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Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency
BACKGROUND: Multiple Acyl-CoA-Dehydrogenase deficiency (MADD) is an inherited metabolic disorder characterized by impaired oxidation of fatty acids and some amino acids. METHODS: We were interested whether children with MADD could tolerate a prolonged low-intensity exercise test and if this test cou...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1159171/ https://www.ncbi.nlm.nih.gov/pubmed/15907213 http://dx.doi.org/10.1186/1743-7075-2-12 |
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author | Takken, T Custers, J WH Visser, G Dorland, L Helders, PJM de Koning, TJ |
author_facet | Takken, T Custers, J WH Visser, G Dorland, L Helders, PJM de Koning, TJ |
author_sort | Takken, T |
collection | PubMed |
description | BACKGROUND: Multiple Acyl-CoA-Dehydrogenase deficiency (MADD) is an inherited metabolic disorder characterized by impaired oxidation of fatty acids and some amino acids. METHODS: We were interested whether children with MADD could tolerate a prolonged low-intensity exercise test and if this test could have any additional diagnostic value. Therefore, we performed a maximal exercise test and a low-intensity prolonged exercise test in 2 patients with MADD and in 5 control subjects. During a prolonged exercise test the subjects exercised on a cycle ergometer at a constant workload of 30% of their maximum for 90 minutes and heart rate, oxygen uptake, fuel utilization and changes in relevant blood and urinary parameters were monitored. RESULTS: The tests were tolerated well. During the prolonged exercise test the fatty acid oxidation (FAO) was quite low compared to 5 control subjects, while characteristic metabolites of MADD appeared in plasma and urine. CONCLUSION: We suggest that the prolonged exercise test could be of diagnostic importance and might replace the fasting test as a diagnostic procedure in some cases, particularly in patients with anamnestic signs of intolerance for prolonged exercise. |
format | Text |
id | pubmed-1159171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-11591712005-06-25 Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency Takken, T Custers, J WH Visser, G Dorland, L Helders, PJM de Koning, TJ Nutr Metab (Lond) Research BACKGROUND: Multiple Acyl-CoA-Dehydrogenase deficiency (MADD) is an inherited metabolic disorder characterized by impaired oxidation of fatty acids and some amino acids. METHODS: We were interested whether children with MADD could tolerate a prolonged low-intensity exercise test and if this test could have any additional diagnostic value. Therefore, we performed a maximal exercise test and a low-intensity prolonged exercise test in 2 patients with MADD and in 5 control subjects. During a prolonged exercise test the subjects exercised on a cycle ergometer at a constant workload of 30% of their maximum for 90 minutes and heart rate, oxygen uptake, fuel utilization and changes in relevant blood and urinary parameters were monitored. RESULTS: The tests were tolerated well. During the prolonged exercise test the fatty acid oxidation (FAO) was quite low compared to 5 control subjects, while characteristic metabolites of MADD appeared in plasma and urine. CONCLUSION: We suggest that the prolonged exercise test could be of diagnostic importance and might replace the fasting test as a diagnostic procedure in some cases, particularly in patients with anamnestic signs of intolerance for prolonged exercise. BioMed Central 2005-05-20 /pmc/articles/PMC1159171/ /pubmed/15907213 http://dx.doi.org/10.1186/1743-7075-2-12 Text en Copyright © 2005 Takken et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Takken, T Custers, J WH Visser, G Dorland, L Helders, PJM de Koning, TJ Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency |
title | Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency |
title_full | Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency |
title_fullStr | Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency |
title_full_unstemmed | Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency |
title_short | Prolonged exercise testing in two children with a mild Multiple Acyl-CoA-Dehydrogenase deficiency |
title_sort | prolonged exercise testing in two children with a mild multiple acyl-coa-dehydrogenase deficiency |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1159171/ https://www.ncbi.nlm.nih.gov/pubmed/15907213 http://dx.doi.org/10.1186/1743-7075-2-12 |
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