 mmol/ L for all other patients), changes in other lipids and lipoproteins, cost-effectiveness, and safety. Results: Rosuvastatin 10 mg reduced LDL-C levels significantly more than atorvastatin 20 mg at week 6 (44.6% vs. 42.7%, p < 0.05). Significantly more patients achieved NCEP ATP III and 2003 European LDL-C goals with rosuvastatin 10 mg compared with atorvastatin 20 mg (68.8% vs. 62.5%, p < 0.05; 68.0% vs. 63.3%, p < 0.05, respectively). High-density lipoprotein cholesterol was increased significantly with rosuvastatin 10 mg versus atorvastatin 20 mg (6.4% vs. 3.1%, p < 0.001). Lipid ratios and levels of apolipoprotein A-l also improved more with rosuvastatin 10 mg than with atorvastatin 20 mg. The use of rosuvastatin 10 mg was also cost-effective compared with atorvastatin 20 mg in both a US and a UK setting. Both treatments were well tolerated, with a similar incidence of adverse events (rosuvastatin 10 mg, 27.5%; atorvastatin 20 mg, 26.1%). No cases of rhabdomyolysis, liver, or renal insufficiency were recorded. Conclusion: In high-risk patients with hypercholesterolemia, rosuvastatin 10 mg was more efficacious than atorvastatin 20 mg at reducing LDL-C, enabling LDL-C goal achievement and improving other lipid parameters. Both treatments were well tolerated.
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