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Longitudinal Dietary Intake Data in Patients with Phenylketonuria from Europe: The Impact of Age and Phenylketonuria Severity

  • Alex Pinto
  • , Kirsten Ahring
  • , Manuela Ferreira Almeida
  • , Catherine Ashmore
  • , Amaya Bélanger-Quintana
  • , Alberto Burlina
  • , Turgay Coşkun
  • , Anne Daly
  • , Esther van Dam
  • , Ali Dursun
  • , Sharon Evans
  • , François Feillet
  • , Maria Giżewska
  • , Hulya Gökmen-Özel
  • , Mary Hickson
  • , Yteke Hoekstra
  • , Fatma Ilgaz
  • , Richard Jackson
  • , Alicja Leśniak
  • , Christian Loro
  • Katarzyna Malicka, Michał Patalan, Júlio César Rocha, Serap Sivri, Iris Rodenburg, Francjan van Spronsen, Kamilla Strączek, Ayşegül Tokatli, Anita MacDonald
  • Birmingham Women's and Children's NHS Foundation Trust
  • University of Plymouth
  • University of Copenhagen
  • Centro de Genética Médica
  • Centro de Referência na área de Doenças Hereditárias do Metabolismo
  • University of Porto
  • Hospital Ramon y Cajal
  • Azienda Ospedaliera di Padova
  • University of Groningen
  • CHU de Nancy
  • Pomeranian Medical University in Szczecin
  • University of Liverpool
  • NOVA University Lisbon
  • Reference Centre of Inherited Metabolic Diseases
  • Hacettepe University

Araştırma çıktısı: Dergiye katkıMakaleHakem

3 Alıntılar (Scopus)

Özet

In phenylketonuria (PKU), natural protein intake is thought to increase with age, particularly during childhood and adolescence. Longitudinal dietary intake data are scarce and lifelong phenylalanine tolerance remains unknown. Nine centres managing PKU in Europe and Turkey participated in a retrospective study. Data were collected from dietetic records between 2012 and 2018 on phenylalanine (Phe), natural protein, and protein substitute intake. A total of 1323 patients (age range: 1–57 y; 51% male) participated. Dietary intake data were available on 1163 (88%) patients. Patient numbers ranged from 59 to 320 in each centre. A total of 625 (47%) had classical PKU (cPKU), n = 357 (27%) had mild PKU (mPKU), n = 325 (25%) had hyperphenylalaninemia (HPA), and n = 16 (1%) were unknown. The mean percentage of blood Phe levels within target ranged from 65 ± 54% to 88 ± 49%. When intake was expressed as g/day, the mean Phe/natural protein and protein equivalent from protein substitute gradually increased during childhood, reaching a peak in adolescence, and then remained consistent during adulthood. When intake was expressed per kg body weight (g/kg/day), there was a decline in Phe/natural protein, protein equivalent from protein substitute, and total protein with increasing age. Overall, the mean daily intake (kg/day) was as follows: Phe, 904 mg ± 761 (22 ± 23 mg/kg/day), natural protein 19 g ± 16 (0.5 g/kg/day ± 0.5), protein equivalent from protein substitute 39 g ± 22 (1.1 g/kg/day ± 0.6), and total protein 59 g ± 21 (1.7 g/kg/day ± 0.6). Natural protein tolerance was similar between males and females. Patients with mPKU tolerated around 50% less Phe/natural protein than HPA, but 50% more than cPKU. Higher intakes of natural protein were observed in Southern Europe, with a higher prevalence of HPA and mPKU compared with patients from Northern European centres. Natural protein intake doubled with sapropterin usage. In sapropterin-responsive patients, 31% no longer used protein substitutes. Close monitoring and optimisation of protein intake prescriptions are needed, along with future guidelines specifically for different age groups and severities.

Orijinal dilİngilizce
Makale numarası2909
DergiNutrients
Hacim16
Basın numarası17
DOI'lar
Yayın durumuYayınlandı - Eyl 2024

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