Literature DB >> 7785942

Rapid diagnosis of long chain and medium chain fatty acid oxidation disorders using lymphocytes.

M Brivet1, A Slama, J M Saudubray, A Legrand, A Lemonnier.   

Abstract

A method based on the release of tritiated water from [9,10(n)-3H] palmitic and myristic acids previously described for fibroblasts, was adapted for lymphocytes for the rapid diagnosis of fatty acid oxidation disorders. Optimal concentrations for both substrates and linearity of the assay were established. Normal values were established in control subjects of different age groups (58 children and 117 adults) and 16 patients with known fatty acid oxidation disorders were tested. Tritiated water production from patients' lymphocytes was expressed as a ratio between residual oxidations of palmitate and myristate and the results show that this method allows good differentiation between long chain and medium chain fatty acid oxidation defects.

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Year:  1995        PMID: 7785942     DOI: 10.1177/000456329503200204

Source DB:  PubMed          Journal:  Ann Clin Biochem        ISSN: 0004-5632            Impact factor:   2.057


  12 in total

1.  A simple screening test for fatty acid oxidation defects using whole-blood palmitate oxidation.

Authors:  L E Seargeant; K Balachandra; C Mallory; L A Dilling; C R Greenberg
Journal:  J Inherit Metab Dis       Date:  1999-08       Impact factor: 4.982

Review 2.  Genetic hypoglycaemia in infancy and childhood: pathophysiology and diagnosis.

Authors:  J M Saudubray; P de Lonlay; G Touati; D Martin; M C Nassogne; P Castelnau; C Sevin; C Laborde; C Baussan; M Brivet; A Vassault; D Rabier; J P Bonnefont; P Kamoun
Journal:  J Inherit Metab Dis       Date:  2000-05       Impact factor: 4.982

3.  Multiple sources of metabolic disturbance in ETHE1-related ethylmalonic encephalopathy.

Authors:  Magalie Barth; Chris Ottolenghi; Laurence Hubert; Dominique Chrétien; Valérie Serre; Stéphanie Gobin; Stéphane Romano; Anne Vassault; Aziz Sefiani; Daniel Ricquier; Nathalie Boddaert; Michèle Brivet; Yves de Keyzer; Arnold Munnich; Marinus Duran; Daniel Rabier; Vassili Valayannopoulos; Pascale de Lonlay
Journal:  J Inherit Metab Dis       Date:  2010-10-27       Impact factor: 4.982

Review 4.  Compromised fatty acid oxidation in mitochondrial disorders.

Authors:  L Hagenfeldt
Journal:  J Inherit Metab Dis       Date:  1998-08       Impact factor: 4.982

5.  Disrupting the CH1 domain structure in the acetyltransferases CBP and p300 results in lean mice with increased metabolic control.

Authors:  David C Bedford; Lawryn H Kasper; Ruoning Wang; Yunchao Chang; Douglas R Green; Paul K Brindle
Journal:  Cell Metab       Date:  2011-08-03       Impact factor: 27.287

6.  Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients.

Authors:  Julien Baruteau; Philippe Sachs; Pierre Broué; Michèle Brivet; Hendy Abdoul; Christine Vianey-Saban; Hélène Ogier de Baulny
Journal:  J Inherit Metab Dis       Date:  2012-10-03       Impact factor: 4.982

Review 7.  Defects in activation and transport of fatty acids.

Authors:  M Brivet; A Boutron; A Slama; C Costa; L Thuillier; F Demaugre; D Rabier; J M Saudubray; J P Bonnefont
Journal:  J Inherit Metab Dis       Date:  1999-06       Impact factor: 4.982

8.  Improved detection of long-chain fatty acid oxidation defects in intact cells using [9,10-3H]oleic acid.

Authors:  S E Olpin; N J Manning; R J Pollitt; S Clarke
Journal:  J Inherit Metab Dis       Date:  1997-07       Impact factor: 4.982

9.  Palmitoyl-carnitine production by blood cells associates with the concentration of circulating acyl-carnitines in healthy overweight women.

Authors:  Maria Chondronikola; Rabia Asghar; Xiaojun Zhang; Edgar L Dillon; William J Durham; Zhanpin Wu; Craig Porter; Maria Camacho-Hughes; Yingxin Zhao; Allan R Brasier; Elena Volpi; Melinda Sheffield-Moore; Nicola Abate; Labros Sidossis; Demidmaa Tuvdendorj
Journal:  Clin Nutr       Date:  2016-09-06       Impact factor: 7.324

10.  A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report.

Authors:  Anne-Frédérique Dessein; Monique Fontaine; Brage S Andresen; Niels Gregersen; Michèle Brivet; Daniel Rabier; Silvia Napuri-Gouel; Dries Dobbelaere; Karine Mention-Mulliez; Annie Martin-Ponthieu; Gilbert Briand; David S Millington; Christine Vianey-Saban; Ronald J A Wanders; Joseph Vamecq
Journal:  Orphanet J Rare Dis       Date:  2010-10-05       Impact factor: 4.123

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