Page last updated: 2024-10-16

ammonium hydroxide and Acidemia Propionic

ammonium hydroxide has been researched along with Acidemia Propionic in 14 studies

azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.

Research Excerpts

ExcerptRelevanceReference
"The objective of this study was to determine whether N-carbamylglutamate (NCG) reduces plasma levels of ammonia and glutamine and increases the rate of ureagenesis in patients with propionic acidemia (PA)."9.14N-carbamylglutamate augments ureagenesis and reduces ammonia and glutamine in propionic acidemia. ( Ah Mew, N; Daikhin, Y; McCarter, R; Nissim, I; Tuchman, M; Yudkoff, M, 2010)
"In propionic aciduria and methylmalonic aciduria, hyperammonemia as a symptom of metabolic decompensation is one of the major clinical problems."7.76N-carbamylglutamate in emergency management of hyperammonemia in neonatal acute onset propionic and methylmalonic aciduria. ( Donati, MA; Filippi, L; Fiorini, P; Gozzini, E; la Marca, G; Malvagia, S, 2010)
"5mEq/kg per day), or ornithine α-ketoglutarate (400mg/kg per day) (anaplerotic agents that could fill up the citric acid cycle) would affect plasma levels of glutamine and ammonia, the urinary excretion of Krebs cycle intermediates, and the clinical outcome in 3 patients with propionic acidemia."5.24Anaplerotic therapy in propionic acidemia. ( Bailey, C; Cantor, NL; Ernst, SL; Gappmaier, E; Longo, N; Pasquali, M; Price, LB, 2017)
"The objective of this study was to determine whether N-carbamylglutamate (NCG) reduces plasma levels of ammonia and glutamine and increases the rate of ureagenesis in patients with propionic acidemia (PA)."5.14N-carbamylglutamate augments ureagenesis and reduces ammonia and glutamine in propionic acidemia. ( Ah Mew, N; Daikhin, Y; McCarter, R; Nissim, I; Tuchman, M; Yudkoff, M, 2010)
"Life-threatening hyperammonemia occurs in both inherited and acquired liver diseases affecting ureagenesis, the main pathway for detoxification of neurotoxic ammonia in mammals."4.12O-GlcNAcylation enhances CPS1 catalytic efficiency for ammonia and promotes ureagenesis. ( Arena, P; Attanasio, S; Boffa, I; Brunetti-Pierri, N; Cuomo, P; D'Alessio, AM; De Angelis, A; Desviat, LR; Ferenbach, AT; Häberle, J; Lipshutz, GS; Makris, G; Martínez-Pizarro, A; Motta, A; Nitzahn, M; Nusco, E; Paris, D; Pravata, VM; Richard, E; Rüfenacht, V; Soria, LR; van Aalten, DMF, 2022)
"In propionic aciduria and methylmalonic aciduria, hyperammonemia as a symptom of metabolic decompensation is one of the major clinical problems."3.76N-carbamylglutamate in emergency management of hyperammonemia in neonatal acute onset propionic and methylmalonic aciduria. ( Donati, MA; Filippi, L; Fiorini, P; Gozzini, E; la Marca, G; Malvagia, S, 2010)
"Isovaleric aciduria (IVA), propionic aciduria (PA) and methylmalonic aciduria (MMA) are inherited organic acidurias (OAs) in which impaired organic acid metabolism induces hyperammonaemia arising partly from secondary deficiency of N-acetylglutamate (NAG) synthase."2.82Carglumic acid enhances rapid ammonia detoxification in classical organic acidurias with a favourable risk-benefit profile: a retrospective observational study. ( Baruteau, J; Cano, A; Chakrapani, A; Coker, M; Couce, ML; Del Toro, M; Delgado, MB; Donati, MA; Garcia-Cazorla, A; Gil-Ortega, D; Gomez-de Quero, P; Guffon, N; Hofstede, FC; Kalkan-Ucar, S; Lama-More, R; Le Mouhaer, J; Martinez-Pardo Casanova, M; Molina, A; Papadia, F; Pichard, S; Plisson, C; Rosello, P; Valayannopoulos, V, 2016)
"Propionic acidemia is an inborn error of metabolism caused by a deficiency in the mitochondrial enzyme propionyl-CoA carboxylase that converts the propionyl CoA to methyl malonyl CoA."1.72Interorgan amino acid interchange in propionic acidemia: the missing key to understanding its physiopathology. ( Arrieta, F; Belanger-Quintana, A; Del Valle, M; Fernandez-Felix, BM; Garcia, F; Martinez-Pardo, M; Ruiz-Sala, P; Stanescu, S, 2022)
"Carglumic acid was well tolerated with no side effects noted."1.39Use of carglumic acid in the treatment of hyperammonaemia during metabolic decompensation of patients with propionic acidaemia. ( Abacan, M; Boneh, A, 2013)

Research

Studies (14)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (7.14)29.6817
2010's11 (78.57)24.3611
2020's2 (14.29)2.80

Authors

AuthorsStudies
Stanescu, S1
Belanger-Quintana, A1
Fernandez-Felix, BM1
Ruiz-Sala, P1
Del Valle, M1
Garcia, F1
Arrieta, F1
Martinez-Pardo, M1
Soria, LR1
Makris, G1
D'Alessio, AM1
De Angelis, A1
Boffa, I1
Pravata, VM1
Rüfenacht, V1
Attanasio, S1
Nusco, E1
Arena, P1
Ferenbach, AT1
Paris, D1
Cuomo, P1
Motta, A1
Nitzahn, M1
Lipshutz, GS1
Martínez-Pizarro, A1
Richard, E1
Desviat, LR1
Häberle, J2
van Aalten, DMF1
Brunetti-Pierri, N1
Longo, N2
Price, LB1
Gappmaier, E1
Cantor, NL1
Ernst, SL1
Bailey, C1
Pasquali, M1
Chakrapani, A2
Ah Mew, N2
Item, CB1
Schanzer, A1
Metz, T1
Greber-Platzer, S1
Lischka, J1
Abacan, M1
Boneh, A1
Zwickler, T1
Riderer, A1
Haege, G1
Hoffmann, GF1
Kölker, S1
Burgard, P1
Chapman, KA1
Collado, MS1
Figler, RA1
Hoang, SA1
Armstrong, AJ1
Cui, W1
Purdy, M1
Simmers, MB1
Yazigi, NA1
Summar, ML1
Wamhoff, BR1
Dash, A1
Valayannopoulos, V1
Baruteau, J1
Delgado, MB1
Cano, A1
Couce, ML1
Del Toro, M1
Donati, MA2
Garcia-Cazorla, A1
Gil-Ortega, D1
Gomez-de Quero, P1
Guffon, N1
Hofstede, FC1
Kalkan-Ucar, S1
Coker, M1
Lama-More, R1
Martinez-Pardo Casanova, M1
Molina, A1
Pichard, S1
Papadia, F1
Rosello, P1
Plisson, C1
Le Mouhaer, J1
Schwahn, BC1
Pieterse, L1
Bisset, WM1
Galloway, PG1
Robinson, PH1
Filippi, L1
Gozzini, E1
Fiorini, P1
Malvagia, S1
la Marca, G1
McCarter, R1
Daikhin, Y1
Nissim, I1
Yudkoff, M1
Tuchman, M1
Scholl-Bürgi, S1
Sass, JO1
Zschocke, J1
Karall, D1
Jones, S1
Reed, CA1
Vijay, S1
Walter, JH1
Morris, AA1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Safety & Efficacy of Investigational Products: Ornithine Alpha-ketoglutarate, Glutamine, or Disodium Citrate on Hyperammonemia in Propionic Acidemia.[NCT00645879]Phase 13 participants (Actual)Interventional2008-07-31Completed
Increasing Ureagenesis in Inborn Errors of Metabolism With N-Carbamylglutamate[NCT01341379]Phase 20 participants (Actual)Interventional2010-12-31Withdrawn (stopped due to Lack of funding)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

2 reviews available for ammonium hydroxide and Acidemia Propionic

ArticleYear
Hyperammonaemia in classic organic acidaemias: a review of the literature and two case histories.
    Orphanet journal of rare diseases, 2018, 12-06, Volume: 13, Issue:1

    Topics: Ammonia; Glucose; Glutamates; Humans; Hyperammonemia; Propionic Acidemia

2018
Amino acid metabolism in patients with propionic acidaemia.
    Journal of inherited metabolic disease, 2012, Volume: 35, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids, Branched-Chain; Ammonia; Citric Acid Cycle; Diet;

2012

Trials

3 trials available for ammonium hydroxide and Acidemia Propionic

ArticleYear
Anaplerotic therapy in propionic acidemia.
    Molecular genetics and metabolism, 2017, Volume: 122, Issue:1-2

    Topics: Amino Acids; Ammonia; Carbon-Carbon Ligases; Child; Child, Preschool; Citrates; Citric Acid; Citric

2017
Carglumic acid enhances rapid ammonia detoxification in classical organic acidurias with a favourable risk-benefit profile: a retrospective observational study.
    Orphanet journal of rare diseases, 2016, Mar-31, Volume: 11

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Female; Glutamates; Humans; Hyperammonemia; Infant, N

2016
N-carbamylglutamate augments ureagenesis and reduces ammonia and glutamine in propionic acidemia.
    Pediatrics, 2010, Volume: 126, Issue:1

    Topics: Administration, Oral; Adolescent; Ammonia; Blood Chemical Analysis; Child; Child, Preschool; Confide

2010

Other Studies

9 other studies available for ammonium hydroxide and Acidemia Propionic

ArticleYear
Interorgan amino acid interchange in propionic acidemia: the missing key to understanding its physiopathology.
    Amino acids, 2022, Volume: 54, Issue:5

    Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Glutamine; Humans; Hyperammonem

2022
O-GlcNAcylation enhances CPS1 catalytic efficiency for ammonia and promotes ureagenesis.
    Nature communications, 2022, 09-05, Volume: 13, Issue:1

    Topics: Acetylglucosamine; Ammonia; Animals; Biocatalysis; Carbamoyl-Phosphate Synthase (Ammonia); Disease M

2022
Demethylation of the hypoxia induction factor 1 binding site of GPX3 at excess blood ammonia in propionic acidemia.
    Clinical biochemistry, 2019, Volume: 66

    Topics: Ammonia; Binding Sites; Demethylation; DNA Methylation; Glutathione Peroxidase; Humans; Hyperammonem

2019
Use of carglumic acid in the treatment of hyperammonaemia during metabolic decompensation of patients with propionic acidaemia.
    Molecular genetics and metabolism, 2013, Volume: 109, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Carnitine; Child, Preschool; Female; Glutamates; Huma

2013
Usefulness of biochemical parameters in decision-making on the start of emergency treatment in patients with propionic acidemia.
    Journal of inherited metabolic disease, 2014, Volume: 37, Issue:1

    Topics: Acid-Base Equilibrium; Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Ammonia; Appetite; C

2014
Recapitulation of metabolic defects in a model of propionic acidemia using patient-derived primary hepatocytes.
    Molecular genetics and metabolism, 2016, Volume: 117, Issue:3

    Topics: Actins; Amino Acids, Branched-Chain; Ammonia; Carbon-Carbon Ligases; Cells, Cultured; Child; Fibrobl

2016
Biochemical efficacy of N-carbamylglutamate in neonatal severe hyperammonaemia due to propionic acidaemia.
    European journal of pediatrics, 2010, Volume: 169, Issue:1

    Topics: Ammonia; Dose-Response Relationship, Drug; Female; Follow-Up Studies; Glutamates; Humans; Hyperammon

2010
N-carbamylglutamate in emergency management of hyperammonemia in neonatal acute onset propionic and methylmalonic aciduria.
    Neonatology, 2010, Volume: 97, Issue:3

    Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Ammonia; Emergency Medical Services; Female; Gl

2010
N-carbamylglutamate for neonatal hyperammonaemia in propionic acidaemia.
    Journal of inherited metabolic disease, 2008, Volume: 31 Suppl 2

    Topics: Ammonia; Biomarkers; Female; Glutamates; Humans; Hyperammonemia; Infant, Newborn; Intubation, Gastro

2008