Literature DB >> 27117930

Protein substitutes for phenylketonuria in Europe: access and nutritional composition.

M J Pena1, M F de Almeida1,2, E van Dam3, K Ahring4, A Bélanger-Quintana5, K Dokoupil6, H Gokmen-Ozel7, A M Lammardo8, A MacDonald9, M Robert10, J C Rocha1,11,12.   

Abstract

BACKGROUND/
OBJECTIVES: Protein substitutes (PS) are an essential component in the dietary management of phenylketonuria (PKU). PS are available as phenylalanine-free amino-acid mixtures (AAM), glycomacropeptide-based PS (GMP) and large neutral amino acids (LNAA). There is a lack of information regarding their availability in different countries and comparison of their nutritional composition is limited. The objectives of this study were to identify the number of PS available in different European countries and Turkey and to compare their nutritional composition. SUBJECTS/
METHODS: Members of the European Nutritionist Expert Panel on PKU (ENEP) (Portugal, Spain, Belgium, Italy, Germany, Netherlands, United Kingdom, Denmark and Turkey) provided data on PS available in each country. The nutritional composition of PS available in Portugal was analyzed.
RESULTS: The number of PS available in each country varied from 30 (Turkey) to 105 (Germany), with a median of 64. GMP was available only in Portugal, whereas LNAA was an option in Portugal, Italy, Turkey and Denmark. Some PS were designed for weaning. Many PS did not contain added fat and fiber. GMP contained the highest carbohydrate (CHO) and energy content as well as higher LNAA content compared with AAM. Only one AAM contained added fructo-oligosaccharides and galacto-oligosaccharides. AAM designed for the first year of life had the highest CHO, fat and LNAA contribution. Liquid AAM had lower CHO and fat contents compared with powdered AAM, but contained higher LNAA.
CONCLUSIONS: There was widely dissimilar numbers of PS available in different countries. Nutritional composition of different PS was variable and should be considered before prescription.

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Year:  2016        PMID: 27117930     DOI: 10.1038/ejcn.2016.54

Source DB:  PubMed          Journal:  Eur J Clin Nutr        ISSN: 0954-3007            Impact factor:   4.016


  36 in total

Review 1.  Weaning infants with phenylketonuria: a review.

Authors:  A MacDonald; S Evans; B Cochrane; J Wildgoose
Journal:  J Hum Nutr Diet       Date:  2011-08-08       Impact factor: 3.089

Review 2.  Micronutrient status in phenylketonuria.

Authors:  M Robert; J C Rocha; M van Rijn; K Ahring; A Bélanger-Quintana; A MacDonald; K Dokoupil; H Gokmen Ozel; A M Lammardo; P Goyens; F Feillet
Journal:  Mol Genet Metab       Date:  2013-09-19       Impact factor: 4.797

Review 3.  Is overweight an issue in phenylketonuria?

Authors:  Júlio C Rocha; Anita MacDonald; Friedrich Trefz
Journal:  Mol Genet Metab       Date:  2013-08-31       Impact factor: 4.797

Review 4.  Oxidative stress in phenylketonuria: future directions.

Authors:  Júlio César Rocha; Maria João Martins
Journal:  J Inherit Metab Dis       Date:  2011-11-25       Impact factor: 4.982

5.  Large neutral amino acids in daily practice.

Authors:  Kirsten Kiær Ahring
Journal:  J Inherit Metab Dis       Date:  2010-03-19       Impact factor: 4.982

Review 6.  Large neutral amino acids supplementation in phenylketonuric patients.

Authors:  J C Rocha; F Martel
Journal:  J Inherit Metab Dis       Date:  2009-05-13       Impact factor: 4.982

Review 7.  New ways of defining protein and energy relationships in inborn errors of metabolism.

Authors:  Maureen Humphrey; Helen Truby; Avihu Boneh
Journal:  Mol Genet Metab       Date:  2014-05-22       Impact factor: 4.797

8.  Early dietary treated patients with phenylketonuria can achieve normal growth and body composition.

Authors:  Júlio C Rocha; Francjan J van Spronsen; Manuela F Almeida; Elisabete Ramos; João T Guimarães; Nuno Borges
Journal:  Mol Genet Metab       Date:  2013-10-22       Impact factor: 4.797

9.  PKU-what is daily practice in various centres in Europe? Data from a questionnaire by the scientific advisory committee of the European Society of Phenylketonuria and Allied Disorders.

Authors:  F J van Spronsen; K Kiaer Ahring; M Gizewska
Journal:  J Inherit Metab Dis       Date:  2009-01-13       Impact factor: 4.982

10.  Double blind placebo control trial of large neutral amino acids in treatment of PKU: effect on blood phenylalanine.

Authors:  R Matalon; K Michals-Matalon; G Bhatia; A B Burlina; A P Burlina; C Braga; L Fiori; M Giovannini; E Grechanina; P Novikov; J Grady; S K Tyring; F Guttler
Journal:  J Inherit Metab Dis       Date:  2007-02-27       Impact factor: 4.750

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  13 in total

1.  Nutritional status in patients with phenylketonuria using glycomacropeptide as their major protein source.

Authors:  A Pinto; M F Almeida; P C Ramos; S Rocha; A Guimas; R Ribeiro; E Martins; A Bandeira; A MacDonald; J C Rocha
Journal:  Eur J Clin Nutr       Date:  2017-04-12       Impact factor: 4.016

2.  Dietary patterns, cost and compliance with low-protein diet of phenylketonuria and other inherited metabolic diseases.

Authors:  T Mlčoch; R Puda; P Ješina; M Lhotáková; Š Štěrbová; T Doležal
Journal:  Eur J Clin Nutr       Date:  2017-06-28       Impact factor: 4.016

3.  Carbohydrate status in patients with phenylketonuria.

Authors:  María L Couce; Paula Sánchez-Pintos; Isidro Vitoria; María-José De Castro; Luís Aldámiz-Echevarría; Patricia Correcher; Ana Fernández-Marmiesse; Iria Roca; Alvaro Hermida; Miguel Martínez-Olmos; Rosaura Leis
Journal:  Orphanet J Rare Dis       Date:  2018-06-27       Impact factor: 4.123

4.  Dietary management of maternal phenylketonuria with glycomacropeptide and amino acids supplements: A case report.

Authors:  A Pinto; M F Almeida; A Cunha; C Carmona; S Rocha; A Guimas; R Ribeiro; C R Mota; E Martins; A MacDonald; J C Rocha
Journal:  Mol Genet Metab Rep       Date:  2017-10-18

5.  Nutrient intake, body composition, and blood phenylalanine control in children with phenylketonuria compared to healthy controls.

Authors:  Melissa Sailer; Gabriela Elizondo; Julie Martin; Cary O Harding; Melanie B Gillingham
Journal:  Mol Genet Metab Rep       Date:  2020-05-11

6.  Reply to Jakovac; Severity of COVID-19 infection in patients with phenylketonuria: is vitamin D status protective?

Authors:  Júlio César Rocha; Conceição Calhau; Anita MacDonald
Journal:  Am J Physiol Endocrinol Metab       Date:  2020-06-01       Impact factor: 4.310

7.  The Use of Glycomacropeptide in Patients with Phenylketonuria: A Systematic Review and Meta-Analysis.

Authors:  Maria João Pena; Alex Pinto; Anne Daly; Anita MacDonald; Luís Azevedo; Júlio César Rocha; Nuno Borges
Journal:  Nutrients       Date:  2018-11-18       Impact factor: 5.717

8.  Long-Term Growth in Phenylketonuria: A Systematic Review and Meta-Analysis.

Authors:  Fatma Ilgaz; Alex Pinto; Hülya Gökmen-Özel; Julio César Rocha; Esther van Dam; Kirsten Ahring; Amaya Bélanger-Quintana; Katharina Dokoupil; Erdem Karabulut; Anita MacDonald
Journal:  Nutrients       Date:  2019-09-03       Impact factor: 5.717

Review 9.  Dietary intervention in the management of phenylketonuria: current perspectives.

Authors:  Júlio César Rocha; Anita MacDonald
Journal:  Pediatric Health Med Ther       Date:  2016-12-01

10.  Optimising amino acid absorption: essential to improve nitrogen balance and metabolic control in phenylketonuria.

Authors:  Anita MacDonald; Rani H Singh; Júlio César Rocha; Francjan J van Spronsen
Journal:  Nutr Res Rev       Date:  2018-10-04       Impact factor: 7.800

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