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Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry

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dc.contributor.author Molema, Femke
dc.contributor.author Gleich, Florian
dc.contributor.author Burgard, Peter
dc.contributor.author van-der-Ploeg, Ans-T
dc.contributor.author Summar, Marshall-L
dc.contributor.author Chapman, Kimberly-A
dc.contributor.author Baric, Ivo
dc.contributor.author Lund, Allan-M
dc.contributor.author Koelker, Stefan
dc.contributor.author Williams, Monique
dc.contributor.author Hoerster, F
dc.contributor.author Jelsig, A-M
dc.contributor.author de-Lonlay, P
dc.contributor.author Wijburg, F-A
dc.contributor.author Bosch, A
dc.contributor.author Freisinger, P
dc.contributor.author Posset, R
dc.contributor.author Augoustides-Savvopoulou, P
dc.contributor.author Avram, P
dc.contributor.author Deleanu, C
dc.contributor.author Baumgartner, M-R
dc.contributor.author Haberle, J
dc.contributor.author Blasco-Alonso, J
dc.contributor.author Burlina, A-B
dc.contributor.author Rubert, L
dc.contributor.author García-Cazorla, A
dc.contributor.author Cortes-i-Saladelafont, E
dc.contributor.author Dionisi-Vici, C
dc.contributor.author Martinelli, D
dc.contributor.author Dobbelaere, D
dc.contributor.author Mention, K
dc.contributor.author Grunewald, S
dc.contributor.author Chakrapani, A
dc.contributor.author Hwu, W--L
dc.contributor.author Chien, Y--H
dc.contributor.author Lee, N--C
dc.contributor.author Karall, D
dc.contributor.author Scholl-Buergi, S
dc.contributor.author Lachmann, R
dc.contributor.author De-Laet, C
dc.contributor.author Matsumoto, S
dc.contributor.author de-Meirleir, L
dc.contributor.author Muehlhausen, C
dc.contributor.author Schiff, M
dc.contributor.author Peña-Quintana, L
dc.contributor.author Djordjevic, M
dc.contributor.author Sarajlija, A
dc.contributor.author Sykut-Cegielska, J
dc.contributor.author Wisniewska, A
dc.contributor.author Leao-Teles, E
dc.contributor.author Alves, S
dc.contributor.author Vara, R
dc.contributor.author Vives-Piñera, Inmaculada
dc.contributor.author Ortega, D-G
dc.contributor.author Morris, A
dc.contributor.author Zeman, J
dc.contributor.author Honzik, T
dc.contributor.author Chabrol, B
dc.contributor.author Arnaudo, F
dc.contributor.author Cano, A
dc.contributor.author Thompson, N
dc.contributor.author Eyskens, F
dc.contributor.author Lindner, M
dc.contributor.author Luesebrink, N
dc.contributor.author Jalan, A
dc.contributor.author Sokal, E
dc.contributor.author Legros, V
dc.contributor.author Nassogne, M-C
dc.date.accessioned 2026-02-12T12:13:49Z
dc.date.available 2026-02-12T12:13:49Z
dc.date.issued 2019-11
dc.identifier.citation Molema F, Gleich F, Burgard P, Van Der Ploeg AT, Summar ML, Chapman KA, et al. Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry. J of Inher Metab Disea. noviembre de 2019;42(6):1162-75.
dc.identifier.issn 0141-8955
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/24369
dc.description.abstract Organic acidurias (OAD) and urea-cycle disorders (UCD) are rare inherited disorders affecting amino acid and protein metabolism. As dietary practice varies widely, we assessed their long-term prescribed dietary treatment against published guideline and studied plasma amino acids levels. We analyzed data from the first visit recorded in the European registry and network for intoxication type metabolic diseases (E-IMD, Chafea no. 2010 12 01). In total, 271 methylmalonic aciduria (MMA) and propionic aciduria (PA) and 361 UCD patients were included. Median natural protein prescription was consistent with the recommended daily allowance (RDA), plasma L-valine (57%), and L-isoleucine (55%) levels in MMA and PA lay below reference ranges. Plasma levels were particularly low in patients who received amino acid mixtures (AAMs-OAD) and L-isoleucine:L-leucine:L-valine (BCAA) ratio was 1.0:3.0:3.2. In UCD patients, plasma L-valine, L-isoleucine, and L-leucine levels lay below reference ranges in 18%, 30%, and 31%, respectively. In symptomatic UCD patients who received AAM-UCD, the median natural protein prescription lay below RDA, while their L-valine and L-isoleucine levels and plasma BCAA ratios were comparable to those in patients who did not receive AAM-UCD. Notably, in patients with ornithine transcarbamylase syndrome (OTC-D), carbamylphosphate synthetase 1 syndrome (CPS1-D) and hyperammonemia-hyperornithinemia-homocitrullinemia (HHH) syndrome selective L-citrulline supplementation resulted in higher plasma L-arginine levels than selective L-arginine supplementation. In conclusion, while MMA and PA patients who received AAMs-OAD had very low BCAA levels and disturbed plasma BCAA ratios, AAMs-UCD seemed to help UCD patients obtain normal BCAA levels. In patients with OTC-D, CPS1-D, and HHH syndrome, selective L-citrulline seemed preferable to selective L-arginine supplementation.
dc.language.iso eng
dc.publisher WILEY
dc.rights Atribución/Reconocimiento-NoComercial 4.0 Internacional
dc.rights.uri http://creativecommons.org/licenses/by-nc/4.0/ *
dc.subject.mesh Adolescent
dc.subject.mesh Adult
dc.subject.mesh Amino Acid Metabolism, Inborn Errors/diet therapy/epidemiology
dc.subject.mesh Amino Acids/administration & dosage
dc.subject.mesh Child
dc.subject.mesh Child, Preschool
dc.subject.mesh Cross-Sectional Studies
dc.subject.mesh Dietary Supplements
dc.subject.mesh Europe/epidemiology
dc.subject.mesh Feasibility Studies
dc.subject.mesh Female
dc.subject.mesh Humans
dc.subject.mesh Hyperammonemia/diet therapy/epidemiology
dc.subject.mesh Infant
dc.subject.mesh Male
dc.subject.mesh Ornithine/deficiency
dc.subject.mesh Propionic Acidemia/diet therapy/epidemiology
dc.subject.mesh Registries
dc.subject.mesh Retrospective Studies
dc.subject.mesh Treatment Outcome
dc.subject.mesh Urea Cycle Disorders, Inborn/diet therapy/epidemiology
dc.subject.mesh Young Adult
dc.title Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 30734935
dc.relation.publisherversion https://onlinelibrary.wiley.com/doi/10.1002/jimd.12066
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1002/jimd.12066
dc.journal.title Journal of Inherited Metabolic Disease
dc.identifier.essn 1573-2665


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