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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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Date

2019-11-26

Authors

Molema, Femke
Gleich, Florian
Burgard, Peter
van-der-Ploeg, Ans T
Summar, Marshall L
Chapman, Kimberly A
Baric, Ivo
Lund, Allan M
Kölker, Stefan
Williams, Monique

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Wiley
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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.

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MeSH Terms

Adolescent
Adult
Amino Acid Metabolism, Inborn Errors
Amino Acids
Child
Child, Preschool
Cross-Sectional Studies
Dietary Supplements
Europe
Feasibility Studies
Female
Humans
Hyperammonemia
Infant
Male
Ornithine
Propionic Acidemia
Registries
Retrospective Studies
Treatment Outcome
Urea Cycle Disorders, Inborn
Young Adult

DeCS Terms

Aminoácidos
Metabolismo
Enfermedades Metabólicas
Urea
Ingesta Diaria Recomendada
Ligasas
Hiperamonemia

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Keywords

L-citrulline and L-arginine, amino acid mixtures, branched-chain amino acids, dietary and supplemental treatment, organic acidurias, urea-cycle disorders

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 Inherit Metab Dis. 2019 Nov;42(6):1162-1175