Abstract
We describe a method for the diagnosis of mitochondrial fatty acid oxidation disorders that is based on the analysis of acylcarnitine and acyl-coenzyme A (acyl-CoA) esters generated during fatty acid oxidation by permeabilized skin fibroblasts. This method requires only small amounts of cultured fibroblasts with minimal preparation, and no isolation of mitochondrial fractions is necessary. During oxidation of [U-14C]hexadecanoate, normal human fibroblasts from patients with fatty acid oxidation defects show a completely different pattern of intermediates, and in each case the observed profile reflects the site of the defect. The diagnosis and likely site of a mitochondrial fatty acid oxidation defect can be made readily from two 80-cm2 culture flasks of fibroblasts with this technique.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acyl Coenzyme A / metabolism*
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Acyl-CoA Dehydrogenase
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Acyl-CoA Dehydrogenase, Long-Chain
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Carbon Radioisotopes
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Carnitine / metabolism
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Carnitine Acyltransferases / deficiency
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Carnitine O-Palmitoyltransferase / deficiency
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Cells, Cultured
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Chromatography, High Pressure Liquid
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Fatty Acid Desaturases / deficiency
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Fatty Acids / metabolism*
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Fibroblasts / metabolism*
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Humans
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Lipid Metabolism, Inborn Errors / diagnosis*
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Lipid Metabolism, Inborn Errors / metabolism
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Mitochondria / metabolism*
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Oxidation-Reduction
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Palmitic Acids / metabolism
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Reproducibility of Results
Substances
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Acyl Coenzyme A
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Carbon Radioisotopes
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Fatty Acids
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Palmitic Acids
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Fatty Acid Desaturases
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Acyl-CoA Dehydrogenase
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Acyl-CoA Dehydrogenase, Long-Chain
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Carnitine Acyltransferases
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Carnitine O-Palmitoyltransferase
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Carnitine