Quantitative analysis of urinary acylglycines for the diagnosis of beta-oxidation defects using GC-NCI-MS

J Pharm Biomed Anal. 2000 Jan;21(6):1215-24. doi: 10.1016/s0731-7085(99)00235-6.

Abstract

The analysis of acylglycines is an important biochemical tool for the diagnosis of inherited disorders of mitochondrial fatty acid beta-oxidation. A stable isotope dilution gas chromatography negative chemical ionisation mass spectrometry method for the quantitative analysis of short- and medium-chain acylglycines as their bis(trifluoromethyl)benzyl (BTFMB) ester derivatives is described. The diagnostic usefulness of the method was demonstrated in nine patients with medium-chain acyl-coenzyme A (CoA) dehydrogenase (MCAD) deficiency, and seven patients with multiple acyl-CoA dehydrogenation defect (MAD). The urinary acylglycine profiles in these patients were compared to those in controls (n = 19), children on a medium-chain triglyceride (MCT) supplemented diet (n = 4), and patients with various other diseases (n = 5).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acyl Coenzyme A / metabolism
  • Acyl-CoA Dehydrogenase
  • Child
  • Child, Preschool
  • Fatty Acid Desaturases / deficiency
  • Fatty Acid Desaturases / metabolism
  • Gas Chromatography-Mass Spectrometry / methods*
  • Glycine / urine*
  • Humans
  • Infant
  • Infant, Newborn
  • Lipid Metabolism, Inborn Errors / diagnosis*
  • Lipid Metabolism, Inborn Errors / urine
  • Mitochondria / metabolism
  • Oxidation-Reduction
  • Reference Values
  • Reproducibility of Results
  • Sensitivity and Specificity

Substances

  • Acyl Coenzyme A
  • Fatty Acid Desaturases
  • Acyl-CoA Dehydrogenase
  • Glycine