Effect of micronized fenofibrate on plasma lipoprotein levels and hemostatic parameters of hypertriglyceridemic patients with low levels of high-density lipoprotein cholesterol in the fed and fasted state

被引:49
作者
Genest, J
Nguyen, NH
Theroux, P
Davignon, J
Cohn, JS
机构
[1] Clin Res Inst Montreal, Cardiovasc Genet Lab, Montreal, PQ H2W 1R7, Canada
[2] Clin Res Inst Montreal, Hyperlipidemia & Atherosclerosis Res Grp, Montreal, PQ H2W 1R7, Canada
[3] CHUM, Cardiol Serv & Lipid Clin, Montreal, PQ, Canada
[4] Montreal Heart Inst, Montreal, PQ H1T 1C8, Canada
关键词
fenofibrate; micronized; hypertriglyceridemia; HDL; postprandial;
D O I
10.1097/00005344-200001000-00022
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A randomized, double-blind, placebo-controlled study was undertaken in 20 hypertriglyceridemic men [plasma triglyceride (TG), >2.3 mM] with low levels (<0.9 mM) of high-density lipoprotein cholesterol (HDL-C) to investigate the ability of micronized fenofibrate (Tricor or Lipidil; 200 mg/ day) to affect atherogenic and thrombogenic plasma risk factors in the fed and fasted state. Each patient underwent (a) 4 weeks of dietary stabilization, (b) 8 weeks of treatment with fenofibrate or placebo, (c) a 5-week washout period, and (d) 8-weeks of treatment with the alternative medication. An oral fat-loading test (1 g fat/kg body weight) was carried out after both treatment periods. Before treatment, patients had a mean (+/-SD) total plasma TG of 3.31 +/- 0.93 mM; total C, 5.75 +/- 0.89 mM; HDL-C, 0.71 +/- 0.09 mM; and low-density lipoprotein (LDL)C, 3.40 +/- 0.68 mM. Compared with placebo, fenofibrate reduced fasting TG levels by 36%, and triglyceride-rich lipoprotein (TRL, d < 1.006 g/ml) -TG, and TRL-C levels by similar to 40%. In the postprandial state, fenofibrate reduced total TG, TRL-TG, TRL-C, TRL-apoC-III, and TRL-apoE levels by similar to 35% (all values of p < 0.01). Fasted and fed HDL-C and apoA-I levels were increased similar to 10%, and total cholesterol/HDL cholesterol ratios were decreased similar to 15% by fenofibrate. No significant differences were observed in mean LDL-C and LDL-apoB levels. A 6% increase in the LDL-C/LDL-apoB ratio during fenofibrate treatment indicated a shift to larger, more buoyant LDL par tides. A small, but statistically significant (p < 0.01) increase was observed in fasted and fed Lp(a) levels during fenofibrate treatment. Hemostatic parameters were not significantly affected by fenofibrate, except for a 12-15% decrease (p < 0.05) in fibrinogen levels in the fasted and fed state, and a significant increase (43%; p < 0.05) in fasting levels of plasminogen activator-inhibitor-1. These data demonstrate that micronized fenofibrate is highly effective, in both the fed and fasted state, in reducing TRL lipids and apolipoproteins, and in reducing plasma fibrinogen levels of men with an atherogenic lipoprotein profile.
引用
收藏
页码:164 / 172
页数:9
相关论文
共 34 条
[1]   Micronised fenofibrate - Review of its pharmacodynamic properties and clinical efficacy in the management of dyslipidaemia [J].
Adkins, JC ;
Faulds, D .
DRUGS, 1997, 54 (04) :615-633
[2]   Studies on the mechanism of fibrate-inhibited expression of plasminogen activator inhibitor-1 in cultured hepatocytes from cynomolgus monkey [J].
Arts, J ;
Kockx, M ;
Princen, HMG ;
Kooistra, T .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (01) :26-32
[3]   FENOFIBRATE - A REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES AND THERAPEUTIC USE IN DYSLIPIDEMIA [J].
BALFOUR, JA ;
MCTAVISH, D ;
HEEL, RC .
DRUGS, 1990, 40 (02) :260-290
[4]  
Cohn Jeffrey S., 1994, Current Opinion in Lipidology, V5, P185
[5]  
Cohn JS, 1998, CAN J CARDIOL, V14, p18B
[6]   Plasma concentration of apolipoprotein E in intermediate-sized remnant-like lipoproteins in normolipidemic and hyperlipidemic subjects [J].
Cohn, JS ;
Tremblay, M ;
Amiot, M ;
Bouthillier, D ;
Roy, M ;
Genest, J ;
Davignon, J .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1996, 16 (01) :149-159
[7]   Effects of two different fibric acid derivatives on lipoproteins, cholesteryl ester transfer, fibrinogen, plasminogen activator inhibitor and paraoxonase activity in type IIb hyperlipoproteinaemia [J].
Durrington, PN ;
Mackness, MI ;
Bhatnagar, D ;
Julier, K ;
Prais, H ;
Arrol, S ;
Morgan, J ;
Wood, GNI .
ATHEROSCLEROSIS, 1998, 138 (01) :217-225
[8]   FIBRINOGEN AS A CARDIOVASCULAR RISK FACTOR - A METAANALYSIS AND REVIEW OF THE LITERATURE [J].
ERNST, E ;
RESCH, KL .
ANNALS OF INTERNAL MEDICINE, 1993, 118 (12) :956-963
[9]   COMPARATIVE EFFICACY AND SAFETY OF MICRONIZED FENOFIBRATE AND SIMVASTATIN IN PATIENTS WITH PRIMARY TYPE IIA OR IIB HYPERLIPIDEMIA [J].
FARNIER, M ;
BONNEFOUS, F ;
DEBBAS, N ;
IRVINE, A .
ARCHIVES OF INTERNAL MEDICINE, 1994, 154 (04) :441-449
[10]  
FOGER B, 1994, CLIN INVESTIGATOR, V72, P294