Uniformity of Food Protein Interpretation Amongst Dietitians for Patients with Phenylketonuria (PKU): 2020 UK National Consensus Statements.
Delphi method
Phe
consensus
exchanges
food labelling
phenylalanine
phenylketonuria (PKU)
protein
Journal
Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595
Informations de publication
Date de publication:
24 Jul 2020
24 Jul 2020
Historique:
received:
17
06
2020
revised:
15
07
2020
accepted:
22
07
2020
entrez:
30
7
2020
pubmed:
30
7
2020
medline:
13
3
2021
Statut:
epublish
Résumé
In phenylketonuria (PKU), variable dietary advice provided by health professionals and social media leads to uncertainty for patients/caregivers reliant on accurate, evidence based dietary information. Over four years, 112 consensus statements concerning the allocation of foods in a low phenylalanine diet for PKU were developed by the British Inherited Metabolic Disease Dietitians Group (BIMDG-DG) from 34 PKU treatment centres, utilising 10 rounds of Delphi consultation to gain a majority (≥75%) decision. A mean of 29 UK dietitians (range: 18-40) and 18 treatment centres (range: 13-23) contributed in each round. Statements encompassed all foods/food groups divided into four categories based on defined protein/phenylalanine content: (1) foods high in protein/phenylalanine (best avoided); (2) foods allowed without restriction including fruit/vegetables containing phenylalanine ≤75 mg/100 g and most foods containing protein ≤0.5 g/100 g; (3) foods that should be calculated/weighed as an exchange food if they contain protein exchange ingredients (categorized into foods with a protein content of: >0.1 g/100 g (milk/plant milks only), >0.5 g/100 g (bread/pasta/cereal/flours), >1 g/100 g (cook-in/table-top sauces/dressings), >1.5 g/100 g (soya sauces)); and (4) fruit/vegetables containing phenylalanine >75 mg/100 g allocated as part of the protein/phenylalanine exchange system. These statements have been endorsed and translated into practical dietary management advice by the medical advisory dietitians for the National Society for PKU (NSPKU).
Identifiants
pubmed: 32722073
pii: nu12082205
doi: 10.3390/nu12082205
pmc: PMC7468820
pii:
doi:
Substances chimiques
Dietary Proteins
0
Phenylalanine
47E5O17Y3R
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Références
J Inherit Metab Dis. 2003;26(4):327-38
pubmed: 12971420
Clin Nutr. 2009 Jun;28(3):231-6
pubmed: 19362397
Mol Genet Metab Rep. 2018 Nov 25;18:39-44
pubmed: 30705824
Mol Genet Metab Rep. 2015 Oct 22;5:36-41
pubmed: 28649540
Orphanet J Rare Dis. 2017 Oct 12;12(1):162
pubmed: 29025426
J Hum Nutr Diet. 2006 Jun;19(3):229-36
pubmed: 16756538
Eur J Clin Nutr. 2012 May;66(5):633-8
pubmed: 22318648
J Nutr Metab. 2017;2017:4083293
pubmed: 29057118
Orphanet J Rare Dis. 2019 Jan 3;14(1):2
pubmed: 30606267
Mol Genet Metab. 2012 Jul;106(3):264-8
pubmed: 22607939
Arch Dis Child. 1993 Mar;68(3):426-7
pubmed: 8466250
Genet Med. 2014 Feb;16(2):121-31
pubmed: 24385075
Nutrients. 2020 Jun 25;12(6):
pubmed: 32630585
Mol Genet Metab Rep. 2018 Oct 18;17:57-63
pubmed: 30364670
Eur J Clin Nutr. 2014 Mar;68(3):401-3
pubmed: 24398645
Orphanet J Rare Dis. 2020 Jun 30;15(1):171
pubmed: 32605583