Literature DB >> 11229423

Fasting medium chain acyl-coenzyme A dehydrogenase--deficient children can make ketones.

J M Fletcher1, J J Pitt.   

Abstract

Medium chain acyl-coenzyme A dehydrogenase (MCAD) deficiency classically presents as hypoketotic hypoglycemia. Under-production of ketones has been presumed to be the cause of hypoketosis, but this has never been proven. Stable isotope dilution studies of ketone kinetics were performed on three well children with homozygous 985G MCAD deficiency using 1,3-13C2 sodium acetoacetate and 1,2,3,4-13C4 sodium 3-hydroxybutyrate to ascertain the rates of ketone production, interconversion, and use. All children were fasted for 9 to 11.5 hours before the beginning of the study period. Euglycemia was maintained in all cases. Ketone kinetics were calculated using a two-accessible pool model and showed normal ketone production in all three children compared with published control data from children fasted for a similar length of time. There is no evidence for underproduction or overuse of ketones in these MCAD-deficient children, at least when they are well. We propose that another factor, such as fever, may be required to reduce ketone production and result in the biochemical phenotype recognized in unwell children.

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Year:  2001        PMID: 11229423     DOI: 10.1053/meta.2001.20177

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


  7 in total

1.  Safe and unsafe duration of fasting for children with MCAD deficiency.

Authors:  Terry G J Derks; Francjan J van Spronsen; Jan Peter Rake; Christian S van der Hilst; Mark M Span; G Peter A Smit
Journal:  Eur J Pediatr       Date:  2006-06-21       Impact factor: 3.183

Review 2.  Prolonged QTc interval in association with medium-chain acyl-coenzyme A dehydrogenase deficiency.

Authors:  Jason R Wiles; Nancy Leslie; Timothy K Knilans; Henry Akinbi
Journal:  Pediatrics       Date:  2014-05-05       Impact factor: 7.124

Review 3.  Tolerance to fast: rational and practical evaluation in children with hypoketonaemia.

Authors:  J H Walter
Journal:  J Inherit Metab Dis       Date:  2009-03-04       Impact factor: 4.982

4.  Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort study.

Authors:  Catharina M L Touw; G Peter A Smit; Maaike de Vries; Johannis B C de Klerk; Annet M Bosch; Gepke Visser; Margot F Mulder; M Estela Rubio-Gozalbo; Bert Elvers; Klary E Niezen-Koning; Ronald J A Wanders; Hans R Waterham; Dirk-Jan Reijngoud; Terry G J Derks
Journal:  Orphanet J Rare Dis       Date:  2012-05-25       Impact factor: 4.123

Review 5.  Flux analysis of inborn errors of metabolism.

Authors:  D-J Reijngoud
Journal:  J Inherit Metab Dis       Date:  2018-01-09       Impact factor: 4.982

6.  Medium-chain acyl-CoA dehydrogenase deficiency: Two novel ACADM mutations identified in a retrospective screening.

Authors:  Andraz Smon; Urh Groselj; Marusa Debeljak; Mojca Zerjav Tansek; Sara Bertok; Magdalena Avbelj Stefanija; Katarina Trebusak Podkrajsek; Tadej Battelino; Barbka Repic Lampret
Journal:  J Int Med Res       Date:  2018-01-19       Impact factor: 1.671

7.  In vitro and in vivo consequences of variant medium-chain acyl-CoA dehydrogenase genotypes.

Authors:  Catharina M L Touw; G Peter A Smit; Klary E Niezen-Koning; Conny Bosgraaf-de Boer; Albert Gerding; Dirk-Jan Reijngoud; Terry G J Derks
Journal:  Orphanet J Rare Dis       Date:  2013-03-20       Impact factor: 4.123

  7 in total

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