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Romanian Academy
The Publishing House of the Romanian Academy
ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
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Acta Endocrinologica (Buc)
Mihali CV, Petrescu CM, Ladasiu-Ciolacu FC, Mândrutiu I, Bechet D, Nistor T, Ardelean A, Benga G
Plasma Phenylalanine Determination By Quantitative Densitometry of Thin Layer Chromatograms and by High Performance Liquid Chromatography in Relation with Modern Management of Phenylketonuria
Acta Endo (Buc) 2018, 14 (4): 556-561doi: 10.4183/aeb.2018.556
Background. The modern management of
phenylketonuria (PKU) consists of generalized newborn
screening (NBS) for hyperphenylalaninemia (HPA),
confirmation of HPA in children detected in the NBS,
introduction of dietary treatment in the first weeks of life,
followed by monitoring the treatment of PKU for decades
to maintain phenylalaninemia within the limits that will
not affect the brain. The present study aimed to evaluate
the usefulness of two chromatographic methodologies for
determination of plasma Phe level in the routine management
of PKU: the two dimensional thin layer chromatography (2D
- TLC) and the high performance liquid chromatography
(HPLC) procedures, respectively.
Material and Methods. Samples of blood from 23
children with HPA detected by neonatal screening or with
confirmed PKU who received treatment by low-Phe diet
were analyzed to estimate the plasma Phe level by the two
chromatographic procedures.
Results. In case of three subjects the very low
concentrations of plasma Phe could not be detected by the
2D - TLC methodology, since the spot was not visible on the
chromatogram. In four patients the differences between the
values of plasma Phe determined by the two methodologies
are not statistically significant, while in fifteen subjects the
differences are highly statistically significant. This is due
to the greater errors that appear in the case of 2D - TLC
methodology. In the range of concentrations of plasma
Phe higher than 360 μmol/L (which is the cut-off value
for HPA), although in four cases there were statistically
significant differences in the level of plasma Phe determined
by the two methodologies, the value obtained by the 2D
- TLC methodology was high enough to influence the
decision of changing the diet so that HPA is kept under
control. In addition, the intense spot of Phe on the 2D - TLC
chromatogram may be detected even by un unexperienced
laboratory specialist.
Conclusion. The HPLC procedure for measurement
of plasma Phe level is very suitable to be used in the routine
management of PKU. The 2D - TLC procedure may be
accompanied by relatively high errors; however, it detects
patients with severe PKU.
Keywords: phenylalanine (Phe), phenylketonuria
(PKU), hyperphenylalaninemia (HPA), high performance
liquid chromatography (HPLC), thin layer chromatography
(TLC).
Correspondence: Gheorghe Benga, MD, PhD, Aleea Muscel No. 19, Ap. 11, 400076, Cluj-Napoca, Romania, E-mail: gbgbenga@
gmail.com