Multicenter collaborative randomized parallel group comparative study of pitavastatin and atorvastatin in Japanese hypercholesterolemic patients Collaborative study on hypercholesterolemia drug intervention and their benefits for atherosclerosis prevention (CHIBA study)

被引:88
作者
Yokote, Koutaro [1 ]
Bujo, Hideaki [2 ]
Hanaoka, Hideki [3 ]
Shinomiya, Masaki [4 ]
Mikami, Keiji [5 ]
Miyashita, Yoh [6 ]
Nishikawa, Tetsuo [7 ]
Kodama, Tatsuhiko [8 ]
Tada, Norio [9 ]
Saito, Yasushi [1 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Clin Cell Biol & Med, Chiba, Japan
[2] Chiba Univ, Grad Sch Med, Dept Genome Res & Clin Applicat, Chiba, Japan
[3] Chiba Univ Hosp, Dept Clin Res, Chiba, Japan
[4] Nishifuma Naika, Chiba, Japan
[5] Omigawa Gen Hosp, Dept Internal Med, Chiba, Japan
[6] Toho Univ, Sch Med, Sakura Med Ctr, Dept Internal Med, Chiba 2748510, Japan
[7] Yokohama Rosai Hosp, Dept Med, Div Endocrinol & Metab, Kanagawa, Japan
[8] Univ Tokyo, Adv Sci & Technol Res Ctr, Lab Syst Biol & Med, Tokyo, Japan
[9] Jikei Univ, Kashiwa Hosp, Dept Internal Med, Div Gen Med, Chiba, Japan
关键词
Statins; Non-HDL-cholesterol; Obesity; Metabolic syndrome; Hepatic enzymes;
D O I
10.1016/j.atherosclerosis.2008.02.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: To compare the efficacy and safety of pitavastatin and atorvastatin in Japanese patients with hypercholesterolemia. Methods and results: Japanese patients with total cholesterol (TC) >= 220 mg/dL were randomized to receive pitavastatin 2 mg (n = 126) or atorvastatin 10 mg (n = 125) for 12 weeks. The primary endpoint was percent change front baseline in non-HDL-C level after 12 weeks of treatment. Reduction of non-HDL-C by pitavastatin treatment (39.0%, P = 0.456 vs. atorvastatin) was non-inferior to that by atorvastatin (40.3%). Both pitavastatin and atorvastatin also significantly reduced LDL-C by 42.6% and 44.1%, TC by 29.7% and 31.1% and TG by 17314 and 10.7%. respectively. at 12 weeks without intergroup differences. HDL-C showed a significant increase at 12 weeks with pitavastatin treatment (3.2%, P = 0.033 vs. baseline) but not with atorvastatin treatment ( 1.7%, P = 0.221 vs. baseline). Waist circumference. body weight and BMI were significantly correlated with percent reduction of non-HDL-C in the atorvastatin group, whereas pitavastatin showed consistent reduction of non-HDL-C regardless of the body size. fit patients with metabolic syndrome, LDL-C was reduced significantly more in patients receiving pitavastatin when compared with those receiving atorvastatin. AST. ALT and gamma GTP increased significantly in patients receiving atorvastatin but not in those receiving pitavastatin. Both treatments were well tolerated. Conclusion: Pitavastatin 2 mg, and atorvastatin 10 mg are equally effective in improving the lipid profile mid were well tolerated in Japanese patients with hypercholesterolemia. (C) 2008 Published by Elsevier Ireland Ltd.
引用
收藏
页码:345 / 352
页数:8
相关论文
共 28 条
[1]   The metabolic syndrome - a new worldwide definition [J].
Alberti, KGMM ;
Zimmet, P ;
Shaw, J .
LANCET, 2005, 366 (9491) :1059-1062
[2]   Effects of grapefruit juice on the pharmacokinetics of pitavastatin and atorvastatin [J].
Ando, H ;
Tsuruoka, S ;
Yanagihara, H ;
Sugimoto, K ;
Miyata, M ;
Yamazoe, Y ;
Takamura, T ;
Kaneko, S ;
Fujimura, A .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 60 (05) :494-497
[3]  
[Anonymous], 2005, Nihon Naika Gakkai Zasshi, V94, P794
[4]  
Bittner Vera, 2004, Prev Cardiol, V7, P122, DOI 10.1111/j.1520-037X.2004.3094.x
[5]   Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III) [J].
Cleeman, JI ;
Grundy, SM ;
Becker, D ;
Clark, LT ;
Cooper, RS ;
Denke, MA ;
Howard, WJ ;
Hunninghake, DB ;
Illingworth, DR ;
Luepker, RV ;
McBride, P ;
McKenney, JM ;
Pasternak, RC ;
Stone, NJ ;
Van Horn, L ;
Brewer, HB ;
Ernst, ND ;
Gordon, D ;
Levy, D ;
Rifkind, B ;
Rossouw, JE ;
Savage, P ;
Haffner, SM ;
Orloff, DG ;
Proschan, MA ;
Schwartz, JS ;
Sempos, CT ;
Shero, ST ;
Murray, EZ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19) :2486-2497
[6]   Primary prevention of cardiovascular disease with atorvastatin in type 2 diabetes in the Collaborative Atorvastatin Diabetes Study (CARDS): multicentre randomised placebo-controlled trial [J].
Colhoun, HM ;
Betteridge, DJ ;
Durrington, PN ;
Hitman, GA ;
Neil, HAW ;
Livingstone, SJ ;
Thomason, MJ ;
Mackness, MI ;
Charlton-Menys, V ;
Fuller, JH .
LANCET, 2004, 364 (9435) :685-696
[7]   Pitavastatin ameliorates severe hepatic steatosis in aromatase-deficient (Ar-/-) mice [J].
Egawa, T ;
Toda, K ;
Nemoto, Y ;
Ono, M ;
Akisawa, N ;
Saibara, T ;
Hayashi, Y ;
Hiroi, M ;
Enzan, H ;
Onishi, S .
LIPIDS, 2003, 38 (05) :519-523
[8]  
Fujino H, 2004, ARZNEIMITTEL-FORSCH, V54, P382
[9]  
Fujino H, 2002, ARZNEIMITTELFORSCH, V52, P745
[10]   Lipoprotein lipase (LPL) mass in preheparin serum reflects insulin sensitivity [J].
Hanyu, O ;
Miida, T ;
Obayashi, K ;
Ikarashi, T ;
Soda, S ;
Kaneko, S ;
Hirayama, S ;
Suzuki, K ;
Nakamura, Y ;
Yamatani, K ;
Aizawa, Y .
ATHEROSCLEROSIS, 2004, 174 (02) :385-390