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Blunted fat oxidation upon submaximal exercise is partially compensated by enhanced glucose metabolism in children, adolescents, and young adults with Barth syndrome.

Citation
Cade, W. T., et al. “Blunted Fat Oxidation Upon Submaximal Exercise Is Partially Compensated By Enhanced Glucose Metabolism In Children, Adolescents, And Young Adults With Barth Syndrome.”. Journal Of Inherited Metabolic Disease, pp. 480-493.
Center Washington University in St Louis
Author William Todd Cade, Kathryn L Bohnert, Linda R Peterson, Bruce W Patterson, Adam J Bittel, Adewole L Okunade, Lisa de Las Fuentes, Karen Steger-May, Adil Bashir, George G Schweitzer, Shaji K Chacko, Ronald J Wanders, Christina A Pacak, Barry J Byrne, Dominic N Reeds
Keywords Barth syndrome, Exercise, fatty acid, mitochondria
Abstract

Barth syndrome (BTHS) is a rare X-linked condition resulting in abnormal mitochondria, cardioskeletal myopathy, and growth delay; however, the effects of BTHS on substrate metabolism regulation and their relationships with tissue function in humans are unknown. We sought to characterize glucose and fat metabolism during rest, submaximal exercise, and postexercise rest in children, adolescents, and young adults with BTHS and unaffected controls and examine their relationships with cardioskeletal energetics and function. Children/adolescents and young adults with BTHS (n = 29) and children/adolescent and young adult control participants (n = 28, total n = 57) underwent an infusion of 6'6'H2 glucose and U- C palmitate and indirect calorimetry during rest, 30-minutes of moderate exercise (50% ), and recovery. Cardiac function, cardioskeletal mitochondrial energetics, and exercise capacity were examined via echocardiography, P magnetic resonance spectroscopy, and peak exercise testing, respectively. The glucose turnover rate was significantly higher in individuals with BTHS during rest (33.2 ± 9.8 vs 27.2 ± 8.1 μmol/kgFFM/min, P < .01) and exercise (34.7 ± 11.2 vs 29.5 ± 8.8 μmol/kgFFM/min, P < .05) and tended to be higher postexercise (33.7 ± 10.2 vs 28.8 ± 8.0 μmol/kgFFM/min, P < .06) compared to controls. Increases in total fat (-3.9 ± 7.5 vs 10.5 ± 8.4 μmol/kgFFM/min, P < .0001) and plasma fatty acid oxidation rates (0.0 ± 1.8 vs 5.1 ± 3.9 μmol/kgFFM/min, P < .0001) from rest to exercise were severely blunted in BTHS compared to controls. Conclusion: An inability to upregulate fat metabolism during moderate intensity exercise appears to be partially compensated by elevations in glucose metabolism. Derangements in fat and glucose metabolism are characteristic of the pathophysiology of BTHS. A severely blunted ability to upregulate fat metabolism during a modest level of physical activity is a defining pathophysiologic characteristic in children, adolescents, and young adults with BTHS.

Year of Publication
2019
Journal
Journal of inherited metabolic disease
Volume
42
Issue
3
Number of Pages
480-493
Date Published
12/2019
ISSN Number
1573-2665
DOI
10.1002/jimd.12094
Alternate Journal
J. Inherit. Metab. Dis.
PMID
30924938
PMCID
PMC6483838
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