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Pharmacokinetics of tetrahydrobiopterin following oral loadings with three single dosages in patients with phenylketonuria


Gramer, G; Garbade, S F; Blau, N; Lindner, M (2009). Pharmacokinetics of tetrahydrobiopterin following oral loadings with three single dosages in patients with phenylketonuria. Journal of Inherited Metabolic Disease, 32(1):52-57.

Abstract

BACKGROUND: Tetrahydrobiopterin (BH(4)) loading has been performed for many years in patients detected by newborn screening for hyperphenylalaninaemia (HPA) to distinguish BH(4) cofactor synthesis or recycling defects from phenylalanine hydroxylase (PAH)-deficient HPA. Previous studies have shown that the pharmacokinetics of BH(4) shows high intra-individual and inter-individual variability. METHODS: Seventeen adult patients with PAH-deficient HPA were classified in one of three phenotypic groups (mild, moderate, classical PKU) according to their response to a standardized protein loading test. Genotype information was available for all participants. In a randomized controlled double-blind design, BH(4) loadings in single oral dosages of 10, 20 and 30 mg BH(4)/kg body weight (bw) were performed to assess BH(4) responsiveness. As part of this study, levels of BH(4) metabolites in dried blood spots were studied to provide information on the pharmacokinetics of BH(4) following oral administration. RESULTS: Levels of biopterin and pterin (B + P) increased significantly with increasing BH(4) dose (p < 0.0001). Maximum B + P levels were reached 4 hours after application of BH(4). There was no significant difference in BH(4) pharmacokinetics between the three phenotypic groups of PKU. Male and female patients showed different levels of BH(4) metabolites following 10 mg BH(4)/kg bw, but not following 20 and 30 mg BH(4)/kg bw. There was no relationship between age of patients and BH(4) pharmacokinetics. There was no correlation between B + P levels and decrease in Phe level (p = 0.69). CONCLUSION: BH(4) pharmacokinetics are variable between patients regarding absolute levels of BH(4) metabolites reached after BH(4) loading, but are similar regarding the interval to individual maximum B + P levels. Levels of B + P increase significantly with increasing BH(4) doses. There is no correlation between B + P levels and decrease in Phe level.

Abstract

BACKGROUND: Tetrahydrobiopterin (BH(4)) loading has been performed for many years in patients detected by newborn screening for hyperphenylalaninaemia (HPA) to distinguish BH(4) cofactor synthesis or recycling defects from phenylalanine hydroxylase (PAH)-deficient HPA. Previous studies have shown that the pharmacokinetics of BH(4) shows high intra-individual and inter-individual variability. METHODS: Seventeen adult patients with PAH-deficient HPA were classified in one of three phenotypic groups (mild, moderate, classical PKU) according to their response to a standardized protein loading test. Genotype information was available for all participants. In a randomized controlled double-blind design, BH(4) loadings in single oral dosages of 10, 20 and 30 mg BH(4)/kg body weight (bw) were performed to assess BH(4) responsiveness. As part of this study, levels of BH(4) metabolites in dried blood spots were studied to provide information on the pharmacokinetics of BH(4) following oral administration. RESULTS: Levels of biopterin and pterin (B + P) increased significantly with increasing BH(4) dose (p < 0.0001). Maximum B + P levels were reached 4 hours after application of BH(4). There was no significant difference in BH(4) pharmacokinetics between the three phenotypic groups of PKU. Male and female patients showed different levels of BH(4) metabolites following 10 mg BH(4)/kg bw, but not following 20 and 30 mg BH(4)/kg bw. There was no relationship between age of patients and BH(4) pharmacokinetics. There was no correlation between B + P levels and decrease in Phe level (p = 0.69). CONCLUSION: BH(4) pharmacokinetics are variable between patients regarding absolute levels of BH(4) metabolites reached after BH(4) loading, but are similar regarding the interval to individual maximum B + P levels. Levels of B + P increase significantly with increasing BH(4) doses. There is no correlation between B + P levels and decrease in Phe level.

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Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:04 Faculty of Medicine > University Children's Hospital Zurich > Medical Clinic
Dewey Decimal Classification:610 Medicine & health
Language:English
Date:2009
Deposited On:04 Jan 2010 11:36
Last Modified:05 Apr 2016 13:41
Publisher:Springer
ISSN:0141-8955
Additional Information:The original publication is available at www.springerlink.com
Publisher DOI:https://doi.org/10.1007/s10545-008-0955-1
PubMed ID:19016342

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