Ketogenic effects of carnitine in patients with muscular dystrophy and cytochrome oxidase deficiency

Dennis J. Paulson*, George E. Hoganson, John Traxler, Robert Sufit, Henry Peters, Austin L. Shug

*Corresponding author for this work

Research output: Contribution to journalArticle

4 Scopus citations

Abstract

The effects of a single oral dose of carnitine on fasting-induced ketosis was investigated in four normal individuals, five patients with muscular dystrophy, and one patient with a generalized cytochrome c oxidase deficiency. Plasma carnitine, free fatty acids, glucose, insulin, and glucagon were also measured. Normal individuals showed an average 0.09 mm increase in blood β-hydroxybutyrate concentration during a 12- to 18-hr period of fasting and carnitine administration did not affect this response (average: 0.12 mm). Muscular dystrophy patients showed a greater fasting-induced elevation in β-hydroxybutyrate (average 0.29 mm) and carnitine administration greatly enhanced this ketogenic response (average 0.84 mm). The cytochrome c oxidase deficient patient showed an even larger increase in β-hydroxybutyrate with fasting (1.67 mm) and carnitine further augmented this ketotic effect (3.78 mm). Plasma free fatty acids were also elevated in patients that showed enhanced ketosis. Plasma glucagon concentration did not change, but insulin levels decreased during the 12- to 18-hr period of fasting; no major differences were found between controls and patients. These results indicate that some patients with muscular dystrophy and cytochrome c oxidase deficiency are more prone to develop ketosis than normal individuals and that carnitine administration enhances this response. Since both muscular dystrophy patients and the patient with cytochrome c oxidase deficiency had similar ketogenic responses, the data suggest that ketone body utilization may be impaired in these patients. The ability of l-carnitine to be ketogenic should be considered in the treatment of these patients.

Original languageEnglish (US)
Pages (from-to)40-47
Number of pages8
JournalBiochemical Medicine and Metabolic Biology
Volume39
Issue number1
DOIs
StatePublished - Feb 1988

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Biochemistry

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