Effects of fenofibrate on lipoproteins, vasomotor function, and serological markers of inflammation, plaque stabilization, and hemostasis

被引:60
作者
Koh, KK
Ahn, JY
Han, SH
Jin, DK
Kim, HS
Lee, KC
Shin, EK
Sakuma, I
机构
[1] Gachon Med Sch, Gil Heart Ctr, Dept Cardiol, Vasc Med & Atherosclerosis Unit, Inchon 405760, South Korea
[2] Gachon Med Sch, Dept Clin Pathol, Inchon 405760, South Korea
[3] Gachon Med Sch, Dept Radiol, Inchon 405760, South Korea
[4] Gachon Med Sch, Dept Anesthesiol & Pain Med, Inchon 405760, South Korea
[5] Hokkaido Univ, Grad Sch Med, Dept Cardiovasc Med, Sapporo, Hokkaido, Japan
关键词
fibrate; hyperlipidemia; endothelial function; atherosclerosis;
D O I
10.1016/j.atherosclerosis.2004.01.033
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We investigated the effects of fenofibrate, peroxisome proliferator-activated receptors (PPARs) agonist, on endothelial function in patients with hypertriglyceridemia. We administered placebo or fenofibrate 200 mg daily to 25 patients with hypertriglyceridemia for 8 weeks. This study was randomized, double-blind, placebo-controlled, crossover in design. Compared with placebo, fenofibrate significantly changed lipoprotein levels including non-HDL cholesterol and significantly improved the percent flow-mediated dilator response to hyperemia by 33 +/- 6% (P < 0.001) and lowered plasma levels of tumor necrosis factor-alpha by 13 +/- 3% (P = 0.002). Fenofibrate reduced fibrinogen and plasminogen activator inhibitor type 1 antigen levels by 17 +/- 3 and 10 +/- 3%, respectively (P < 0.001 and P = 0.014, respectively). However, fenofibrate did not significantly change plasma levels of nitrate, malondialdehyde, tissue factor activity, and serological markers of plaque stabilization. Fenofibrate significantly changed lipoprotein levels and improved the percent flow-mediated dilator response to hyperemia as well as lowered levels of tumor necrosis factor-alpha (TNF-alpha), fibrinogen, and plasminogen activator inhibitor type 1 antigen. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:379 / 383
页数:5
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