Effects of adding fenofibrate (200 mg/day) to simvastatin (10 mg/day) in patients with combined Hyperlipidemia and metabolic syndrome

被引:124
作者
Vega, GL
Ma, PTS
Cater, NB
Filipchuk, N
Meguro, S
Garcia-Garcia, AB
Grundy, SM
机构
[1] Univ Texas, SW Med Ctr, Ctr Human Nutr, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Clin Nutr, Dallas, TX 75390 USA
[3] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX 75390 USA
[4] Vet Affairs Med Ctr, Dallas, TX USA
[5] Heart Hlth Inst, Calgary, AB, Canada
关键词
D O I
10.1016/S0002-9149(03)00111-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Combined hyperlipidemia predisposes subjects to coronary heart disease. Two lipid abnormalities-increased cholesterol and atherogenic dyslipidemia-are potential targets of lipid-lowering therapy. Successful management of both may require combined drug therapy. Statins are effective low-density lipoprotein (LDL) cholesterol-lowering drugs. For atherogenic dyslipidemia (high triglycerides, small LDL, and low high-density lipoprotein [HDL]), fibrates are potentially beneficial. The present study was designed to examine the safety and efficacy of a combination of low-dose simivastatin and fenofibrate in the treatment of combined hyperlipidemia. It was a randomized, placebo-controlled trial with a crossover design. Three randomized phases were employed (double placebo, simvastatin 10 mg/day and placebo, and simvastatin 10 mg/day plus fenofibrate 200 mg/day). Each phase lasted ' 3 months, and in the lost week. of each phase, measurements were made of plasma lipids, lipoprotein cholesterol, plasma apolipoproteins B, C-II, and C-III and LDL speciation on 3 consecutive days. Simivastatin therapy decreased total cholesterol by 27%, non-HDL cholesterol by 30%, total apolipoprotein B by 31%, very low-density lipoprotein (VLDL) + intermediate-density lipoprotein (IDL) cholesterol by 37%, VLDL + IDL apolipoprotein B by 14%, LDL cholesterol by 28%, and LDL apolipoprotein B by 21%. The addition of fenofibrate caused an additional decrease in VLDL + IDL cholesterol and VLDL + IDL apolipoprotein B by 36% and 32%, respectively. Simvastatin alone caused a small increase in the ratio of large-to-small LDL, whereas the addition of fenofibrate to simvastatin therapy caused a marked increase in the ratio of large-to-small LDL species. Simivastatin alone produced a small (6%) and insignificant increase in HDL cholesterol concentrations. When fenofibrate was added to simvastatin therapy, HDL cholesterol increased significantly by 23%. No significant side effects were observed with either simvastatin alone or with combined drug therapy. Therefore, a combination of simvastatin 10 mg/day and fenofibrate 200 mg/day appears to be effective and safe for the treatment of atherogenic dyslipidemia in combined hyperlipidemia. (C) 2003 by Excerpta Medica, Inc.
引用
收藏
页码:956 / 960
页数:5
相关论文
共 30 条
[1]  
[Anonymous], 1994, CIRCULATION
[2]   High-density lipoprotein cholesterol as a predictor of coronary heart disease risk. The PROCAM experience and pathophysiological implications for reverse cholesterol transport [J].
Assmann, G ;
Schulte, H ;
vonEckardstein, A ;
Huang, YD .
ATHEROSCLEROSIS, 1996, 124 :S11-S20
[3]   Cardiovascular disease mortality in familial forms of hypertriglyceridemia: A 20-year prospective study [J].
Austin, MA ;
McKnight, B ;
Edwards, KL ;
Bradley, CM ;
McNeely, MJ ;
Psaty, BM ;
Brunzell, JD ;
Motulsky, AC .
CIRCULATION, 2000, 101 (24) :2777-2782
[4]  
AUSTIN MA, 1988, JAMA-J AM MED ASSOC, V260, P1917
[5]  
Bachorik PS, 1997, CLIN CHEM, V43, P2364
[6]   15 YEAR MORTALITY IN CORONARY DRUG PROJECT PATIENTS - LONG-TERM BENEFIT WITH NIACIN [J].
CANNER, PL ;
BERGE, KG ;
WENGER, NK ;
STAMLER, J ;
FRIEDMAN, L ;
PRINEAS, RJ ;
FRIEDEWALD, W .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1986, 8 (06) :1245-1255
[7]  
CARLSON LA, 1988, ACTA MED SCAND, V223, P405
[8]   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
[9]   COMBINATION-DRUG THERAPY FOR FAMILIAL COMBINED HYPERLIPIDEMIA [J].
EAST, C ;
BILHEIMER, DW ;
GRUNDY, SM .
ANNALS OF INTERNAL MEDICINE, 1988, 109 (01) :25-32
[10]   Angiographic assessment of effects of bezafibrate on progression of coronary artery disease in young male postinfarction patients [J].
Ericsson, CG ;
Hamsten, A ;
Nilsson, J ;
Grip, L ;
Svane, B ;
deFaire, U .
LANCET, 1996, 347 (9005) :849-853