Phenylalanine free infant formula in the dietary management of phenylketonuria

被引:4
|
作者
Yilmaz, Ozlem [1 ,2 ]
Cochrane, Barbara [3 ]
Wildgoose, Jo [4 ]
Pinto, Alex [1 ]
Evans, Sharon [1 ]
Daly, Anne [1 ]
Ashmore, Catherine [1 ]
MacDonald, Anita [1 ]
机构
[1] Birmingham Womens & Childrens Hosp, Birmingham B4 6NH, England
[2] Ankara Yildirim Beyazit Univ, Dept Nutr & Dietet, TR-06760 Ankara, Turkiye
[3] Queen Elizabeth Hosp, Royal Hosp Children, Dietet Dept, Glasgow 51 4TF, Scotland
[4] Bradford Childrens Hosp, Bradford BD5 0NA, England
关键词
Phenylketonuria; Infancy; Infant protein substitute; Formula; Acceptability; Growth; NEUTRAL AMINO-ACIDS; PROTEIN-INTAKE; GROWTH; CHILDREN; OSMOLALITY; SUBSTITUTE; NUTRITION; MIXTURE; WEIGHT; PKU;
D O I
10.1186/s13023-023-02621-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
BackgroundPhenylalanine-free infant formula is an essential source of safe protein in a phenylalanine restricted diet, but its efficacy is rarely studied. We report a multicentre, open, longitudinal, prospective intervention study on a phenylalanine-free infant formula (PKU Start: Vitaflo International Ltd.).ResultsThis was a 2-part study: part I (28 days short term evaluation) and part II (12 months extension). Data was collected on infant blood phenylalanine concentrations, dietary intake, growth, and gastrointestinal tolerance. Ten infants (n = 8 males, 80%), with a median age of 14 weeks (range 4-36 weeks) were recruited from 3 treatment centres in the UK. Nine of ten infants completed the 28-day follow-up (one caregiver preferred the usual phenylalanine-free formula and discontinued the study formula after day 14) and 7/9 participated in study part II. The phenylalanine-free infant formula contributed a median of 57% (IQR 50-62%) energy and 53% (IQR 33-66%) of total protein intake from baseline to the end of the part II extension study. During the 12-month follow-up, infants maintained normal growth and satisfactory blood phenylalanine control. Any early gastrointestinal symptoms (constipation, colic, vomiting and poor feeding) improved with time.ConclusionThe study formula was well tolerated, helped maintain good metabolic control, and normal growth in infants with PKU. The long-term efficacy of phenylalanine-free infant formula should continue to be observed and monitored.
引用
收藏
页数:13
相关论文
共 50 条
  • [1] Phenylalanine free infant formula in the dietary management of phenylketonuria
    Ozlem Yilmaz
    Barbara Cochrane
    Jo Wildgoose
    Alex Pinto
    Sharon Evans
    Anne Daly
    Catherine Ashmore
    Anita MacDonald
    Orphanet Journal of Rare Diseases, 18
  • [2] Phenylalanine-Free Infant Formula in Patients with Phenylketonuria: A Retrospective Study
    Nas, Ozlem Yilmaz
    Ashmore, Catherine
    Evans, Sharon
    Pinto, Alex
    Daly, Anne
    Yabanci Ayhan, Nurcan
    Macdonald, Anita
    NUTRIENTS, 2024, 16 (14)
  • [3] A phenylalanine-free recombinant nutritional protein for the dietary management of phenylketonuria
    Muecke, Yvonne
    Jablonka, Natalia
    Rimann, Nicole
    Grisch-Chan, Hiu Man
    Hoffmann, Bernhard
    Schillberg, Stefan
    Thony, Beat
    Rasche, Stefan
    JOURNAL OF INHERITED METABOLIC DISEASE, 2024, 47 (04) : 651 - 663
  • [4] Changing dietary practices in phenylketonuria
    MacDonald, Anita
    Gokmen-Ozel, Hulya
    Daly, Anne
    TURKISH JOURNAL OF PEDIATRICS, 2009, 51 (05) : 409 - 415
  • [5] Phenylalanine Tolerance over Time in Phenylketonuria: A Systematic Review and Meta-Analysis
    Pinto, Alex
    Ilgaz, Fatma
    Evans, Sharon
    van Dam, Esther
    Rocha, Julio Cesar
    Karabulut, Erdem
    Hickson, Mary
    Daly, Anne
    MacDonald, Anita
    NUTRIENTS, 2023, 15 (16)
  • [6] A new ready for use phenylalanine-free formula for infants with phenylketonuria - Short communication
    Koletzko, B
    Dokoupil, K
    vonSchenck, U
    MONATSSCHRIFT KINDERHEILKUNDE, 1996, 144 (11) : 1248 - 1251
  • [7] Dietary management practices in phenylketonuria across European centres
    Ahring, Kirsten
    Belanger-Quintana, Amaya
    Dokoupil, Katharina
    Ozel, Hulya Gokmen
    Lammardo, Anna Maria
    MacDonald, Anita
    Motzfeldt, Kristina
    Nowacka, Maria
    Robert, Martine
    van Rijn, Margreet
    CLINICAL NUTRITION, 2009, 28 (03) : 231 - 236
  • [8] Physical development in patients with phenylketonuria on dietary treatment: A retrospective study
    Belanger-Quintana, Amaya
    Martinez-Pardo, Mercedes
    MOLECULAR GENETICS AND METABOLISM, 2011, 104 (04) : 480 - 484
  • [9] ENZYMATIC PHENYLALANINE ESTIMATION FOR THE MANAGEMENT OF PATIENTS WITH PHENYLKETONURIA
    WENDEL, U
    KOPPELKAMM, M
    HUMMEL, W
    CLINICA CHIMICA ACTA, 1991, 201 (1-2) : 95 - 98
  • [10] The Effect of Phenylalanine Restricted Diet on Anthropometric Parameters in Classical Phenylketonuria Patients
    Kose, Engin
    Ozturk, Hatice
    Ozdemir, Baransel
    Ozcelik, Recep Eren
    Ciftci, Lutfiye
    Cetin, Kubra
    Ozturk, Fatih
    Arslan, Nur
    IZMIR DR BEHCET UZ COCUK HASTANESI DERGISI, 2019, 9 (01): : 29 - 33