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Utilisation of amino acid mixtures in adolescents with phenylketonuria

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Abstract

The nutritional regimen of patients with phenylketonuria (PKU) comprises a diet of natural proteins and phenylalanine(Phe)-free amino acid (AA) mixture. The main daily protein requirement is covered by a Phe-free A A mixture. In an adult with PKU, the consumption of the daily AA requirement in one single dose at breakfast caused nausea and vomiting. Therefore, four studies were designed to investigate the adverse and metabolic effects resulting from large intakes of AA mixtures used in the treatment of PKU patients with respect to the following: (1) biochemical effects following consumption of one single dose of Phe-free AA mixture in healthy persons; (2) transient metabolic changes caused by different individual regimens of AA intake in healthy persons and in one PKU patient; (3) nitrogen excretion in PKU patients taking the AA mixture in two or three portions; and (4) catabolic metabolism of AA in a PKU patient. In healthy subjects following the ingestion of the AA mixture in one bolus there was an increase in the blood levels of the given AA and also an increase in blood insulin concentration and a decrease in blood glucose concentration. These changes were less marked when the AA mixture was divided into three portions per day. In contrast, in a PKU patient following the ingestion of AA there was an increase in blood glucose. The urinary nitrogen excretion was greater in PKU patients when one compared to three portions of AA mixture was taken. The consumption of the daily requirement of AA mixture in one single does produced increased catabolism in a PKU patient In conclusion it is recommended that the total daily amount of AA mixture should be divided into a minimum o three portions.

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Abbreviations

AA :

amino acid

Phe :

phenylalanine

PKU :

phenylketonuria

References

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Mönch, E., Herrmann, M.E., Brösicke, H. et al. Utilisation of amino acid mixtures in adolescents with phenylketonuria. Eur J Pediatr 155 (Suppl 1), S115–S120 (1996). https://doi.org/10.1007/PL00014226

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  • DOI: https://doi.org/10.1007/PL00014226

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