Impact of Fruit and Vegetable Protein vs. Milk Protein on Metabolic Control of Children with Phenylketonuria: A Randomized Crossover Controlled Trial.

fruits metabolic control milk protein phenylalanine phenylketonuria vegetables

Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
13 Oct 2022
Historique:
received: 21 09 2022
revised: 07 10 2022
accepted: 08 10 2022
entrez: 27 10 2022
pubmed: 28 10 2022
medline: 29 10 2022
Statut: epublish

Résumé

Fruits and vegetables containing phenylalanine ≤ 75 mg/100 g (except potatoes) have little impact on blood phenylalanine in phenylketonuria (PKU). In a randomized, controlled, crossover intervention trial, we examined the effect of increasing phenylalanine intake from fruits and vegetables, containing phenylalanine 76−100 mg /100 g, compared with milk protein sources on blood phenylalanine control. This was a five-phase study (4 weeks each phase). In Phase A, patients remained on their usual diet and then were randomly allocated to start Phase B and C (an additional phenylalanine intake of 50 mg/day, then 100 mg from fruits and vegetables containing phenylalanine 76−100 mg/100 g) or Phase D and E (an additional phenylalanine intake of 50 mg/day then 100 mg/day from milk sources). There was a 7-day washout with the usual phenylalanine-restricted diet between Phase B/C and D/E. Blood phenylalanine was measured on the last 3 days of each week. If four out of six consecutive blood phenylalanine levels were >360 μmol/L in one arm, this intervention was stopped. Sixteen patients (median age 10.5 y; range 6−12 y) were recruited. At baseline, a median of 6 g/day (range: 3−25) natural protein and 60 g/day (range: 60−80) protein equivalent from protein substitute were prescribed. Median phenylalanine levels were: Phase A—240 μmol/L; Phase B—260 μmol/L; Phase C—280 μmol/L; Phase D—270 μmol/L and Phase E—280 μmol/L. All patients tolerated an extra 50 mg/day of phenylalanine from fruit and vegetables, containing phenylalanine 76−100 mg/100 g, but only 11/16 (69%) tolerated an additional 100 mg /day. With milk protein, only 8/16 (50%) tolerated an extra 50 mg/day and only 5/16 (31%) tolerated an additional 100 mg/day of phenylalanine. Tolerance was defined as maintaining consistent blood phenylalanine levels < 360 μmol/L throughout each study arm. There was a trend that vegetable protein had less impact on blood phenylalanine control than milk protein, but overall, the differences were not statistically significant (p = 0.152). This evidence supports the PKU European Guidelines cutoff that fruit and vegetables containing 76−100 mg phenylalanine/100 g should be calculated as part of the phenylalanine exchange system. Tolerance of the ‘free use’ of these fruits and vegetables depends on inter-patient variability but cannot be recommended for all patients with PKU.

Identifiants

pubmed: 36296952
pii: nu14204268
doi: 10.3390/nu14204268
pmc: PMC9611310
pii:
doi:

Substances chimiques

Plant Proteins, Dietary 0
Milk Proteins 0
Phenylalanine 47E5O17Y3R

Types de publication

Randomized Controlled Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : National Society for Phenylketonuria (NSPKU) grant

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Auteurs

Alex Pinto (A)

Dietetic Department, Birmingham Women's and Children's Hospital, Birmingham B4 6NH, UK.
Faculty of Health, Plymouth Institute of Health and Care Research, University of Plymouth, Plymouth PL6 8BH, UK.

Anne Daly (A)

Dietetic Department, Birmingham Women's and Children's Hospital, Birmingham B4 6NH, UK.

Júlio César Rocha (JC)

NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade Nova de Lisboa, 1169-056 Lisboa, Portugal.
CINTESIS, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade Nova de Lisboa, 1169-056 Lisboa, Portugal.
Reference Centre of Inherited Metabolic Diseases, Centro Hospitalar Universitario de Lisboa Central, 1169-045 Lisboa, Portugal.

Catherine Ashmore (C)

Dietetic Department, Birmingham Women's and Children's Hospital, Birmingham B4 6NH, UK.

Sharon Evans (S)

Dietetic Department, Birmingham Women's and Children's Hospital, Birmingham B4 6NH, UK.

Richard Jackson (R)

Cancer Research UK Liverpool Cancer Trials Unit, University of Liverpool, Liverpool L69 3GL, UK.

Anne Payne (A)

Faculty of Health, Plymouth Institute of Health and Care Research, University of Plymouth, Plymouth PL6 8BH, UK.

Mary Hickson (M)

Faculty of Health, Plymouth Institute of Health and Care Research, University of Plymouth, Plymouth PL6 8BH, UK.

Anita MacDonald (A)

Dietetic Department, Birmingham Women's and Children's Hospital, Birmingham B4 6NH, UK.
Faculty of Health, Plymouth Institute of Health and Care Research, University of Plymouth, Plymouth PL6 8BH, UK.

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