Literature DB >> 30734935

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.

Femke Molema1, Florian Gleich2, Peter Burgard2, Ans T van der Ploeg1, Marshall L Summar3, Kimberly A Chapman3, Ivo Barić4, Allan M Lund5, Stefan Kölker2, Monique Williams1.   

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.
© 2019 The Authors. Journal of Inherited Metabolic Disease published by John Wiley & Sons Ltd on behalf of SSIEM.

Entities:  

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

Mesh:

Substances:

Year:  2019        PMID: 30734935     DOI: 10.1002/jimd.12066

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  9 in total

1.  Protection of Cystinotic Mice by Kidney-Specific Megalin Ablation Supports an Endocytosis-Based Mechanism for Nephropathic Cystinosis Progression.

Authors:  Virginie Janssens; Héloïse P Gaide Chevronnay; Sandrine Marie; Marie-Françoise Vincent; Patrick Van Der Smissen; Nathalie Nevo; Seppo Vainio; Rikke Nielsen; Erik I Christensen; François Jouret; Corinne Antignac; Christophe E Pierreux; Pierre J Courtoy
Journal:  J Am Soc Nephrol       Date:  2019-09-23       Impact factor: 10.121

2.  Severe anemia in patients with Propionic acidemia is associated with branched-chain amino acid imbalance.

Authors:  Sinziana Stanescu; Amaya Belanger-Quintana; Borja Manuel Fernandez-Felix; Francisco Arrieta; Victor Quintero; Maria Soledad Maldonado; Patricia Alcaide; Mercedes Martínez-Pardo
Journal:  Orphanet J Rare Dis       Date:  2021-05-18       Impact factor: 4.123

3.  Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision.

Authors:  Patrick Forny; Friederike Hörster; Diana Ballhausen; Anupam Chakrapani; Kimberly A Chapman; Carlo Dionisi-Vici; Marjorie Dixon; Sarah C Grünert; Stephanie Grunewald; Goknur Haliloglu; Michel Hochuli; Tomas Honzik; Daniela Karall; Diego Martinelli; Femke Molema; Jörn Oliver Sass; Sabine Scholl-Bürgi; Galit Tal; Monique Williams; Martina Huemer; Matthias R Baumgartner
Journal:  J Inherit Metab Dis       Date:  2021-03-09       Impact factor: 4.750

4.  Amino Acid Plasma Profiles from a Prolonged-Release Protein Substitute for Phenylketonuria: A Randomized, Single-Dose, Four-Way Crossover Trial in Healthy Volunteers.

Authors:  Mika Scheinin; Anna Barassi; Jouni Junnila; Zsófia Lovró; Giorgio Reiner; Essi Sarkkinen; Anita MacDonald
Journal:  Nutrients       Date:  2020-06-02       Impact factor: 5.717

5.  Dietary management and growth outcomes in children with propionic acidemia: A natural history study.

Authors:  Haneen Saleemani; Csilla Egri; Gabriella Horvath; Sylvia Stockler-Ipsiroglu; Rajavel Elango
Journal:  JIMD Rep       Date:  2021-06-14

Review 6.  Rare Disease Registries Are Key to Evidence-Based Personalized Medicine: Highlighting the European Experience.

Authors:  Stefan Kölker; Florian Gleich; Ulrike Mütze; Thomas Opladen
Journal:  Front Endocrinol (Lausanne)       Date:  2022-03-04       Impact factor: 5.555

7.  Monitoring Methylmalonic Aciduria by NMR Urinomics.

Authors:  Alina Nicolescu; Daniela Blanita; Chiril Boiciuc; Victoria Hlistun; Mihaela Cristea; Dorina Rotaru; Ludmila Pinzari; Ana Oglinda; Adela Stamati; Isabela Tarcomnicu; Andreea Tutulan-Cunita; Danae Stambouli; Sergiu Gladun; Ninel Revenco; Natalia Uşurelu; Calin Deleanu
Journal:  Molecules       Date:  2020-11-14       Impact factor: 4.411

8.  Homocystinuria patient and caregiver survey: experiences of diagnosis and patient satisfaction.

Authors:  M Huemer; A A M Morris; T Morrison; F Bösch; M A Landolt; V Kožich
Journal:  Orphanet J Rare Dis       Date:  2021-03-10       Impact factor: 4.123

9.  Anthropometrics, Dietary Intake and Body Composition in Urea Cycle Disorders and Branched Chain Organic Acidemias: A Case Study of 18 Adults on Low-Protein Diets.

Authors:  Giorgia Gugelmo; Livia Lenzini; Francesco Francini-Pesenti; Ilaria Fasan; Paolo Spinella; Romina Valentini; Angela Miraval; Angelo Avogaro; Nicola Vitturi
Journal:  Nutrients       Date:  2022-01-21       Impact factor: 5.717

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.