Literature DB >> 22718276

Commentary: What degree of hyperphenylalaninaemia requires treatment?

R J Pollitt1.   

Abstract

Despite some 50 years' experience in the treatment of phenylketonuria and numerous scientific publications on the subject there is no clear consensus as to what degree of hyperphenylalaninaemia will result in intellectual impairment. Studies of three main types, on untreated cases of moderate hyperphenylalaninaemia, on treated cases of phenylketonuria, and on the effects of current blood phenylalanine concentration on executive function, have lead to different conclusions. Overall, there appears to be a fairly strong case for limiting dietary treatment to individuals whose blood phenylalanine levels would otherwise exceed 600 μmol/L. This is now policy in some European countries but a formal large-scale study of long-term outcomes to validate the approach is urgently required.

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Year:  2012        PMID: 22718276     DOI: 10.1007/s10545-012-9505-y

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


  19 in total

1.  Effect on intelligence of relaxing the low phenylalanine diet in phenylketonuria.

Authors:  I Smith; M G Beasley; A E Ades
Journal:  Arch Dis Child       Date:  1991-03       Impact factor: 3.791

2.  Cognitive functions in classic phenylketonuria and mild hyperphenylalaninaemia: experience in a paediatric population.

Authors:  Rosa Gassió; Rafael Artuch; Maria Antonia Vilaseca; Eugenia Fusté; Cristina Boix; Anna Sans; Jaume Campistol
Journal:  Dev Med Child Neurol       Date:  2005-07       Impact factor: 5.449

3.  Normal clinical outcome in untreated subjects with mild hyperphenylalaninemia.

Authors:  J Weglage; M Pietsch; R Feldmann; H G Koch; J Zschocke; G Hoffmann; A Muntau-Heger; J Denecke; P Guldberg; F Güttler; H Möller; U Wendel; K Ullrich; E Harms
Journal:  Pediatr Res       Date:  2001-04       Impact factor: 3.756

4.  Prefrontal cortex cognitive deficits in children treated early and continuously for PKU.

Authors:  A Diamond; M B Prevor; G Callender; D P Druin
Journal:  Monogr Soc Res Child Dev       Date:  1997

5.  Intelligence and quality of dietary treatment in phenylketonuria.

Authors:  I Smith; M G Beasley; A E Ades
Journal:  Arch Dis Child       Date:  1990-05       Impact factor: 3.791

6.  Intelligence in mild atypical phenylketonuria.

Authors:  P M Costello; M G Beasley; S L Tillotson; I Smith
Journal:  Eur J Pediatr       Date:  1994-04       Impact factor: 3.183

7.  Stability of blood phenylalanine levels and IQ in children with phenylketonuria.

Authors:  Vera Anastasoaie; Laura Kurzius; Peter Forbes; Susan Waisbren
Journal:  Mol Genet Metab       Date:  2008-08-13       Impact factor: 4.797

Review 8.  Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story. Medical Research Council Working Party on Phenylketonuria.

Authors: 
Journal:  BMJ       Date:  1993-01-09

9.  Phenylalanine blood levels and clinical outcomes in phenylketonuria: a systematic literature review and meta-analysis.

Authors:  Susan E Waisbren; Kay Noel; Kyle Fahrbach; Catherine Cella; Diana Frame; Alex Dorenbaum; Harvey Levy
Journal:  Mol Genet Metab       Date:  2007-06-25       Impact factor: 4.797

10.  High phenylalanine levels directly affect mood and sustained attention in adults with phenylketonuria: a randomised, double-blind, placebo-controlled, crossover trial.

Authors:  Amber E ten Hoedt; Leo M J de Sonneville; Baudouin Francois; Nienke M ter Horst; Mirian C H Janssen; M Estela Rubio-Gozalbo; Frits A Wijburg; Carla E M Hollak; Annet M Bosch
Journal:  J Inherit Metab Dis       Date:  2010-12-10       Impact factor: 4.982

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  1 in total

Review 1.  Different Viewpoints: International Perspectives on Newborn Screening.

Authors:  Rodney J Pollitt
Journal:  J Med Biochem       Date:  2014-10-08       Impact factor: 3.402

  1 in total

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