Literature DB >> 11948802

Analysis of 3-hydroxydodecanedioic acid for studies of fatty acid metabolic disorders: preparation of stable isotope standards.

J S Chickos1, Barbara A Way, J Wilson, M Shaharuzzaman, J Laird, M Landt.   

Abstract

Current diagnostic tests to detect disorders of fatty acids metabolism, such as long-chain hydroxyacyl CoA dehydrogenase deficiency (LCHAD), are hampered by insensitivity or a long delay time required for results. Children with LCHAD deficiency are known to excrete 3-hydroxydicarboxylic acids with chain lengths of 10-16 carbons, but a quantitative method to measure excretion of these potentially diagnostically important compounds has not been reported. We report synthetic schemes for synthesis of 3-hydroxydodecanedioic acid and a di-deuterated analog, suitable for use in a stable-isotope dilution mass spectrometric analytical approach. Evaluation of several common derivatization protocols to produce a volatile derivative for gas chromatography determined that trimethylsyl derivatives produced the best efficiency and stability. Positive-ion chemical ionization mass spectrometry provided the greatest yield of characteristic ions. These results indicate the basic reagents needed to develop sensitive and accurate 3-hydroxydodecanedioic acid measurements for diagnosis of LCHAD deficiency and other fatty acid oxidation disorders. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 11948802      PMCID: PMC6807789          DOI: 10.1002/jcla.10033

Source DB:  PubMed          Journal:  J Clin Lab Anal        ISSN: 0887-8013            Impact factor:   2.352


  9 in total

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Journal:  Clin Chem       Date:  2000-02       Impact factor: 8.327

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Authors:  M J Bennett
Journal:  Ann Clin Biochem       Date:  1990-11       Impact factor: 2.057

3.  Clinical and biochemical presentation of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Authors:  L Hagenfeldt; N Venizelos; U von Döbeln
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

4.  Mitochondropathy presenting with non-ketotic hypoglycaemia as 3-hydroxydicarboxylic aciduria.

Authors:  E Mayatepek; R J Wanders; M Becker; H J Bremer; G F Hoffmann
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

5.  Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation.

Authors:  J A Ibdah; I Tein; C Dionisi-Vici; M J Bennett; L IJlst; B Gibson; R J Wanders; A W Strauss
Journal:  J Clin Invest       Date:  1998-09-15       Impact factor: 14.808

6.  Metabolic origin of urinary 3-hydroxy dicarboxylic acids.

Authors:  K Y Tserng; S J Jin
Journal:  Biochemistry       Date:  1991-03-05       Impact factor: 3.162

7.  Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine.

Authors:  P Rinaldo; J J O'Shea; P M Coates; D E Hale; C A Stanley; K Tanaka
Journal:  N Engl J Med       Date:  1988-11-17       Impact factor: 91.245

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Authors:  D S Millington; C R Roe; D A Maltby
Journal:  Biomed Mass Spectrom       Date:  1984-05

9.  Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Authors:  M J Bennett; M J Weinberger; W G Sherwood; A B Burlina
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

  9 in total
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4.  Metabolomic profiling of plasma from middle-aged and advanced-age male mice reveals the metabolic abnormalities of carnitine biosynthesis in metallothionein gene knockout mice.

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Journal:  Aging (Albany NY)       Date:  2021-12-01       Impact factor: 5.682

5.  Assessment of components related to flavor and taste in Tan-lamb meat under different silage-feeding regimens using integrative metabolomics.

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6.  Metabolic Profiling of Plasma in Patients with Irritable Bowel Syndrome after a 4-Week Starch- and Sucrose-Reduced Diet.

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  6 in total

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