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Trace element excess in PKU diets?

Authors :
Jürgen Schaub
K. Dörner
Erika Sievers
H. D. Oldigs
Source :
Journal of inherited metabolic disease. 13(6)
Publication Year :
1990

Abstract

Knowledge of trace element requirements of infants with phenylketonuria (PKU) fed a semisynthetic diet is limited. Three infants with PKU detected early were studied longitudinally in classical balance studies for 72 h, under domestic conditions, at the ages of 2, 5, 8, 12 and 16 weeks. Iron, copper and manganese concentrations in the diet and faeces were determined by atomic absorption spectroscopy. The median concentrations in the diet (4.8 mg Fe/L, 1.7 mg Cu/L, 0.43 mg Mn/L) exceed those in human milk. This is mainly due to supplementation of the amino acid preparation used. The increased intake led to a significantly higher daily retention of Cu and Mn from the PKU-diet fed, with a median of 0.17 mg Cu/kg and 6.4 micrograms Mn/kg body weight; the median retention of Fe was 0.24 mg Fe/kg. Our results confirmed the doubts about the suitability of the present trace element supplementation in formula for infants with PKU during the first four months of life.

Details

ISSN :
01418955
Volume :
13
Issue :
6
Database :
OpenAIRE
Journal :
Journal of inherited metabolic disease
Accession number :
edsair.doi.dedup.....8ab5082ff5104174b8a66e28e7e3406f