Effect of Feeding, Exercise, and Genotype on Plasma 3-Hydroxyacylcarnitines in Children With LCHAD Deficiency
2009
Gillingham, Melanie B. | Matern, Dietrich | Harding, Cary O.
Chronic complications observed in patients with long-chain 3-hydroxyacyl coenzyme A dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency may be mediated by the accumulation of 3-hydroxy fatty acid compounds. To understand variation in metabolite accumulation, 3-hydroxyacylcarnitine concentrations were measured by tandem mass spectrometry before and after a mixed meal and moderate-intensity exercise. Subjects who were homozygous or heterozygous for the common mutation (c.1528G > C) in the TFP alpha subunit (LCHAD deficiency) had significantly higher 3-hydroxyacylcarnitines than subjects with TFP deficiency. Feeding a mixed meal significantly suppressed and exercise significantly increased plasma 3-hydroxyacylcarnitines concentrations.
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