Development of metabolic phenotype in phenylketonuria: evaluation of the blaskovics protein loading test at 5 Years of age
Background: As part of the German Collaborative Study on Phenylketonuria (PKU)/Hyperphenylalaninaemia (HPA) Study Protocol, a Blaskovics protein loading test (180 mg phenylalanine (phe) protein equivalent per kg body weight and day for 72 h) had been applied to 145 children at the age of 6 months. F...
Gespeichert in:
| Hauptverfasser: | , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2016
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| In: |
JIMD reports
Year: 2015, Jahrgang: 29, Pages: 77-84 |
| ISSN: | 2192-8312 |
| DOI: | 10.1007/8904_2015_508 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1007/8904_2015_508
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| Verfasserangaben: | P. Burgard, E. Mönch, J. Zschocke, U. Wendel, U. Langenbeck |
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| 245 | 1 | 0 | |a Development of metabolic phenotype in phenylketonuria |b evaluation of the blaskovics protein loading test at 5 Years of age |c P. Burgard, E. Mönch, J. Zschocke, U. Wendel, U. Langenbeck |
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| 520 | |a Background: As part of the German Collaborative Study on Phenylketonuria (PKU)/Hyperphenylalaninaemia (HPA) Study Protocol, a Blaskovics protein loading test (180 mg phenylalanine (phe) protein equivalent per kg body weight and day for 72 h) had been applied to 145 children at the age of 6 months. For investigating possible age-related changes of metabolic phenotype, 51 of them received a 2nd loading test at 5 years of age. Methods: Besides the analysis of blood phe levels, acidic phe transamination metabolites were quantified in urine. Results: Compared to the 6-month data, the mean blood phe level 72 h after start of loading (Phe72) was found to be decreased by 7% (P = 0.06), whereas the mean urinary excretion (per 1.73 m2 body surface and day) of 2-hydroxyphenylacetic acid was increased 1.9-fold (P < 0.01). Corresponding with these analytical data, the kinetic model constant k out of metabolic plus renal phe disposal was found increased 1.3-fold in mean (P < 0.01).In 3 of the 51 patients, Phe72 was very high at 6 months while in the medium range at 5 years, suggesting that catabolic states may mimic a more severe metabolic defect.The blood phe level response of mild PKU (type II) was assigned identically at both ages in 7/9 patients. Diverging results were (i) response type III (mild hyperphenylalaninaemia) at 6 months and type II at 5 years and (ii) type II at 6 months and type III at age 5. Conclusion: Renal elimination of OHPAA and phe tolerance increase significantly between the age of 6 months and 5 years, suggesting that, at least in childhood, formation and/or renal disposal of phe transamination metabolites may be major distal determinants of phe tolerance. | ||
| 534 | |c 2015 | ||
| 650 | 4 | |a Kinetic Model Type | |
| 650 | 4 | |a Mild Hyperphenylalaninaemia | |
| 650 | 4 | |a Phenylalanine Metabolite | |
| 650 | 4 | |a Phenyllactic Acid | |
| 650 | 4 | |a Response Type | |
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