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

Using a novel positron emission tomography (PET) method with oral administration of 14( R, S)-[ 18 F]-fluoro-6-thia-heptadecanoic acid ( 18 FTHA), we recently demonstrated that subjects with impaired glucose tolerance (IGT) display an impairment in cardiac function associated with increased myocardi...

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Published inAmerican journal of physiology: endocrinology and metabolism Vol. 306; no. 12; pp. E1388 - E1396
Main Authors Labbé, Sébastien M., Noll, Christophe, Grenier-Larouche, Thomas, Kunach, Margaret, Bouffard, Lucie, Phoenix, Serge, Guérin, Brigitte, Baillargeon, Jean-Patrice, Langlois, Marie-France, Turcotte, Eric E., Carpentier, André C.
Format Journal Article
LanguageEnglish
Published United States American Physiological Society 15.06.2014
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Online AccessGet full text
ISSN0193-1849
1522-1555
1522-1555
DOI10.1152/ajpendo.00638.2013

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Abstract Using a novel positron emission tomography (PET) method with oral administration of 14( R, S)-[ 18 F]-fluoro-6-thia-heptadecanoic acid ( 18 FTHA), 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 18 FTHA method, and cardiac function and oxidative metabolic index using PET [ 11 C]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.
AbstractList 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.
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.
Using a novel positron emission tomography (PET) method with oral administration of 14( R, S)-[ 18 F]-fluoro-6-thia-heptadecanoic acid ( 18 FTHA), 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 18 FTHA method, and cardiac function and oxidative metabolic index using PET [ 11 C]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.
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.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.
Author Guérin, Brigitte
Langlois, Marie-France
Carpentier, André C.
Kunach, Margaret
Noll, Christophe
Grenier-Larouche, Thomas
Turcotte, Eric E.
Baillargeon, Jean-Patrice
Labbé, Sébastien M.
Bouffard, Lucie
Phoenix, Serge
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Cites_doi 10.1089/met.2008.0063
10.1007/s10554-012-0174-6
10.1016/j.jacc.2009.07.054
10.2337/db10-0997
10.1093/cvr/cvr212
10.1152/ajpendo.00416.2010
10.1152/ajpendo.00557.2004
10.1161/CIRCRESAHA.107.160457
10.2337/db11-1805
10.2337/diabetes.48.6.1245
10.1038/jcbfm.1985.87
10.2337/dc13-1423
10.1016/j.amjcard.2009.02.025
10.1007/s11307-006-0042-7
10.1007/s00259-010-1443-z
10.1152/ajpendo.00579.2010
10.1080/07315724.1999.10718853
10.1152/ajpendo.00560.2009
10.2337/diabetes.52.3.614
10.1152/ajpendo.00233.2005
10.1210/jc.2012-1219
10.1136/heartjnl-2012-301778
10.1007/s001250051597
10.2337/db06-1552
10.1016/j.yjmcc.2007.08.020
10.1161/CIRCULATIONAHA.108.803916
10.2217/clp.11.60
10.1161/CIRCULATIONAHA.106.679597
10.1056/NEJMoa012512
10.1002/oby.20027
10.1074/jbc.M109.049817
10.1186/1475-2840-10-47
10.1210/jc.2006-0584
10.1093/ajcn/88.4.1134
10.2337/db06-0822
10.1172/JCI60433
10.1210/jc.2007-1670
10.1371/journal.pone.0010956
10.1007/s002590000472
10.1007/s10554-013-0302-y
10.1016/j.diabet.2011.01.003
10.1007/s00125-008-1040-x
10.1161/CIRCULATIONAHA.106.645614
10.1186/1475-2840-8-39
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  doi: 10.1089/met.2008.0063
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  doi: 10.1007/s10554-012-0174-6
– volume: 42
  start-page: 1174
  year: 2001
  ident: B42
  publication-title: J Nucl Med
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  doi: 10.1016/j.jacc.2009.07.054
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  doi: 10.2337/db10-0997
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  doi: 10.1093/cvr/cvr212
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  doi: 10.1152/ajpendo.00416.2010
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  doi: 10.1152/ajpendo.00557.2004
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  doi: 10.1161/CIRCRESAHA.107.160457
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  doi: 10.2337/db11-1805
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  doi: 10.2337/diabetes.48.6.1245
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  doi: 10.1038/jcbfm.1985.87
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  doi: 10.1007/s00259-010-1443-z
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  doi: 10.1152/ajpendo.00579.2010
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  doi: 10.1080/07315724.1999.10718853
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  doi: 10.1152/ajpendo.00560.2009
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  doi: 10.2337/diabetes.52.3.614
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  doi: 10.1152/ajpendo.00233.2005
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  doi: 10.1210/jc.2012-1219
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  doi: 10.1136/heartjnl-2012-301778
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  doi: 10.1007/s001250051597
– ident: B28
  doi: 10.2337/db06-1552
– ident: B44
  publication-title: Clin Endocrinol
– ident: B1
  doi: 10.1016/j.yjmcc.2007.08.020
– ident: B43
  doi: 10.1161/CIRCULATIONAHA.108.803916
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  doi: 10.2217/clp.11.60
– volume: 47
  start-page: 689
  year: 2006
  ident: B47
  publication-title: J Nucl Med
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  doi: 10.1161/CIRCULATIONAHA.106.679597
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  doi: 10.1056/NEJMoa012512
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  doi: 10.1002/oby.20027
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  doi: 10.1074/jbc.M109.049817
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  doi: 10.1186/1475-2840-10-47
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  doi: 10.1210/jc.2006-0584
– ident: B35
  doi: 10.1093/ajcn/88.4.1134
– ident: B2
  doi: 10.2337/db06-0822
– ident: B31
  doi: 10.1172/JCI60433
– ident: B5
  doi: 10.1210/jc.2007-1670
– ident: B29
  doi: 10.1371/journal.pone.0010956
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  doi: 10.1007/s002590000472
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  doi: 10.1007/s10554-013-0302-y
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  doi: 10.1016/j.diabet.2011.01.003
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  doi: 10.1007/s00125-008-1040-x
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  doi: 10.1161/CIRCULATIONAHA.106.645614
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Snippet Using a novel positron emission tomography (PET) method with oral administration of 14( R, S)-[ 18 F]-fluoro-6-thia-heptadecanoic acid ( 18 FTHA), we recently...
Using a novel positron emission tomography (PET) method with oral administration of 14(R,S)-[¹⁸F]-fluoro-6-thia-heptadecanoic acid (¹⁸FTHA), we recently...
Using a novel positron emission tomography (PET) method with oral administration of 14(R,S)-[18F]-fluoro-6-thia-heptadecanoic acid (18FTHA), we recently...
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SubjectTerms Acetic Acid
Body Mass Index
Carbon Radioisotopes
Combined Modality Therapy
Diet, Reducing
Dietary Fats - metabolism
Fatty Acids
Female
Fluorine Radioisotopes
Glucose
Glucose Intolerance - etiology
Glucose Intolerance - prevention & control
Heart Ventricles - diagnostic imaging
Heart Ventricles - metabolism
Heart Ventricles - physiopathology
Humans
Insulin
Intervention
Life Style
Male
Middle Aged
Motor Activity
Obesity - diet therapy
Obesity - metabolism
Obesity - physiopathology
Obesity - therapy
Positron-Emission Tomography
Postprandial Period
Radionuclide Ventriculography
Radiopharmaceuticals
Tomography
Ventricular Dysfunction, Left - diagnostic imaging
Ventricular Dysfunction, Left - etiology
Ventricular Dysfunction, Left - prevention & control
Weight Loss
Title Improved cardiac function and dietary fatty acid metabolism after modest weight loss in subjects with impaired glucose tolerance
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