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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.

dc.contributor.authorMolema, Femke
dc.contributor.authorGleich, Florian
dc.contributor.authorBurgard, Peter
dc.contributor.authorvan-der-Ploeg, Ans T
dc.contributor.authorSummar, Marshall L
dc.contributor.authorChapman, Kimberly A
dc.contributor.authorBaric, Ivo
dc.contributor.authorLund, Allan M
dc.contributor.authorKölker, Stefan
dc.contributor.authorWilliams, Monique
dc.contributor.funderErasmus University Medical Cente
dc.contributor.groupAdditional individual contributors from E-IMD
dc.date.accessioned2023-01-25T10:30:28Z
dc.date.available2023-01-25T10:30:28Z
dc.date.issued2019-11-26
dc.description.abstractOrganic 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.description.versionSi
dc.identifier.citationMolema 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 Inherit Metab Dis. 2019 Nov;42(6):1162-1175
dc.identifier.doi10.1002/jimd.12066
dc.identifier.essn1573-2665
dc.identifier.pmid30734935
dc.identifier.unpaywallURLhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/jimd.12066
dc.identifier.urihttp://hdl.handle.net/10668/13535
dc.issue.number6
dc.journal.titleJournal of inherited metabolic disease
dc.journal.titleabbreviationJ Inherit Metab Dis
dc.language.isoen
dc.organizationHospital Universitario Regional de Málaga
dc.page.number1162-1175
dc.provenanceRealizada la curación de contenido 01/04/2025
dc.publisherWiley
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.relation.projectID2015-061
dc.relation.publisherversionhttps://doi.org/10.1002/jimd.12066
dc.rightsAttribution-NonCommercial 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subjectL-citrulline and L-arginine
dc.subjectamino acid mixtures
dc.subjectbranched-chain amino acids
dc.subjectdietary and supplemental treatment
dc.subjectorganic acidurias
dc.subjecturea-cycle disorders
dc.subject.decsAminoácidos
dc.subject.decsMetabolismo
dc.subject.decsEnfermedades Metabólicas
dc.subject.decsUrea
dc.subject.decsIngesta Diaria Recomendada
dc.subject.decsLigasas
dc.subject.decsHiperamonemia
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshAmino Acid Metabolism, Inborn Errors
dc.subject.meshAmino Acids
dc.subject.meshChild
dc.subject.meshChild, Preschool
dc.subject.meshCross-Sectional Studies
dc.subject.meshDietary Supplements
dc.subject.meshEurope
dc.subject.meshFeasibility Studies
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshHyperammonemia
dc.subject.meshInfant
dc.subject.meshMale
dc.subject.meshOrnithine
dc.subject.meshPropionic Acidemia
dc.subject.meshRegistries
dc.subject.meshRetrospective Studies
dc.subject.meshTreatment Outcome
dc.subject.meshUrea Cycle Disorders, Inborn
dc.subject.meshYoung Adult
dc.titleEvaluation 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.typeresearch article
dc.type.hasVersionVoR
dc.volume.number42
dspace.entity.typePublication

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