Journal
CARDIOVASCULAR THERAPEUTICS
Volume 31, Issue 3, Pages 161-167Publisher
WILEY-BLACKWELL
DOI: 10.1111/j.1755-5922.2011.00307.x
Keywords
Coronary flow velocity reserve; Endothelial function; Homocysteine; PPAR-alpha
Funding
- Major National Basic Research Program of P. R. China [2011CB503904]
- Chinese National Natural Science Foundation [30730042, 30821001, 81070701, 30770873, 81070244]
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Introduction: Fenofibrate, an agonist of peroxisome proliferator-activated receptor- (PPAR-), has a vascular protective effect. Aims: We investigated the effect of the PPAR- agonist on coronary artery endothelial function in patients with hypertriglyceridemia. Methods: Fifty-eight patients with hypertriglyceridemia were divided into two groups: control (no treatment; n = 23) and fenofibrate treatment (n = 35), 200 mg/d, for 6 months. The patients had undergone rest and adenosine treatment to induce hyperemia for quantification of coronary flow velocity reserve (CFVR) by noninvasive Doppler echocardiography before treatment and at 6-month follow-up. Pulse wave velocity (PWV) was measured before treatment and at 6-month follow-up. Results: CFVR was significantly improved with fenofibrate treatment as compared with baseline level and control group (3.14 +/- 0.36 vs. 2.80 +/- 0.58 and 2.79 +/- 0.65, P < 0.01 and 0.05, respectively), with no difference between baseline levels and untreated controls. In addition, at 6 months, plasma level of homocysteine was significantly increased with fenofibrate treatment as compared with at baseline and control group (median 18.13 [range 14.4622.02]mol/L vs. 14.09 [12.0118.81] and 13.34 [9.6917.06]mol/L, P < 0.001 and 0.01, respectively). Furthermore, at 6 months, PWV was significantly decreased with fenofibrate treatment as compared with control group (1446 +/- 136 cm/s vs. 1570 +/- 203 cm/s, P < 0.05). Conclusions: Treatment with PPAR- agonist fenofibrate significantly improved CFVR and arterial stiffness in patients with hypertriglyceridemia. This endothelial protective effect may be reduced in part by the side effect of increasing homocysteine.
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