Fj. Vanspronsen et al., PHENYLKETONURIA - THE IN-VIVO HYDROXYLATION RATE OF PHENYLALANINE INTO TYROSINE IS DECREASED, The Journal of clinical investigation, 101(12), 1998, pp. 2875-2880
In phenylketonuria (PKU), the enzyme phenylalanine hydroxylase is defi
cient, resulting in a decreased conversion of phenylalanine (Phe) into
tyrosine (Tyr). The severity of the disease is expressed as the toler
ance for Phe at 5 yr of age. In PKU patients it is assumed that the de
creased conversion of Phe into Tyr is directly correlated with the tol
erance for Phe. We investigated this correlation by an in vivo stable
isotope study. The in vivo residual hydroxylation was quantitated usin
g a primed continuous infusion of L-[ring-H-2(5)]Phe and L-[1-C-13]Tyr
and the determination of the isotopic enrichments of L-[ring-H-2(5)]P
he, L-[ring-H-2(4)]Tyr, and L-[1-C-13]Tyr in plasma. Previous reports
by Thompson and coworkers (Thompson, G.N., and D. Halliday. 1990. J. C
lin. Invest. 86:317-322; Thompson, G.N., J.H. Waiter, J.V. Leonard, an
d D. Halliday. 1990, Metabolism. 39:799-807; Treacy, E., J.J. Pitt, K.
Seller, G.N. Thompson, S. Ramus, and R.G.H. Cotton. 1996. J. Inherite
d Metab. Dis. 19:595-602), applying the same technique, showed normal
in vivo hydroxylation rates of Phe in almost all PKU patients. Therefo
re, our study was divided up in two parts, First, the method was re-ev
aluated. Second, the correlation between the in vivo hydroxylation of
Phe and the tolerance for Phe was tested in seven classical PKU patien
ts. Very low (0.13-0.95 mu mol/kg per hour) and normal (4.11 and 6.33
mu mol/kg per hour) conversion rates were found in patients and contro
ls, respectively. Performing the infusion study twice in the same pati
ent and wash-out studies of the labels at the end of the experiment in
a patient and control showed that the method is applicable in PKU pat
ients and gives consistent data. No significant correlation was observ
ed between the in vivo hydroxylation rates and the tolerances. The res
ults of this study, therefore, showed that within the group of patient
s with classical PKU, the tolerance does not depend on the in vivo hyd
roxylation.