Literature DB >> 16988900

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

R Matalon1, K Michals-Matalon, G Bhatia, E Grechanina, P Novikov, J D McDonald, J Grady, S K Tyring, F Guttler.   

Abstract

Large neutral amino acids (LNAAs) have been used on a limited number of patients with phenylketonuria (PKU) with the purpose of decreasing the influx of phenylalanine (Phe) to the brain. In earlier studies on mice with PKU (ENU(2)/ENU(2)), LNAAs were given and a surprising decline in blood Phe concentrations was observed. The formula used in the mouse experiment (PreKUnil) lacked lysine. Therefore, a new formulation of LNAAs (NeoPhe) was developed, introducing changes in the concentration of some amino acids and adding lysine, so that such a mixture could be used in humans. The new formula was found to be effective in reducing blood Phe concentration in mice by about 50% of the elevated levels. Patients with PKU were given LNAAs and blood Phe concentrations were determined in an open-label study. Three centers--in Russia, the Ukraine and the USA--took part in the study. NeoPhe was given at 0.5 g/kg per day in three divided doses to eight subjects with PKU and at 1.0 g/kg per day to three patients, for one week. The NeoPhe resulted in decrease of elevated blood Phe by 50% in both groups. The preliminary data from this study are encouraging and a double blind placebo-controlled trial will be required to show long-term efficacy and tolerance of LNAAs in the treatment of PKU.

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Year:  2006        PMID: 16988900     DOI: 10.1007/s10545-006-0395-8

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


  49 in total

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2.  Influence of phenylalanine intake on phenylketonuria.

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4.  Characterization of mutations at the mouse phenylalanine hydroxylase locus.

Authors:  J D McDonald; C K Charlton
Journal:  Genomics       Date:  1997-02-01       Impact factor: 5.736

5.  Tetrahydrobiopterin responsiveness in a large series of phenylketonuria patients.

Authors:  J Weglage; M Grenzebach; A von Teeffelen-Heithoff; T Marquardt; R Feldmann; J Denecke; D Gödde; H G Koch
Journal:  J Inherit Metab Dis       Date:  2002-08       Impact factor: 4.982

6.  Biopterin responsive phenylalanine hydroxylase deficiency.

Authors:  Reuben Matalon; Richard Koch; Kimberlee Michals-Matalon; Kathryn Moseley; Sankar Surendran; Stephen Tyring; Heidi Erlandsen; Alejandra Gamez; Raymond C Stevens; Anne Romstad; Lisbeth B Møller; Flemming Guttler
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7.  Blood phenylalanine levels and intelligence of 10-year-old children with PKU in the National Collaborative Study.

Authors:  K Michals; C Azen; P Acosta; R Koch; R Matalon
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8.  Neurological outcome in adult patients with early-treated phenylketonuria.

Authors:  J Pietz; R Dunckelmann; A Rupp; D Rating; H M Meinck; H Schmidt; H J Bremer
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9.  Effect of age at loss of dietary control on intellectual performance and behavior of children with phenylketonuria.

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10.  Neurological deterioration in young adults with phenylketonuria.

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Review 3.  Inherited Metabolic Disorders: Aspects of Chronic Nutrition Management.

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4.  Pharmacologic inhibition of L-tyrosine degradation ameliorates cerebral dopamine deficiency in murine phenylketonuria (PKU).

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Review 5.  Nutritional management of PKU with glycomacropeptide from cheese whey.

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Review 6.  What we know that could influence future treatment of phenylketonuria.

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7.  L-carnitine blood levels and oxidative stress in treated phenylketonuric patients.

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8.  Phenylketonuria: an inborn error of phenylalanine metabolism.

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Review 9.  Large neutral amino acids in the treatment of PKU: from theory to practice.

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10.  Interpretation of plasma amino acids in the follow-up of patients: the impact of compartmentation.

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