Literature DB >> 19609714

Metabolic phenotypes of phenylketonuria. Kinetic and molecular evaluation of the Blaskovics protein loading test.

U Langenbeck1, P Burgard, U Wendel, M Lindner, J Zschocke.   

Abstract

BACKGROUND: As part of the German Collaborative Study of Children Treated for Phenylketonuria (PKU), a three-day protein loading test was applied to children at 6 months of age. This load elicits three principal types of blood phenylalanine (Phe) response, with types I and III clinically corresponding to classic PKU and mild hyperphenylalaninaemia not requiring diet (MHP), respectively. An intermediate type II, clinically corresponding to mild PKU, is characterized by early decline of blood Phe from above 1200 micromol/L down to levels between 600 and 1200 micromol/L at 72 h. AIMS: Unbiased classification and kinetic and molecular characterization of the intermediate Phe response; estimation of phenotypic variability of Phe disposal.
METHOD: A kinetic model with zero-order protein synthesis and first-order rate of metabolic disposal of Phe is applied to 157 tests.
RESULTS: A model of exponentially saturated activation describes the acceleration of Phe disposal from day 1 to 3 in the intermediate type of response. Eleven of 14 p.Y414C functional hemizygotes and two of three p.R261Q homozygotes manifested this kinetic type. The rate estimates of Phe metabolic disposal differ widely in patients with identical PAH genotype, yet are highly correlated with the Phe level at 72 h.

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Year:  2009        PMID: 19609714     DOI: 10.1007/s10545-009-1152-6

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


  28 in total

1.  In vivo enzyme activity in inborn errors of metabolism.

Authors:  G N Thompson; J H Walter; J V Leonard; D Halliday
Journal:  Metabolism       Date:  1990-08       Impact factor: 8.694

2.  Phenylketonuria mutations in Germany.

Authors:  J Zschocke; G F Hoffmann
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Review 3.  Monogenic traits are not simple: lessons from phenylketonuria.

Authors:  C R Scriver; P J Waters
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Authors:  M E Blaskovics; G E Schaeffler; S Hack
Journal:  Arch Dis Child       Date:  1974-11       Impact factor: 3.791

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Authors:  J L Berman; G C Cunningham; R W Day; R Ford; D Y Hsia
Journal:  Am J Dis Child       Date:  1969-01

6.  The activity of wild-type and mutant phenylalanine hydroxylase and its regulation by phenylalanine and tetrahydrobiopterin at physiological and pathological concentrations: an isothermal titration calorimetry study.

Authors:  Angel L Pey; Aurora Martinez
Journal:  Mol Genet Metab       Date:  2005-06-03       Impact factor: 4.797

7.  Molecular basis of phenotypic heterogeneity in phenylketonuria.

Authors:  Y Okano; R C Eisensmith; F Güttler; U Lichter-Konecki; D S Konecki; F K Trefz; M Dasovich; T Wang; K Henriksen; H Lou
Journal:  N Engl J Med       Date:  1991-05-02       Impact factor: 91.245

8.  Phenylalanine hydroxylase genotypes, predicted residual enzyme activity and phenotypic parameters of diagnosis and treatment of phenylketonuria.

Authors:  P Burgard; A Rupp; D S Konecki; F K Trefz; H Schmidt; U Lichter-Konecki
Journal:  Eur J Pediatr       Date:  1996-07       Impact factor: 3.183

9.  L-phenylalanine binding and domain organization in human phenylalanine hydroxylase: a differential scanning calorimetry study.

Authors:  Matthías Thórólfsson; Beatriz Ibarra-Molero; Peter Fojan; Steffen B Petersen; Jose M Sanchez-Ruiz; Aurora Martínez
Journal:  Biochemistry       Date:  2002-06-18       Impact factor: 3.162

10.  Molecular genetics of tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency.

Authors:  Marcel R Zurflüh; Johannes Zschocke; Martin Lindner; François Feillet; Céline Chery; Alberto Burlina; Raymond C Stevens; Beat Thöny; Nenad Blau
Journal:  Hum Mutat       Date:  2008-01       Impact factor: 4.878

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  3 in total

1.  Development of Metabolic Phenotype in Phenylketonuria: Evaluation of the Blaskovics Protein Loading Test at 5 Years of Age.

Authors:  P Burgard; E Mönch; J Zschocke; U Wendel; U Langenbeck
Journal:  JIMD Rep       Date:  2015-12-19

2.  Utility of phenylalanine hydroxylase genotype for tetrahydrobiopterin responsiveness classification in patients with phenylketonuria.

Authors:  Meghan E Quirk; Steven F Dobrowolski; Benjamin E Nelson; Bradford Coffee; Rani H Singh
Journal:  Mol Genet Metab       Date:  2012-07-20       Impact factor: 4.797

3.  Cardiac teratogenicity in mouse maternal phenylketonuria: defining phenotype parameters and genetic background influences.

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Journal:  Mol Genet Metab       Date:  2012-08-08       Impact factor: 4.797

  3 in total

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