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Effects of fasting, feeding and exercise on plasma acylcarnitines among subjects with CPT2D, VLCADD and LCHADD/TFPD.

Authors :
Elizondo G
Matern D
Vockley J
Harding CO
Gillingham MB
Source :
Molecular genetics and metabolism [Mol Genet Metab] 2020 Sep - Oct; Vol. 131 (1-2), pp. 90-97. Date of Electronic Publication: 2020 Sep 06.
Publication Year :
2020

Abstract

Background: The plasma acylcarnitine profile is frequently used as a biochemical assessment for follow-up in diagnosed patients with fatty acid oxidation disorders (FAODs). Disease specific acylcarnitine species are elevated during metabolic decompensation but there is clinical and biochemical heterogeneity among patients and limited data on the utility of an acylcarnitine profile for routine clinical monitoring.<br />Methods: We evaluated plasma acylcarnitine profiles from 30 diagnosed patients with long-chain FAODs (carnitine palmitoyltransferase-2 (CPT2), very long-chain acyl-CoA dehydrogenase (VLCAD), and long-chain 3-hydroxy acyl-CoA dehydrogenase or mitochondrial trifunctional protein (LCHAD/TFP) deficiencies) collected after an overnight fast, after feeding a controlled low-fat diet, and before and after moderate exercise. Our purpose was to describe the variability in this biomarker and how various physiologic states effect the acylcarnitine concentrations in circulation.<br />Results: Disease specific acylcarnitine species were higher after an overnight fast and decreased by approximately 60% two hours after a controlled breakfast meal. Moderate-intensity exercise increased the acylcarnitine species but it varied by diagnosis. When analyzed for a genotype/phenotype correlation, the presence of the common LCHADD mutation (c.1528G > C) was associated with higher levels of 3-hydroxyacylcarnitines than in patients with other mutations.<br />Conclusions: We found that feeding consistently suppressed and that moderate intensity exercise increased disease specific acylcarnitine species, but the response to exercise was highly variable across subjects and diagnoses. The clinical utility of routine plasma acylcarnitine analysis for outpatient treatment monitoring remains questionable; however, if acylcarnitine profiles are measured in the clinical setting, standardized procedures are required for sample collection to be of value.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)

Subjects

Subjects :
3-Hydroxyacyl CoA Dehydrogenases genetics
3-Hydroxyacyl CoA Dehydrogenases metabolism
Acetyl-CoA C-Acyltransferase genetics
Acetyl-CoA C-Acyltransferase metabolism
Acyl-CoA Dehydrogenase, Long-Chain blood
Carbon-Carbon Double Bond Isomerases genetics
Carbon-Carbon Double Bond Isomerases metabolism
Cardiomyopathies diet therapy
Cardiomyopathies pathology
Cardiomyopathies therapy
Carnitine blood
Carnitine genetics
Carnitine metabolism
Carnitine O-Palmitoyltransferase blood
Congenital Bone Marrow Failure Syndromes diet therapy
Congenital Bone Marrow Failure Syndromes pathology
Congenital Bone Marrow Failure Syndromes therapy
Enoyl-CoA Hydratase genetics
Enoyl-CoA Hydratase metabolism
Exercise Therapy
Fasting
Female
Humans
Lipid Metabolism, Inborn Errors diet therapy
Lipid Metabolism, Inborn Errors pathology
Lipid Metabolism, Inborn Errors therapy
Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase blood
Male
Metabolism, Inborn Errors diet therapy
Metabolism, Inborn Errors pathology
Metabolism, Inborn Errors therapy
Mitochondrial Diseases diet therapy
Mitochondrial Diseases pathology
Mitochondrial Diseases therapy
Mitochondrial Myopathies diet therapy
Mitochondrial Myopathies pathology
Mitochondrial Myopathies therapy
Mitochondrial Trifunctional Protein blood
Muscular Diseases diet therapy
Muscular Diseases pathology
Muscular Diseases therapy
Nervous System Diseases diet therapy
Nervous System Diseases pathology
Nervous System Diseases therapy
Racemases and Epimerases genetics
Racemases and Epimerases metabolism
Rhabdomyolysis diet therapy
Rhabdomyolysis pathology
Rhabdomyolysis therapy
Cardiomyopathies blood
Carnitine analogs & derivatives
Carnitine O-Palmitoyltransferase deficiency
Congenital Bone Marrow Failure Syndromes blood
Lipid Metabolism, Inborn Errors blood
Metabolism, Inborn Errors blood
Mitochondrial Diseases blood
Mitochondrial Myopathies blood
Mitochondrial Trifunctional Protein deficiency
Muscular Diseases blood
Nervous System Diseases blood
Rhabdomyolysis blood

Details

Language :
English
ISSN :
1096-7206
Volume :
131
Issue :
1-2
Database :
MEDLINE
Journal :
Molecular genetics and metabolism
Publication Type :
Academic Journal
Accession number :
32928639
Full Text :
https://doi.org/10.1016/j.ymgme.2020.09.001