Literature DB >> 6429435

Stable isotope dilution analysis of 3-hydroxyisovaleric acid in amniotic fluid: contribution to the prenatal diagnosis of inherited disorders of leucine catabolism.

C Jakobs, L Sweetman, W L Nyhan, S Packman.   

Abstract

A quantitative assay for 3-hydroxyisovaleric acid in amniotic fluid was developed using D6-3-hydroxyisovaleric acid as an internal standard. 3-Hydroxyisovaleric acid was isolated by liquid partition chromatography and the amount determined by selected ion monitoring, ammonia chemical ionization gas chromatography-mass spectrometry of the trimethylsilyl derivatives. The concentration of 3-hydroxyisovaleric acid in ten normal amniotic fluid was 4.52 +/- 1.73 mumol/l. The level was elevated eight-fold in the amniotic fluid from a pregnancy resulting in the birth of a child with biotin-responsive multiple carboxylase deficiency. The stable isotope dilution assay of 3-hydroxyisovaleric acid in amniotic fluid is a rapid, sensitive and accurate method for the prenatal diagnosis of this disorder, and may be of value in the prenatal diagnosis of other inherited disorders of leucine catabolism.

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Year:  1984        PMID: 6429435     DOI: 10.1007/bf01805614

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  16 in total

Review 1.  Selective ion monitoring in clinical chemistry.

Authors:  I Björkhem
Journal:  CRC Crit Rev Clin Lab Sci       Date:  1979-08

2.  Beta-methylcrotonyl-CoA carboxylase deficiency: a new metabolic error in leucine degradation.

Authors:  O Stokke; L Eldjarn; E Jellum; H Pande; P E Waaler
Journal:  Pediatrics       Date:  1972-05       Impact factor: 7.124

3.  Inherited 3-methylglutaconic aciduria in two brothers--another defect of leucine metabolism.

Authors:  M Duran; F A Beemer; A S Tibosch; L Bruinvis; D Ketting; S K Wadman
Journal:  J Pediatr       Date:  1982-10       Impact factor: 4.406

4.  Deficient biotinidase activity in late-onset multiple carboxylase deficiency.

Authors:  B Wolf; R E Grier; W D Parker; S I Goodman; R J Allen
Journal:  N Engl J Med       Date:  1983-01-20       Impact factor: 91.245

5.  Pitfalls in the prenatal diagnosis of propionic acidemia.

Authors:  P D Buchanan; S G Kahler; L Sweetman; W L Nyhan
Journal:  Clin Genet       Date:  1980-09       Impact factor: 4.438

6.  The neonatal form of biotin-responsive multiple carboxylase deficiency.

Authors:  S Packman; L Sweetman; H Baker; S Wall
Journal:  J Pediatr       Date:  1981-09       Impact factor: 4.406

7.  Propionyl-CoA carboxylase deficiency in a patient with biotin-responsive 3-methylcrotonylglycinuria.

Authors:  L Sweetman; S P Bates; D Hull; W L Nyhan
Journal:  Pediatr Res       Date:  1977-11       Impact factor: 3.756

8.  Biotin-response organicaciduria. Multiple carboxylase defects and complementation studies with propionicacidemia in cultured fibroblasts.

Authors:  M Saunders; L Sweetman; B Robinson; K Roth; R Cohn; R A Gravel
Journal:  J Clin Invest       Date:  1979-12       Impact factor: 14.808

9.  Mutant holocarboxylase synthetase: evidence for the enzyme defect in early infantile biotin-responsive multiple carboxylase deficiency.

Authors:  B J Burri; L Sweetman; W L Nyhan
Journal:  J Clin Invest       Date:  1981-12       Impact factor: 14.808

10.  Organic acid excretion in a patient with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency: facts and artefacts.

Authors:  M Duran; D Ketting; S K Wadman; C Jakobs; R B Schutgens; H A Veder
Journal:  Clin Chim Acta       Date:  1978-12-01       Impact factor: 3.786

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  8 in total

1.  Assessment of an electron-impact GC-MS method for organic acids and glycine conjugates in amniotic fluid.

Authors:  A Kumps; E Vamos; Y Mardens; M Abramowicz; J Genin; P Duez
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

2.  Prenatal diagnosis of 3-hydroxy-3-methylglutaric aciduria by GC-MS and enzymology on cultured amniocytes and chorionic villi.

Authors:  R A Chalmers; B M Tracey; J Mistry; T E Stacey; I R McFadyen
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

Review 3.  Prenatal diagnosis of inherited metabolic diseases.

Authors:  R Diukman; J D Goldberg
Journal:  West J Med       Date:  1993-09

4.  Prenatal diagnosis of the organic acidurias.

Authors:  L Sweetman
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

Review 5.  Prenatal diagnosis of inborn errors of metabolism with renal manifestations.

Authors:  E Harms
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714

6.  Isolated biotin-resistant deficiency of 3-methylcrotonyl-CoA carboxylase presenting as a clinically severe form in a newborn with fatal outcome.

Authors:  C Bannwart; B Wermuth; R Baumgartner; T Suormala; U N Weismann
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

Review 7.  Screening for defects of branched-chain amino acid metabolism.

Authors:  K M Gibson; C F Lee; G F Hoffmann
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

8.  Accumulated Metabolites of Hydroxybutyric Acid Serve as Diagnostic and Prognostic Biomarkers of Ovarian High-Grade Serous Carcinomas.

Authors:  Silvia Darb-Esfahani; Elena Ioana Braicu; Mika Hilvo; Ines de Santiago; Peddinti Gopalacharyulu; Wolfgang D Schmitt; Jan Budczies; Marc Kuhberg; Manfred Dietel; Tero Aittokallio; Florian Markowetz; Carsten Denkert; Jalid Sehouli; Christian Frezza
Journal:  Cancer Res       Date:  2015-12-18       Impact factor: 12.701

  8 in total

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