Literature DB >> 3171015

Blood phenylalanine levels and intelligence of 10-year-old children with PKU in the National Collaborative Study.

K Michals1, C Azen, P Acosta, R Koch, R Matalon.   

Abstract

Dietary intakes and blood phenylalanine levels of 125 10-year-old children with PKU are reported. Of those patients, 59 discontinued the special diet at 6 years, 16 discontinued at 8 years, 5 discontinued at 6 years but returned to the diet at 8 1/2 years, and 45 continued the diet to 10 years. Phenylalanine intake was determined by 2-day diet records. Blood phenylalanine concentrations revealed a lack of clear distinction between the diet groups; therefore, regression analysis was performed on the group as a whole. The analyses revealed significant relationships between blood phenylalanine levels from ages 6 to 10 years and each of the cognitive outcome variables, after the influences of parental IQ and the age at which treatment was initiated were controlled for. Intelligence test scores were also related to phenylalanine levels between ages 3 1/2 and 5 1/2 years. The findings suggest that dietary restriction of phenylalanine should continue in patients with PKU through at least 10 years of age.

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Year:  1988        PMID: 3171015

Source DB:  PubMed          Journal:  J Am Diet Assoc        ISSN: 0002-8223


  14 in total

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Authors:  H Dotremont; B François; M Diels; P Gillis
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

2.  Large neutral amino acids in the treatment of phenylketonuria (PKU).

Authors:  R Matalon; K Michals-Matalon; G Bhatia; E Grechanina; P Novikov; J D McDonald; J Grady; S K Tyring; F Guttler
Journal:  J Inherit Metab Dis       Date:  2006-09-21       Impact factor: 4.982

3.  Phenylketonuric patients decades after diet.

Authors:  R O Fisch; P N Chang; S Weisberg; P Guldberg; F Güttler; M Y Tsai
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

4.  Low iron stores in infants and children with treated phenylketonuria: a population at risk for iron-deficiency anaemia and associated cognitive deficits.

Authors:  J L Bodley; V J Austin; W B Hanley; J T Clarke; S Zlotkin
Journal:  Eur J Pediatr       Date:  1993-02       Impact factor: 3.183

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6.  Insurance coverage of special foods needed in the treatment of phenylketonuria.

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Journal:  Public Health Rep       Date:  1993 Jan-Feb       Impact factor: 2.792

7.  Pregnancy in phenylketonuria: dietary treatment aimed at normalising maternal plasma phenylalanine concentration.

Authors:  G N Thompson; D E Francis; D M Kirby; R Compton
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8.  Dietary interventions for phenylketonuria.

Authors:  Elisabeth Jameson; Tracey Remmington
Journal:  Cochrane Database Syst Rev       Date:  2020-07-16

Review 9.  Phenylketonuria: a review of current and future treatments.

Authors:  Naz Al Hafid; John Christodoulou
Journal:  Transl Pediatr       Date:  2015-10

10.  The response of patients with phenylketonuria and elevated serum phenylalanine to treatment with oral sapropterin dihydrochloride (6R-tetrahydrobiopterin): a phase II, multicentre, open-label, screening study.

Authors:  B K Burton; D K Grange; A Milanowski; G Vockley; F Feillet; E A Crombez; V Abadie; C O Harding; S Cederbaum; D Dobbelaere; A Smith; A Dorenbaum
Journal:  J Inherit Metab Dis       Date:  2007-09-12       Impact factor: 4.982

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