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Effects of fasting, feeding and exercise on plasma acylcarnitines among subjects with CPT2D, VLCADD and LCHADD/TFPD.
Elizondo, Gabriela; Matern, Dietrich; Vockley, Jerry; Harding, Cary O; Gillingham, Melanie B.
Afiliación
  • Elizondo G; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, Oregon, United States of America.
  • Matern D; Biochemical Genetics Laboratory, Mayo Clinic, Rochester, MN, United States of America.
  • Vockley J; Department of Pediatrics University of Pittsburgh School of Medicine, Center for Rare Disease Therapy, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, United States of America.
  • Harding CO; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, Oregon, United States of America.
  • Gillingham MB; Department of Molecular and Medical Genetics, Oregon Health & Science University, Portland, Oregon, United States of America; Biochemical Genetics Laboratory, Mayo Clinic, Rochester, MN, United States of America. Electronic address: gillingm@ohsu.edu.
Mol Genet Metab ; 131(1-2): 90-97, 2020.
Article en En | MEDLINE | ID: mdl-32928639
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.

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.

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.

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.
Asunto(s)
Cardiomiopatías/sangre; Carnitina O-Palmitoiltransferasa/deficiencia; Carnitina/análogos & derivados; Síndromes Congénitos de Insuficiencia de la Médula Ósea/sangre; Errores Innatos del Metabolismo Lipídico/sangre; Errores Innatos del Metabolismo/sangre; Enfermedades Mitocondriales/sangre; Miopatías Mitocondriales/sangre; Proteína Trifuncional Mitocondrial/deficiencia; Enfermedades Musculares/sangre; Enfermedades del Sistema Nervioso/sangre; Rabdomiólisis/sangre; 3-Hidroxiacil-CoA Deshidrogenasas/genética; 3-Hidroxiacil-CoA Deshidrogenasas/metabolismo; Acetil-CoA C-Aciltransferasa/genética; Acetil-CoA C-Aciltransferasa/metabolismo; Acil-CoA Deshidrogenasa de Cadena Larga/sangre; Isomerasas de Doble Vínculo Carbono-Carbono/genética; Isomerasas de Doble Vínculo Carbono-Carbono/metabolismo; Cardiomiopatías/dietoterapia; Cardiomiopatías/patología; Cardiomiopatías/terapia; Carnitina/sangre; Carnitina/genética; Carnitina/metabolismo; Carnitina O-Palmitoiltransferasa/sangre; Síndromes Congénitos de Insuficiencia de la Médula Ósea/dietoterapia; Síndromes Congénitos de Insuficiencia de la Médula Ósea/patología; Síndromes Congénitos de Insuficiencia de la Médula Ósea/terapia; Enoil-CoA Hidratasa/genética; Enoil-CoA Hidratasa/metabolismo; Terapia por Ejercicio; Ayuno; Femenino; Humanos; Errores Innatos del Metabolismo Lipídico/dietoterapia; Errores Innatos del Metabolismo Lipídico/patología; Errores Innatos del Metabolismo Lipídico/terapia; 3-Hidroxiacil-CoA Deshidrogenasa de Cadena Larga/sangre; Masculino; Errores Innatos del Metabolismo/dietoterapia; Errores Innatos del Metabolismo/patología; Errores Innatos del Metabolismo/terapia; Enfermedades Mitocondriales/dietoterapia; Enfermedades Mitocondriales/patología; Enfermedades Mitocondriales/terapia; Miopatías Mitocondriales/dietoterapia; Miopatías Mitocondriales/patología; Miopatías Mitocondriales/terapia; Proteína Trifuncional Mitocondrial/sangre; Enfermedades Musculares/dietoterapia; Enfermedades Musculares/patología; Enfermedades Musculares/terapia; Enfermedades del Sistema Nervioso/dietoterapia; Enfermedades del Sistema Nervioso/patología; Enfermedades del Sistema Nervioso/terapia; Racemasas y Epimerasas/genética; Racemasas y Epimerasas/metabolismo; Rabdomiólisis/dietoterapia; Rabdomiólisis/patología; Rabdomiólisis/terapia
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Rabdomiólisis / Carnitina / Carnitina O-Palmitoiltransferasa / Miopatías Mitocondriales / Enfermedades Mitocondriales / Proteína Trifuncional Mitocondrial / Síndromes Congénitos de Insuficiencia de la Médula Ósea / Errores Innatos del Metabolismo Lipídico / Errores Innatos del Metabolismo / Enfermedades Musculares Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Rabdomiólisis / Carnitina / Carnitina O-Palmitoiltransferasa / Miopatías Mitocondriales / Enfermedades Mitocondriales / Proteína Trifuncional Mitocondrial / Síndromes Congénitos de Insuficiencia de la Médula Ósea / Errores Innatos del Metabolismo Lipídico / Errores Innatos del Metabolismo / Enfermedades Musculares Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos