Literature DB >> 1635814

Urinary medium-chain acylcarnitines in medium-chain acyl-CoA dehydrogenase deficiency, medium-chain triglyceride feeding and valproic acid therapy: sensitivity and specificity of the radioisotopic exchange/high performance liquid chromatography method.

E Schmidt-Sommerfeld1, D Penn, P Rinaldo, D Kossak, B U Li, Z H Huang, D A Gage.   

Abstract

To determine the sensitivity and specificity of detecting urinary medium-chain acylcarnitines for the diagnosis of MCAD deficiency, 114 urine specimens from 75 children with metabolic diseases and controls were analyzed in a blinded fashion using a radioisotopic exchange/HPLC method. All 47 patients with MCAD deficiency were correctly diagnosed using the criterion hexanoylcarnitine or octanoylcarnitine peak areas larger than those of other medium-chain acylcarnitines. The majority of them were tested during the asymptomatic state without L-carnitine loading. Four patients with other defects of fatty acid oxidation and three patients receiving valproic acid had a similar acylcarnitine excretion pattern. To further examine the specificity of the method, eight infants receiving a diet enriched with medium-chain triglycerides and 13 additional patients receiving valproic acid were studied. Most of these also tested positive for MCAD deficiency by the above criterion. Analysis by a new gas chromatographic-mass spectrometric procedure revealed that octanoylcarnitine, not valproylcarnitine, was the most abundant medium-chain carnitine ester excreted by a patient treated with valproic acid. Quantitation of urinary hexanoylcarnitine and octanoylcarnitine showed considerable overlap among patients with MCAD deficiency and those receiving valproic acid or a medium-chain triglyceride-enriched diet. MCAD deficiency can be reliably detected in urine specimens by this method without the need for prior carnitine loading. However, other defects in fatty acid oxidation must be differentiated from MCAD deficiency, and a history of medium-chain triglyceride or valproic acid administration must be considered if the diagnosis of MCAD deficiency is sought through analysis of urinary acylcarnitines.

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Year:  1992        PMID: 1635814     DOI: 10.1203/00006450-199206000-00002

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  5 in total

Review 1.  Acylcarnitines in intermediary metabolism.

Authors:  A C Sewell; H J Böhles
Journal:  Eur J Pediatr       Date:  1995-11       Impact factor: 3.183

Review 2.  Pharmacokinetics of L-carnitine.

Authors:  Allan M Evans; Gianfranco Fornasini
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

3.  Metabolomic analysis identifies differentially produced oral metabolites, including the oncometabolite 2-hydroxyglutarate, in patients with head and neck squamous cell carcinoma.

Authors:  Pranab K Mukherjee; Pauline Funchain; Mauricio Retuerto; Richard J Jurevic; Nicole Fowler; Brian Burkey; Charis Eng; Mahmoud A Ghannoum
Journal:  BBA Clin       Date:  2016-12-18

4.  Molecular signature of renal cell carcinoma by means of a multiplatform metabolomics analysis.

Authors:  Marta Kordalewska; Renata Wawrzyniak; Julia Jacyna; Joanna Godzień; Ángeles López Gonzálves; Joanna Raczak-Gutknecht; Marcin Markuszewski; Piotr Gutknecht; Marcin Matuszewski; Janusz Siebert; Coral Barbas; Michał J Markuszewski
Journal:  Biochem Biophys Rep       Date:  2022-08-04

5.  1H-Nuclear Magnetic Resonance Analysis of Urine as Diagnostic Tool for Organic Acidemias and Aminoacidopathies.

Authors:  Ninna Pulido; Johana M Guevara-Morales; Alexander Rodriguez-López; Álvaro Pulido; Jhon Díaz; Ru Angelie Edrada-Ebel; Olga Y Echeverri-Peña
Journal:  Metabolites       Date:  2021-12-20
  5 in total

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