Literature DB >> 1653652

Facts and artefacts in mevalonic aciduria: development of a stable isotope dilution GCMS assay for mevalonic acid and its application to physiological fluids, tissue samples, prenatal diagnosis and carrier detection.

G F Hoffmann1, L Sweetman, H J Bremer, D H Hunneman, J Hyánek, V Kozich, W Lehnert, W L Nyhan, I Speidel, F K Trefz.   

Abstract

A stable isotope dilution assay using D3-mevalonic acid was developed and applied to the study of mevalonic aciduria. The method also appears to be suitable for the evaluation of different therapeutic regimens in patients with hypercholesterolemia. Mevalonic acid was isolated by liquid partition chromatography and quantified as the underivatized lactone by means of ammonia chemical ionization selected ion monitoring capillary gas chromatography-mass spectrometry. In heterozygotes there was significantly greater urinary excretion of mevalonic acid, while the range of enzymatic activity of mevalonate kinase showed an overlap with that of controls. The analysis of amniotic fluids of two pregnancies at risk for mevalonic aciduria showed a 3277-fold elevation as compared to controls in the first case, diagnostic of an affected fetus, and a normal value in the second one. Mevalonic acid concentration was much increased in tissues of the affected and aborted fetus. Concentrations ranged from 840 to 1120 mumol/kg in various tissues and were as high as 1810 mumol/kg in brain. Concentrations in control fetal tissues were approximately 1 mumol/kg.

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Year:  1991        PMID: 1653652     DOI: 10.1016/0009-8981(91)90355-g

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


  6 in total

1.  Mevalonate kinase deficiency in a dizygotic twin with mild mevalonic aciduria.

Authors:  K M Gibson; G F Hoffmann; L Sweetman; B Buckingham
Journal:  J Inherit Metab Dis       Date:  1997-07       Impact factor: 4.982

2.  Pitfalls in aminoacid and organic acid analysis: 3-hydroxypropionic aciduria.

Authors:  C Bachmann; O Boulat; B J Meyrat; J P Colombo; P Pilloud
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

3.  Regulation of cholesterol biosynthetic pathway in patients with the Smith-Lemli-Opitz syndrome.

Authors:  M Honda; G S Tint; A Honda; G Salen; S Shefer; A K Batta; Y Matsuzaki; N Tanaka
Journal:  J Inherit Metab Dis       Date:  2000-07       Impact factor: 4.982

4.  Mevalonate kinase assay using DEAE-cellulose column chromatography for first-trimester prenatal diagnosis and complementation analysis in mevalonic aciduria.

Authors:  G F Hoffmann; S U Brendel; S R Scharfschwerdt; Y S Shin; I M Speidel; K M Gibson
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

Review 5.  Neurological manifestations of organic acid disorders.

Authors:  G F Hoffmann; K M Gibson; F K Trefz; W L Nyhan; H J Bremer; D Rating
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

Review 6.  Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndrome.

Authors:  Dorothea Haas; Georg F Hoffmann
Journal:  Orphanet J Rare Dis       Date:  2006-04-26       Impact factor: 4.123

  6 in total

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