Deuterated palmitate-driven acylcarnitine formation by whole-blood samples for a rapid diagnostic exploration of mitochondrial fatty acid oxidation disorders

Clin Chim Acta. 2009 Aug;406(1-2):23-6. doi: 10.1016/j.cca.2009.04.026. Epub 2009 May 5.

Abstract

Background: The biochemical diagnosis of mitochondrial fatty acid oxidation defects (FAOD) currently rests on enzyme assays. A dynamic ex vivo exploration consisting of incubations of whole-blood samples with stable-labeled palmitate and determining leukocyte capacities to produce deuterated acylcarnitines was developed on healthy controls (n=52) and patients with very-long- (VLCADD) (n=2), medium- (MCADD) (n=6), or short- (SCADD) (n=1) chain acyl-CoA dehydrogenase deficiencies.

Methods: Incubations were optimized with L-carnitine and [16-(2)H(3), 15-(2)H(2)]-palmitate at 37 degrees C for various time periods on MCADD and control whole-blood samples. Labeled acylcarnitines were quantified by electrospray-ionization tandem mass spectrometry after thawing, extraction and derivatization to their butyl esters and the method was applied to patients with defects mentioned above.

Results: The production of acylcarnitines was linear until 6 h of incubation and optimal on 50 to 200 nmol deuterated substrate. A good discrimination between MCADD patient and control data was found, with median C8/C4 acylcarnitine production rate ratios of 81.0 (5th-95th percentile range: 16.6-209.9) and 0.21 (5th-95th percentile range: 0.06-0.79), respectively. The method also discriminated from controls the VLCADD and SCADD patients. Preliminary studies on a healthy control indicated that the storage at 4 degrees C does little or not alter capacities of whole-blood samples to generate labeled acylcarnitines over a period of 48 h.

Conclusion: The rapid management afforded by the method, its abilities to characterize patients and to work on whole-blood samples after a stay of 24-48 h at 4 degrees C make it promising for the diagnostic exploration of FAOD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyl-CoA Dehydrogenases / deficiency
  • Acyl-CoA Dehydrogenases / genetics
  • Adult
  • Blood Specimen Collection
  • Carnitine / analogs & derivatives*
  • Carnitine / biosynthesis
  • Carnitine / blood
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Deuterium / metabolism*
  • Fatty Acids / metabolism*
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Kinetics
  • Male
  • Mitochondrial Diseases / blood*
  • Mitochondrial Diseases / diagnosis*
  • Mitochondrial Diseases / genetics
  • Mitochondrial Diseases / metabolism
  • Mutation
  • Oxidation-Reduction
  • Palmitates / metabolism*
  • Time Factors

Substances

  • Fatty Acids
  • Palmitates
  • acylcarnitine
  • Deuterium
  • Acyl-CoA Dehydrogenases
  • Carnitine