Literature DB >> 17524384

Diagnosis of X-linked adrenoleukodystrophy in blood leukocytes.

Ursula Unterberger1, Günther Regelsberger, Regina Sundt, Hanno Bernheimer, Till Voigtländer.   

Abstract

OBJECTIVES: Our aim was to replace cultured skin fibroblasts in the diagnosis of X-linked adrenoleukodystrophy (X-ALD) by peripheral blood cells. DESIGN AND METHODS: Very long chain fatty acids (VLCFAs) were analyzed in leukocytes from X-ALD patients, heterozygotes, and controls using gas chromatography-mass spectrometry (GC-MS). Immunofluorescence for adrenoleukodystrophy protein (ALDP) was performed in mononuclear blood cell preparations of X-ALD patients known to be ALDP negative in fibroblasts, heterozygote relatives of these patients, and controls.
RESULTS: All X-ALD patients were distinguishable from controls by VLCFA analysis in leukocytes. 91.7% of heterozygotes were identified by combined VLCFA analysis in leukocytes and plasma. All patients investigated lacked ALDP immunoreactivity in mononuclear cells, while heterozygotes showed mosaic patterns of positive and negative cells.
CONCLUSION: Determination of VLCFAs by GC-MS in combination with ALDP immunofluorescence in peripheral blood cells provides a fast and minimally invasive diagnostic method for X-ALD, which, in contrast to plasma analysis, is independent of alimentary influences. Notably, joint evaluation of leukocytes and plasma considerably improves the identification of heterozygotes.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17524384     DOI: 10.1016/j.clinbiochem.2007.04.015

Source DB:  PubMed          Journal:  Clin Biochem        ISSN: 0009-9120            Impact factor:   3.281


  6 in total

1.  Lymphoblastoid cell lines for diagnosis of peroxisome biogenesis disorders.

Authors:  Sabine Grønborg; Ralph Krätzner; Hendrik Rosewich; Jutta Gärtner
Journal:  JIMD Rep       Date:  2011-06-22

2.  The impact of a ketogenic diet and liver dysfunction on serum very long-chain fatty acids levels.

Authors:  T J Stradomska; M Bachański; J Pawłowska; M Syczewska; A Stolarczyk; A Tylki-Szymańska
Journal:  Lipids       Date:  2013-01-31       Impact factor: 1.880

Review 3.  The genetic landscape of X-linked adrenoleukodystrophy: inheritance, mutations, modifier genes, and diagnosis.

Authors:  Christoph Wiesinger; Florian S Eichler; Johannes Berger
Journal:  Appl Clin Genet       Date:  2015-05-02

4.  Abcd2 is a strong modifier of the metabolic impairments in peritoneal macrophages of ABCD1-deficient mice.

Authors:  Zahid Muneer; Christoph Wiesinger; Till Voigtländer; Hauke B Werner; Johannes Berger; Sonja Forss-Petter
Journal:  PLoS One       Date:  2014-09-25       Impact factor: 3.240

5.  X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism is severely impaired in monocytes but not in lymphocytes.

Authors:  Franziska D Weber; Christoph Wiesinger; Sonja Forss-Petter; Günther Regelsberger; Angelika Einwich; Willi H A Weber; Wolfgang Köhler; Hannes Stockinger; Johannes Berger
Journal:  Hum Mol Genet       Date:  2013-12-20       Impact factor: 6.150

6.  Impaired very long-chain acyl-CoA β-oxidation in human X-linked adrenoleukodystrophy fibroblasts is a direct consequence of ABCD1 transporter dysfunction.

Authors:  Christoph Wiesinger; Markus Kunze; Günther Regelsberger; Sonja Forss-Petter; Johannes Berger
Journal:  J Biol Chem       Date:  2013-05-13       Impact factor: 5.157

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.