Literature DB >> 10685924

Effect of genotype on changes in intelligence quotient after dietary relaxation in phenylketonuria and hyperphenylalaninaemia.

L G Greeves1, C C Patterson, D J Carson, R Thom, M C Wolfenden, J Zschocke, C A Graham, N C Nevin, E R Trimble.   

Abstract

BACKGROUND: Associations between genotype and intellectual outcome in patients with phenylketonuria are complicated because intelligence is influenced by many variables, including environmental factors and other genetic determinants. Intellectual changes with age, both on and after relaxation of diet, vary within the patient population. This study aims to determine whether a significant association exists between genotype and change in intelligence after relaxation of diet.
METHODS: 125 patients with hyperphenylalaninaemia and phenylketonuria whose diet was relaxed after 8 years of age. Verbal, performance, and full scale intelligence quotients at 8, 14, and 18 years were expressed as standard deviation scores (IQ-SDS), and genotype as predicted residual enzyme activity (PRA) of phenylalanine hydroxylase.
RESULTS: IQ-SDS at 8, 14, and 18 years were significantly below normal; no association was found between PRA and IQ-SDS. Significant reductions in verbal and full scale IQ-SDS occurred between 8 and 14 years and 8 and 18 years. There was a significant association between PRA and the reduction in verbal, performance, and full scale IQ between these years. Multiple regression analysis of 18 year results, using 8 year results as covariates, supported the association between PRA and IQ-SDS; after adjustment for phenylalanine control, both up to and after the age of 8 years, the full scale IQ-SDS at 14 and 18 years was 0.15 higher for each 10% increase in PRA.
CONCLUSIONS: Genotype might be useful in predicting the likelihood of intellectual change in patients with hyperphenylalaninaemia and phenylketonuria whose diet is relaxed after the age of 8 years.

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Year:  2000        PMID: 10685924      PMCID: PMC1718236          DOI: 10.1136/adc.82.3.216

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  41 in total

Review 1.  PKU in adolescents: rationale and psychosocial factors in diet continuation.

Authors:  H L Levy; S E Waisbren
Journal:  Acta Paediatr Suppl       Date:  1994-12

Review 2.  Diet termination in children with phenylketonuria: a review of psychological assessments used to determine outcome.

Authors:  S E Waisbren; R R Schnell; H L Levy
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

3.  Diet discontinuation policies and practices of PKU clinics in the United States.

Authors:  V E Schuett; R F Gurda; E S Brown
Journal:  Am J Public Health       Date:  1980-05       Impact factor: 9.308

4.  Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria.

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Journal:  Br Med J       Date:  1978-09-09

Review 5.  Mutations in the phenylalanine hydroxylase gene: genetic determinants for the phenotypic variability of hyperphenylalaninemia.

Authors:  F Güttler; P Guldberg
Journal:  Acta Paediatr Suppl       Date:  1994-12

6.  Automated sequencing detects all mutations in Northern Irish patients with phenylketonuria and mild hyperphenylalaninaemia.

Authors:  J Zschocke; C A Graham; F J Stewart; D J Carson; N C Nevin
Journal:  Acta Paediatr Suppl       Date:  1994-12

7.  Discordant phenylketonuria phenotypes in one family: the relationship between genotype and clinical outcome is a function of multiple effects.

Authors:  L A Tyfield; J Zschocke; A Stephenson; F Cockburn; A Harvie; J L Bidwell; N A Wood; L P Hunt
Journal:  J Med Genet       Date:  1995-11       Impact factor: 6.318

8.  Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approach.

Authors:  J Zschocke; C A Graham; D J Carson; N C Nevin
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

Review 9.  Long-term follow-up of children with classical phenylketonuria after diet discontinuation: a review.

Authors:  U Potocnik; K Widhalm
Journal:  J Am Coll Nutr       Date:  1994-06       Impact factor: 3.169

10.  A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype.

Authors:  P Guldberg; F Rey; J Zschocke; V Romano; B François; L Michiels; K Ullrich; G F Hoffmann; P Burgard; H Schmidt; C Meli; E Riva; I Dianzani; A Ponzone; J Rey; F Güttler
Journal:  Am J Hum Genet       Date:  1998-07       Impact factor: 11.025

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