Literature DB >> 9266384

Treatment products and approaches for phenylketonuria: improved palatability and flexibility demonstrate safety, efficacy and acceptance in US clinical trials.

A P Prince1, M P McMurray, N R Buist.   

Abstract

A new amino acid formulation and a variety of treatment products incorporating it were evaluated for long-term safety, efficacy, and acceptance in 25 subjects with phenylketonuria over a period of 5 years. Palatability of the treatment was improved by reducing the required intake of amino acids, reformulating the mixture to have better taste, and providing vitamins and minerals as tablets. The hypotheses were that these strategies would improve compliance and metabolic control and maintain nutritional status in subjects. Compliance with treatment was determined from mean reported intakes (4-day diet records) and from mean 'received' intakes using receipts of treatment products actually shipped to individuals upon request. Mean amino acid intakes prescribed were significantly reduced from study entry to end, from 1.2 g/kg to 0.7 g/kg (p < 0.001). Reported intakes were similarly reduced from 1.3 g/kg to 0.7 g/kg (p < 0.001). While actually 'received' intakes of amino acid formula were also significantly reduced (p < 0.001), intakes by this measure were much lower than either prescribed or reported, 0.9 g/kg at entry and 0.4 g/kg at the end of the study, suggesting that acceptance of the treatment (usage of products), even when made more palatable, is below clinical expectations. In spite of these findings, mean serum proteins and minerals, height and weight were not significantly reduced during the study, supporting the safety of lowered intakes of amino acids and of nutritionally incomplete products. While the increase in mean serum phenylalanine concentration from 0.38 to 0.48 mmol/L was significant (p < 0.03), this mean rise of 0.1 mmol/L during a corresponding mean age increase of 4.2 years (from 6.9 to 11.1 years) is lower than in other recent reports from longitudinal studies of outcomes during this age range in subjects treated with traditional products. These data support the safety and efficacy of a more palatable and flexible approach to treatment.

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Year:  1997        PMID: 9266384     DOI: 10.1023/a:1005337126669

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  15 in total

1.  A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS.

Authors:  R GUTHRIE; A SUSI
Journal:  Pediatrics       Date:  1963-09       Impact factor: 7.124

2.  Routine measurement of calcium, magnesium, copper, zinc, and iron in urine and serum by inductively coupled plasma emission spectroscopy.

Authors:  D E Nixon; T P Moyer; P Johnson; J T McCall; A B Ness; W H Fjerstad; M B Wehde
Journal:  Clin Chem       Date:  1986-09       Impact factor: 8.327

3.  Laser immunonephelometry reference intervals for eight serum proteins in healthy children.

Authors:  D J Malvy; J D Povéda; M Debruyne; B Montagnon; B Burtschy; C Herbert; P Cacès; O Houot; O Amédée-Manesme
Journal:  Clin Chem       Date:  1992-03       Impact factor: 8.327

4.  Zinc and copper status of treated children with phenylketonuria.

Authors:  P B Acosta; P M Fernhoff; H S Warshaw; K M Hambidge; A Ernest; E R McCabe; L J Elsas
Journal:  JPEN J Parenter Enteral Nutr       Date:  1981 Sep-Oct       Impact factor: 4.016

5.  Recommendations on the dietary management of phenylketonuria. Report of Medical Research Council Working Party on Phenylketonuria.

Authors: 
Journal:  Arch Dis Child       Date:  1993-03       Impact factor: 3.791

6.  Physical growth of children treated for phenylketonuria.

Authors:  M A McBurnie; R A Kronmal; V E Schuett; R Koch; C G Azeng
Journal:  Ann Hum Biol       Date:  1991 Jul-Aug       Impact factor: 1.533

7.  Intellectual development in 12-year-old children treated for phenylketonuria.

Authors:  C G Azen; R Koch; E G Friedman; S Berlow; J Coldwell; W Krause; R Matalon; E McCabe; M O'Flynn; R Peterson
Journal:  Am J Dis Child       Date:  1991-01

8.  An occipito-temporal syndrome in adolescents with optimally controlled hyperphenylalaninaemia.

Authors:  H C Lou; P B Toft; J Andresen; I Mikkelsen; B Olsen; F Güttler; S Wieslander; O Henriksen
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

9.  Serum selenium levels in individuals on PKU diets.

Authors:  G Darling; P Mathias; M O'Regan; E Naughten
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

10.  Long-term development of intelligence (IQ) and EEG in 34 children with phenylketonuria treated early.

Authors:  J Pietz; C Benninger; H Schmidt; D Scheffner; H Bickel
Journal:  Eur J Pediatr       Date:  1988-05       Impact factor: 3.183

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  12 in total

Review 1.  Phenylketonuria: old disease, new approach to treatment.

Authors:  H L Levy
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

2.  Living with phenylketonuria: perspectives of patients and their families.

Authors:  C Bilginsoy; N Waitzman; C O Leonard; S L Ernst
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

3.  Behavioural factors related to metabolic control in patients with phenylketonuria.

Authors:  M R Crone; F J van Spronsen; K Oudshoorn; J Bekhof; G van Rijn; P H Verkerk
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

4.  Nutritional Management of Phenylketonuria.

Authors:  Erin L Macleod; Denise M Ney
Journal:  Ann Nestle Eng       Date:  2010-06

5.  Tetrahydrobiopterin (BH4) in PKU: effect on dietary treatment, metabolic control, and quality of life.

Authors:  B Ziesch; J Weigel; A Thiele; U Mütze; C Rohde; U Ceglarek; J Thiery; W Kiess; S Beblo
Journal:  J Inherit Metab Dis       Date:  2012-03-06       Impact factor: 4.982

6.  Acceptability of a new modular protein substitute for the dietary treatment of phenylketonuria.

Authors:  F J Rohr; A W Munier; H L Levy
Journal:  J Inherit Metab Dis       Date:  2001-11       Impact factor: 4.982

Review 7.  Protein substitutes for PKU: what's new?

Authors:  A Macdonald; A Daly; P Davies; D Asplin; S K Hall; G Rylance; A Chakrapani
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

8.  Protein substitute dosage in PKU: how much do young patients need?

Authors:  A MacDonald; A Chakrapani; C Hendriksz; A Daly; P Davies; D Asplin; K Hall; I W Booth
Journal:  Arch Dis Child       Date:  2006-03-17       Impact factor: 3.791

9.  Are tablets a practical source of protein substitute in phenylketonuria?

Authors:  A MacDonald; C Ferguson; G Rylance; A A M Morris; D Asplin; S K Hall; I W Booth
Journal:  Arch Dis Child       Date:  2003-04       Impact factor: 3.791

Review 10.  The complete European guidelines on phenylketonuria: diagnosis and treatment.

Authors:  A M J van Wegberg; A MacDonald; K Ahring; A Bélanger-Quintana; N Blau; A M Bosch; A Burlina; J Campistol; F Feillet; M Giżewska; S C Huijbregts; S Kearney; V Leuzzi; F Maillot; A C Muntau; M van Rijn; F Trefz; J H Walter; F J van Spronsen
Journal:  Orphanet J Rare Dis       Date:  2017-10-12       Impact factor: 4.123

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