Improved cardiac function and dietary fatty acid metabolism after modest weight loss in subjects with impaired glucose tolerance

Sébastien M. Labbé(Université de Sherbrooke), Christophe Noll(Université de Sherbrooke), Thomas Grenier–Larouche(Université de Sherbrooke), Margaret Kunach(Université de Sherbrooke), Lucie Bouffard(Université de Sherbrooke), Serge Phoenix(Université de Sherbrooke), Brigitte Guérin(Université de Sherbrooke), Jean‐Patrice Baillargeon(Université de Sherbrooke), Marie‐France Langlois(Université de Sherbrooke), Éric Turcotte(Université de Sherbrooke), André C. Carpentier(Université de Sherbrooke)
American Journal of Physiology-Endocrinology and Metabolism
April 23, 2014
Cited by 28

Abstract

Using a novel positron emission tomography (PET) method with oral administration of 14(R,S)-[¹⁸F]-fluoro-6-thia-heptadecanoic acid (¹⁸FTHA), we recently demonstrated that subjects with impaired glucose tolerance (IGT) display an impairment in cardiac function associated with increased myocardial uptake of dietary fatty acids. Here, we determined whether modest weight loss induced by lifestyle changes might improve these cardiac metabolic and functional abnormalities. Nine participants with IGT, enrolled in a one-year lifestyle intervention trial, were invited to undergo determination of organ-specific postprandial dietary fatty acids partition using the oral ¹⁸FTHA method, and cardiac function and oxidative metabolic index using PET [¹¹C]acetate kinetics with ECG-gated PET ventriculography before and after the intervention. The intervention resulted in significant weight loss and reduction of waist circumference, with reduced postprandial plasma glucose, insulin, and triglycerides excursion. We observed a significant increase in stroke volume, cardiac output, and left ventricular ejection fraction associated with reduced myocardial oxidative metabolic index and fractional dietary fatty acid uptake. Modest weight loss corrects the exaggerated myocardial channeling of dietary fatty acids and improves myocardial energy substrate metabolism and function in IGT subjects.


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