Literature DB >> 34116943

Nutrition status of adults with phenylketonuria treated with pegvaliase.

Krista Viau1, Ann Wessel2, Leslie Martell2, Stephanie Sacharow3, Fran Rohr4.   

Abstract

BACKGROUND: Pegvaliase is an enzyme substitution therapy that reduces blood phenylalanine (Phe) in adults with phenylketonuria (PKU), and often allows normalization of protein intake (≥0.8 g protein/kg). Here we examine the nutrition status of adults with PKU consuming a normal protein intake without medical food after being treated with pegvaliase for ≥1 year.
METHODS: A cross-sectional study evaluating nutritional intake (3-day food record and food frequency questionnaire), anthropometrics, laboratory indices of protein, micronutrient, and essential fatty acid (EFA) status, and questionnaires evaluating food neophobia and Epicurean eating pleasure.
RESULTS: Participants (n = 18, 61% female) started pegvaliase 4.9 ± 2.1 years prior to enrollment and were aged 38.2 ± 8.8 years with a mean BMI of 29.2 ± 4.1 kg/m2. Participants consumed a mean of 73.2 ± 17.6 g protein/d (1.0 ± 0.3 g/kg/d). Eleven participants had low blood Phe (<30 μmol/L) with adequate protein intake and normal indices of protein status. Micronutrient and EFA concentrations were normal except for mildly low vitamin D (<30 ng/mL, n = 12). Intakes of sodium, saturated fat, and added sugars exceeded recommendations for healthy adults, though mean diet quality was comparable to a US adult reference population. Lower food neophobia scores correlated with an increased aesthetic appreciation of food. However, 53% of participants self-reported having moderate (n = 6) to high (n = 3) food neophobia. DISCUSSION: Participants treated with pegvaliase consumed an unrestricted diet with adequate dietary protein and, overall, had normal protein, micronutrient, and fatty acid status. Despite low blood Phe, protein nutriture was not compromised. While nutritional deficiencies were not identified, diet quality was suboptimal and some participants reported food neophobia. Nutrition education remains an important component of care as patients adapt to a normal diet.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Diet quality; Hypophenylalanemia; Nutrition; Pegvaliase; Phenylketonuria

Mesh:

Substances:

Year:  2021        PMID: 34116943     DOI: 10.1016/j.ymgme.2021.06.002

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  2 in total

Review 1.  The Impact of the Quality of Nutrition and Lifestyle in the Reproductive Years of Women with PKU on the Long-Term Health of Their Children.

Authors:  Maria Inês Gama; Alex Pinto; Anne Daly; Júlio César Rocha; Anita MacDonald
Journal:  Nutrients       Date:  2022-02-28       Impact factor: 5.717

2.  Characterization of Choline Nutriture among Adults and Children with Phenylketonuria.

Authors:  Meriah S Schoen; Usha Ramakrishnan; Jessica A Alvarez; Thomas R Ziegler; Xiangqin Cui; Rani H Singh
Journal:  Nutrients       Date:  2022-09-29       Impact factor: 6.706

  2 in total

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