Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/17528
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Type: Journal article
Title: Metabolic modulation with perhexiline in chronic heart failure - a randomized, controlled trial of short-term use of a novel treatment
Author: Lee, L.
Campbell, R.
Scheuermann-Freestone, M.
Taylor, R.
Gunaruwan, P.
Williams, L.
Ashrafian, H.
Horowitz, J.
Fraser, A.
Clarke, K.
Frenneaux, M.
Citation: Circulation, 2005; 112(21):3280-3288
Publisher: Lippincott Williams & Wilkins
Issue Date: 2005
ISSN: 0009-7322
1524-4539
Statement of
Responsibility: 
Leong Lee, Ross Campbell, Michaela Scheuermann-Freestone, Rachel Taylor, Prasad Gunaruwan, Lynne Williams, Houman Ashrafian, John Horowitz, Alan G. Fraser, Kieran Clarke, and Michael Frenneaux
Abstract: Chronic heart failure (CHF) is a major cause of morbidity and mortality that requires a novel approach to therapy. Perhexiline is an antianginal drug that augments glucose metabolism by blocking muscle mitochondrial free fatty acid uptake, thereby increasing metabolic efficiency. We assessed the effects of perhexiline treatment in CHF patients.In a double-blind fashion, we randomly assigned patients with optimally medicated CHF to either perhexiline (n=28) or placebo (n=28). The primary end point was peak exercise oxygen consumption (VO2max), an important prognostic marker. In addition, the effect of perhexiline on myocardial function and quality of life was assessed. Quantitative stress echocardiography with tissue Doppler measurements was used to assess regional myocardial function in patients with ischemic CHF. 31P magnetic resonance spectroscopy was used to assess the effect of perhexiline on skeletal muscle energetics in patients with nonischemic CHF. Treatment with perhexiline led to significant improvements in VO2max (16.1+/-0.6 to 18.8+/-1.1 mL . kg(-1) . min(-1); P<0.001), quality of life (Minnesota score reduction from 45+/-5 to 34+/-5; P=0.04), and left ventricular ejection fraction (24+/-1% to 34+/-2%; P<0.001). Perhexiline treatment also increased resting and peak dobutamine stress regional myocardial function (by 15% and 24%, respectively) and normalized skeletal muscle phosphocreatine recovery after exercise. There were no adverse effects during the treatment period.In patients with CHF, metabolic modulation with perhexiline improved VO2max, left ventricular ejection fraction, symptoms, resting and peak stress myocardial function, and skeletal muscle energetics. Perhexiline may therefore represent a novel treatment for CHF with a good safety profile, provided that the dosage is adjusted according to plasma levels.
Keywords: Heart failure; metabolism; exercise; fatty acids; glucose
Description: Copyright © 2007 Lippincott Williams & Wilkins
RMID: 0020051384
DOI: 10.1161/CIRCULATIONAHA.105.551457
Appears in Collections:Medicine publications

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