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Impact of pioglitazone on coronary endothelial function in non-diabetic patients with coronary artery disease
Jochen Wöhrle1, Nikolaus Marx, Wolfgang Koenig
1Department of Internal Medicine II, University of Ulm, Ulm, Germany. jochen.woehrle@uniklinik-ulm.de
Insights
Pioglitazone significantly improved coronary endothelial function in non-diabetic patients with coronary artery disease (CAD). This study found pioglitazone enhanced blood vessel response compared to placebo.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Pioglitazone demonstrates antiatherosclerotic effects beyond glycemic control.
- Coronary artery disease (CAD) involves endothelial dysfunction.
Purpose of the Study:
- To investigate if pioglitazone improves coronary endothelial dysfunction in non-diabetic CAD patients.
- To assess pioglitazone's effects in a randomized, placebo-controlled trial.
Main Methods:
- 50 non-diabetic CAD patients received pioglitazone or placebo for 6 months.
- Coronary endothelial function assessed via intracoronary infusions (adenosine, acetylcholine, glyceroltrinitrate) and cold pressor test (CPT).
- Primary endpoint: acetylcholine-induced coronary vascular response measured by quantitative coronary angiography.
Main Results:
- No baseline differences in endothelial function.
- Pioglitazone group showed a 1.8% increase in luminal area; placebo group showed a 7.6% decrease (P < 0.008).
- A trend for improved CPT response in the pioglitazone group (P = 0.057).
Conclusions:
- Pioglitazone treatment significantly improved coronary endothelial function in non-diabetic patients with CAD.
- Results suggest pioglitazone has direct vascular benefits in CAD.
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 microg/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.
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