Effect of policosanol on lipid levels among patients with hypercholesterolemia or combined hyperlipidemia - A randomized controlled trial

被引:121
作者
Berthold, HK
Unverdorben, S
Degenhardt, R
Bulitta, M
Gouni-Berthold, I
机构
[1] Ctr Cardiovasc Dis, Inst Clin Res, Dept Clin Pharmacol, Rotenburg, Germany
[2] Clin Res Management Pharmaberatung GmbH, Rheinbach, Germany
[3] Univ Cologne, Dept Internal Med 2, Cologne, Germany
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2006年 / 295卷 / 19期
关键词
D O I
10.1001/jama.295.19.2262
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Policosanol is a natural substance derived from sugar cane that is advertised for its lipid-lowering effects as a nonprescription drug. More than 80 placebo-controlled or comparative trials, performed mostly by a single research institute, suggest that policosanol at doses of 5 to 40 mg/d has lipoprotein-lowering effects comparable with statins. Objectives To determine the lipoprotein-lowering effects of Cuban sugar cane derived policosanol and to establish, if effective, dose-dependency up to 80 mg/d in patients with hypercholesterolemia or combined hyperlipidemia. Design, Setting, and Participants A multicenter ( lipid outpatient clinics and general practitioners in Germany), randomized, double-blind, placebo-controlled, parallel-group trial conducted from September 29, 2000, to May 10, 2001, of patients with hypercholesterolemia or combined hyperlipidemia having baseline low-density lipoprotein cholesterol (LDL-C) levels of at least 150 mg/dL (>= 3.88 mmol/L) and either no or 1 cardiovascular risk factor other than known coronary heart disease, or baseline LDL-C levels of between 150 and 189 mg/dL (3.88-4.89 mmol/L) and 2 or more risk factors. Interventions Open-label 6-week placebo and diet run-in phase followed by a double-blind 12-week treatment phase after randomization to 5 groups: 10, 20, 40, or 80 mg/d of policosanol or placebo. Main Outcome Measure The percentage change of LDL-C, with changes in other lipoproteins as secondary outcome measures. Results A total of 143 patients were randomized to 5 equal groups and were analyzed on an intention-to-treat basis. In none of the 5 treatment groups did LDL-C levels decrease more than 10% from baseline. No statistically significant difference between policosanol and placebo was observed. A nonparametric test analyzing dose-dependency yielded nonsignificant results. In none of the secondary outcome measures, namely total cholesterol, high-density lipoprotein cholesterol (HDL-C), very low-density lipoprotein cholesterol, triglycerides, lipoprotein( a), and ratio of total or LDL-C to HDL-C, were there any significant effects of policosanol. Policosanol was tolerated well without serious adverse events. Conclusion In patients with hypercholesterolemia or combined hyperlipidemia, the sugar cane - derived policosanol in usual and high doses does not demonstrate a reduction in lipid levels beyond placebo.
引用
收藏
页码:2262 / 2269
页数:8
相关论文
共 33 条
[1]   Simple scoring scheme for calculating the risk of acute coronary events based on the 10-year follow-up of the Prospective Cardiovascular Munster (PROCAM) study [J].
Assmann, G ;
Cullen, P ;
Schulte, H .
CIRCULATION, 2002, 105 (03) :310-315
[2]  
AUFENANGER J, 1989, J CLIN CHEM CLIN BIO, V27, P807
[3]  
Batista J, 1996, INT J CLIN PHARM TH, V34, P134
[4]  
Castaño G, 2002, INT J CLIN PHARM RES, V22, P89
[5]  
Castaño G, 1999, INT J CLIN PHARM RES, V19, P105
[6]   Comparison of the efficacy and tolerability of policosanol with atorvastatin in elderly patients with type II hypercholesterolaemia [J].
Castaño, G ;
Mas, R ;
Fernández, L ;
Illnait, J ;
Mesa, M ;
Alvarez, E ;
Lezcay, M .
DRUGS & AGING, 2003, 20 (02) :153-163
[7]   Effects of policosanol and lovastatin in patients with intermittent claudication:: A double-blind comparative pilot study [J].
Castaño, G ;
Más, R ;
Fernández, L ;
Gámez, R ;
Illnait, J .
ANGIOLOGY, 2003, 54 (01) :25-38
[8]   Meta-analysis of natural therapies for hyperlipidemia: Plant sterols and stanols versus policosanol [J].
Chen, JT ;
Wesley, R ;
Shamburek, RD ;
Pucino, F ;
Csako, G .
PHARMACOTHERAPY, 2005, 25 (02) :171-183
[9]   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
[10]  
Crespo N, 1999, INT J CLIN PHARM RES, V19, P117