Literature DB >> 6688766

Studies of urinary organic acid profiles of a patient with dihydrolipoyl dehydrogenase deficiency.

T Kuhara, T Shinka, Y Inoue, M Matsumoto, M Yoshino, Y Sakaguchi, I Matsumoto.   

Abstract

Using gas chromatography-mass spectrometry (GC/MS), urinary organic acid profile studies were carried out on a patient with dihydrolipoyl dehydrogenase (E3) deficiency. Elevated levels of 2-hydroxyglutaric acid, 2-hydroxyisocaproic acid and 2-oxoisocaproic acid were observed in addition to lactic acid, 2-oxoglutaric acid, 2-hydroxyisovaleric acid and 2-hydroxybutyric acid previously described in patients with E3 deficiency. The 2-oxoglutaric acid levels were significantly lowered after branched-chain amino acid restriction. In an acute period, the patient was slightly ketoacidotic and excreted larger amounts of 2-oxoglutaric acid and lactic acid than in a static period. It was shown that, prior to confirmatory enzyme studies, patients with E3 deficiency who were suspected to have atypical maple syrup urine disease or chronic lactic acidosis can be rapidly identified by GC/MS analysis of urinary acids.

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Year:  1983        PMID: 6688766     DOI: 10.1016/0009-8981(83)90398-4

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  9 in total

Review 1.  The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.

Authors:  Kavi P Patel; Thomas W O'Brien; Sankarasubramon H Subramony; Jonathan Shuster; Peter W Stacpoole
Journal:  Mol Genet Metab       Date:  2011-10-07       Impact factor: 4.797

2.  The spectrum of pyruvate dehydrogenase complex deficiency: clinical, biochemical and genetic features in 371 patients.

Authors:  Kavi P Patel; Thomas W O'Brien; Sankarasubramon H Subramony; Jonathan Shuster; Peter W Stacpoole
Journal:  Mol Genet Metab       Date:  2012-07       Impact factor: 4.797

3.  Identification of two missense mutations in a dihydrolipoamide dehydrogenase-deficient patient.

Authors:  T C Liu; H Kim; C Arizmendi; A Kitano; M S Patel
Journal:  Proc Natl Acad Sci U S A       Date:  1993-06-01       Impact factor: 11.205

Review 4.  D-2-Hydroxyglutaric aciduria: unravelling the biochemical pathway and the genetic defect.

Authors:  Eduard A Struys
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

5.  Dihydrolipoyl dehydrogenase deficiency: a therapeutic trial with branched-chain amino acid restriction.

Authors:  Y Sakaguchi; M Yoshino; S Aramaki; I Yoshida; F Yamashita; T Kuhara; I Matsumoto; T Hayashi
Journal:  Eur J Pediatr       Date:  1986-09       Impact factor: 3.183

6.  Organic acids in urine of patients with congenital lactic acidoses: an aid to differential diagnosis.

Authors:  R A Chalmers
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

Review 7.  Cell culture studies on patients with mitochondrial diseases: molecular defects in pyruvate dehydrogenase.

Authors:  B H Robinson
Journal:  J Bioenerg Biomembr       Date:  1988-06       Impact factor: 2.945

8.  Three genes for enzymes of the pyruvate dehydrogenase complex map to human chromosomes 3, 7, and X.

Authors:  S Olson; B J Song; T L Huh; Y T Chi; R L Veech; O W McBride
Journal:  Am J Hum Genet       Date:  1990-02       Impact factor: 11.025

Review 9.  Progress in understanding 2-hydroxyglutaric acidurias.

Authors:  Martijn Kranendijk; Eduard A Struys; Gajja S Salomons; Marjo S Van der Knaap; Cornelis Jakobs
Journal:  J Inherit Metab Dis       Date:  2012-03-06       Impact factor: 4.982

  9 in total

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