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Diurnal variation of phenylalanine concentrations in tyrosinaemia type 1: should we be concerned?
Author(s) -
Daly A.,
GokmenOzel H.,
MacDonald A.,
Preece M. A.,
Davies P.,
Chakrapani A.,
McKiernan P.
Publication year - 2012
Publication title -
journal of human nutrition and dietetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.951
H-Index - 70
eISSN - 1365-277X
pISSN - 0952-3871
DOI - 10.1111/j.1365-277x.2011.01215.x
Subject(s) - phenylalanine , medicine , tyrosine , morning , endocrinology , tyrosinemia , plasma concentration , amino acid , biochemistry , chemistry
How to cite this article
Daly A., Gokmen‐Ozel H., MacDonald A., Preece M.A., Davies P., Chakrapani A. & McKiernan P. (2012) Diurnal variation of phenylalanine concentrations in tyrosinaemia type 1: should we be concerned? J Hum Nutr Diet. 25 , 111–116 Abstract Background: Tyrosinaemia type 1 (HT1) is treated with a tyrosine and phenylalanine‐restricted diet, amino acids free of phenylalanine and tyrosine, and nitisinone (NTBC). Treatment guidelines recommend plasma tyrosine between 200–400 μ m and phenylalanine at least >30 μ m . There is little information on the diurnal variation of plasma tyrosine or phenylalanine in HT1. Low plasma phenylalanine <30 μ m may be associated with poor growth and cognitive delay. The present study aimed to document diurnal variation of tyrosine and phenylalanine plasma concentrations and growth in children with HT1. Methods: Median tyrosine and phenylalanine plasma concentrations were reviewed retrospectively over 3 years in 11 subjects (median age 4 years) with HT1. Subjects routinely collected morning fasting blood samples but afternoon nonfasted samples were taken in the clinic (<10% of samples). Growth Z ‐scores were calculated. Results: The percentage of all plasma phenylalanine concentrations <30 μ m was 8.6% and <40 μ m was 13.6%. Only 2% of fasting morning phenylalanine concentrations were <30 μ m , compared to 83% of nonfasting afternoon samples. All but one child had a height Z ‐score <0. Conclusions: Blood phenylalanine concentrations were consistently lower in the afternoon. Taking blood samples at variable time points in the day may lead to variation in interpreting dietary control. A detailed study is necessary to examine the 24‐h diurnal variation of plasma phenylalanine and tyrosine in HT1. It is possible that phenylalanine concentrations may be very low for a substantive time over 24 h and the potential impact that this may have on cognitive development and growth in children is unknown.