Objective
Pioglitazone has been shown to exert multiple antiatherosclerotic actions independent from its glycemic effects. We studied
the hypothesis that pioglitazone improves coronary endothelial dysfunction in non-diabetic patients with coronary artery disease
(CAD) in a randomized, placebo-controlled, double-blind trial.
Methods
Fifty non-diabetic patients with CAD were randomized to 6 months treatment with pioglitazone 30 mg daily or placebo. Coronary
endothelial function was tested at baseline and after 6 months with intracoronary infusion of adenosine, acetylcholine (0.072;
0.72; 7.2, and 36 µg/min), glyceroltrinitrate, and cold pressor test (CPT). The primary endpoint was the mean effect of treatment
compared with placebo on acetylcholine-induced coronary vascular response for all acetylcholine dosages, based on percent
change in luminal area measured by quantitative coronary angiography.
Results
There was no difference in baseline coronary endothelial function. The primary endpoint was significantly different between
the groups with a 1.8% ± 2.0% increase in luminal area between baseline and follow-up with pioglitazone and a 7.6% ± 2.4%
decrease in the placebo group (P < 0.008). At follow-up, there was a trend for a difference in CPT (P = 0.057). No difference was observed regarding intracoronary glyceroltrinitrate or adenosine.
Conclusions
Pioglitazone treatment in non-diabetic patients with CAD was associated with a significantly better coronary endothelial function
compared to placebo.
Keywords acetylcholine - adenosine - endothelial function - coronary artery disease - PPAR