N-Carbamylglutamate Is an Effective Treatment for Acute Neonatal Hyperammonaemia in a Patient with Methylmalonic Aciduria
- PMID: 26907495
- DOI: 10.1159/000443630
N-Carbamylglutamate Is an Effective Treatment for Acute Neonatal Hyperammonaemia in a Patient with Methylmalonic Aciduria
Abstract
N-carbamylglutamate (NCG) has been used in combination with ammonia scavengers (sodium benzoate, sodium phenylbutyrate) and dialysis to treat hyperammonaemia in methylmalonic aciduria (MMA). The sole use of NCG for acute neonatal hyperammonaemia secondary to MMA is demonstrated in a neonate presenting at day 9 with encephalopathy, severe metabolic acidosis, hyperammonaemia (1,089 μmol/l), ketonuria and urinary methylmalonic acids. Emergency treatment included discontinuing protein feeds, providing high calories, carnitine and hydroxocobalamin. NCG 200 mg given at 0 and 90 min decreased plasma ammonia dramatically from 1,089 to 567 µmol/l at 90 min and further to 236 µmol/l at 6 h. Normalisation of ammonia was achieved at 12 h with two further doses of NCG 100 mg. This allowed for early re-institution of feeds at 14 h, followed by metabolic stabilization and recovery. Due to the effectiveness of NCG in this case, the use of the more invasive conventional ammonia-lowering therapeutic options could be avoided.
© 2016 S. Karger AG, Basel.
Similar articles
-
N-carbamylglutamate in emergency management of hyperammonemia in neonatal acute onset propionic and methylmalonic aciduria.Neonatology. 2010;97(3):286-90. doi: 10.1159/000255168. Epub 2009 Nov 4. Neonatology. 2010. PMID: 19887858
-
N-carbamylglutamate enhances ammonia detoxification in a patient with decompensated methylmalonic aciduria.Mol Genet Metab. 2003 Aug;79(4):303-4. doi: 10.1016/s1096-7192(03)00095-7. Mol Genet Metab. 2003. PMID: 12948747
-
N-carbamylglutamate for neonatal hyperammonaemia in propionic acidaemia.J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S219-22. doi: 10.1007/s10545-008-0777-1. Epub 2008 Feb 21. J Inherit Metab Dis. 2008. PMID: 18338235
-
Hyperammonaemia in classic organic acidaemias: a review of the literature and two case histories.Orphanet J Rare Dis. 2018 Dec 6;13(1):219. doi: 10.1186/s13023-018-0963-7. Orphanet J Rare Dis. 2018. PMID: 30522498 Free PMC article. Review.
-
Role of carglumic acid in the long-term management of propionic and methylmalonic acidurias.Orphanet J Rare Dis. 2024 Dec 18;19(1):464. doi: 10.1186/s13023-024-03468-4. Orphanet J Rare Dis. 2024. PMID: 39695809 Free PMC article. Review.
Cited by
-
Urinary Metabolomic Approach Provides New Insights into Distinct Metabolic Profiles of Glutamine and N-Carbamylglutamate Supplementation in Rats.Nutrients. 2016 Aug 4;8(8):478. doi: 10.3390/nu8080478. Nutrients. 2016. PMID: 27527211 Free PMC article.
-
Efficacy of N-carbamoyl-L-glutamic acid for the treatment of inherited metabolic disorders.Expert Rev Endocrinol Metab. 2016;11(6):467-473. doi: 10.1080/17446651.2016.1239526. Epub 2016 Sep 28. Expert Rev Endocrinol Metab. 2016. PMID: 30034506 Free PMC article.
-
Precision medicine in rare disease: Mechanisms of disparate effects of N-carbamyl-l-glutamate on mutant CPS1 enzymes.Mol Genet Metab. 2017 Mar;120(3):198-206. doi: 10.1016/j.ymgme.2016.12.002. Epub 2016 Dec 8. Mol Genet Metab. 2017. PMID: 28007335 Free PMC article.
-
Conducting an investigator-initiated randomized double-blinded intervention trial in acute decompensation of inborn errors of metabolism: Lessons from the N-Carbamylglutamate Consortium.Transl Sci Rare Dis. 2018 Dec 20;3(3-4):157-170. doi: 10.3233/TRD-180031. Transl Sci Rare Dis. 2018. PMID: 30613471 Free PMC article.
-
Presentation and management of N-acetylglutamate synthase deficiency: a review of the literature.Orphanet J Rare Dis. 2020 Oct 9;15(1):279. doi: 10.1186/s13023-020-01560-z. Orphanet J Rare Dis. 2020. PMID: 33036647 Free PMC article.
Publication types
MeSH terms
Substances
Supplementary concepts
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical