Response of patients with phenylketonuria in the US to tetrahydrobiopterin

Reuben Matalon, Kimberlee Michals-Matalon, Richard Koch, James Grady, Stephen Tyring, Raymond C. Stevens

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Tetrahydrobiopterin (BH4) responsive forms of phenylketonuria (PKU) have been recognized since 1999. Subsequent studies have shown that patients with PKU, especially those with mild mutations, respond with lower blood phenylalanine (Phe) concentrations following oral administration of 6-r-l-erythro-5, 6, 7, 8-tetrahydrobiopterin (BH4). To determine the incidence of BH4 responding PKU patients in the United States and characterize their phenylalanine hydroxylase (PAH) mutations, a study was undertaken at UTMB in Galveston and the Children's Hospital of Los Angeles on 38 patients with PKU. Patients were screened by a single oral dose of BH 4, 10 mg/kg and blood Phe and tyrosine were determined at 0, 4, 8, and 24 h. Twenty-two individuals (58%) responded with marked decrease in blood Phe (>30%) at 24 h. Some of the patients that responded favourably were clinically described as having Classical PKU. Blood tyrosine concentrations did not change significantly. Twenty subjects with PKU, responsive and non-responsive to BH4, were enrolled in a second study to evaluate blood Phe response to ascending single doses of BH4 with 10, 20, and 40 mg/kg and to evaluate multiple daily doses, for 7 days each, with 10 and 20 mg/kg BH4. The 7-day trial showed a sustained decrease in blood Phe in 14 of 20 patients taking 20 mg/kg BH4 (70%). Of these 14 patients, 10 (71%) responded with a significant decrease in blood Phe following 10 mg/kg BH4 daily. To understand the mechanism of response to BH4, the kinetics and stability of mutant PAH were studied. We found that mutant PAH responds with increase in the residual enzyme activity following BH4 administration. The increase in activity is multi-factorial caused by increased stability, chaperone effect, and correction of the mutant Km. These studies indicate that BH4 can be of help to patients with PKU, including some considered to have Classical PKU. The PKU population in US is heterogeneous and mutations can be varied so mutations need to be characterized and response to BH4 tested. It is more likely that mutations with residual activity should respond to BH4, therefore the clinical definition of "Classical PKU" should be reconciled with the residual activity of PAH mutations.

Original languageEnglish (US)
JournalMolecular Genetics and Metabolism
Volume86
Issue numberSUPPL.
DOIs
StatePublished - Dec 2005

Fingerprint

Phenylketonurias
Phenylalanine
Phenylalanine Hydroxylase
Blood
Mutation
Tyrosine
Enzyme activity
sapropterin
Los Angeles
Oral Administration
Kinetics

Keywords

  • BH
  • BH kinetic studies
  • Phenylketonuria
  • PKU
  • Tetrahydrobiopterin

ASJC Scopus subject areas

  • Biochemistry
  • Genetics
  • Endocrinology, Diabetes and Metabolism

Cite this

Response of patients with phenylketonuria in the US to tetrahydrobiopterin. / Matalon, Reuben; Michals-Matalon, Kimberlee; Koch, Richard; Grady, James; Tyring, Stephen; Stevens, Raymond C.

In: Molecular Genetics and Metabolism, Vol. 86, No. SUPPL., 12.2005.

Research output: Contribution to journalArticle

Matalon, Reuben ; Michals-Matalon, Kimberlee ; Koch, Richard ; Grady, James ; Tyring, Stephen ; Stevens, Raymond C. / Response of patients with phenylketonuria in the US to tetrahydrobiopterin. In: Molecular Genetics and Metabolism. 2005 ; Vol. 86, No. SUPPL.
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abstract = "Tetrahydrobiopterin (BH4) responsive forms of phenylketonuria (PKU) have been recognized since 1999. Subsequent studies have shown that patients with PKU, especially those with mild mutations, respond with lower blood phenylalanine (Phe) concentrations following oral administration of 6-r-l-erythro-5, 6, 7, 8-tetrahydrobiopterin (BH4). To determine the incidence of BH4 responding PKU patients in the United States and characterize their phenylalanine hydroxylase (PAH) mutations, a study was undertaken at UTMB in Galveston and the Children's Hospital of Los Angeles on 38 patients with PKU. Patients were screened by a single oral dose of BH 4, 10 mg/kg and blood Phe and tyrosine were determined at 0, 4, 8, and 24 h. Twenty-two individuals (58{\%}) responded with marked decrease in blood Phe (>30{\%}) at 24 h. Some of the patients that responded favourably were clinically described as having Classical PKU. Blood tyrosine concentrations did not change significantly. Twenty subjects with PKU, responsive and non-responsive to BH4, were enrolled in a second study to evaluate blood Phe response to ascending single doses of BH4 with 10, 20, and 40 mg/kg and to evaluate multiple daily doses, for 7 days each, with 10 and 20 mg/kg BH4. The 7-day trial showed a sustained decrease in blood Phe in 14 of 20 patients taking 20 mg/kg BH4 (70{\%}). Of these 14 patients, 10 (71{\%}) responded with a significant decrease in blood Phe following 10 mg/kg BH4 daily. To understand the mechanism of response to BH4, the kinetics and stability of mutant PAH were studied. We found that mutant PAH responds with increase in the residual enzyme activity following BH4 administration. The increase in activity is multi-factorial caused by increased stability, chaperone effect, and correction of the mutant Km. These studies indicate that BH4 can be of help to patients with PKU, including some considered to have Classical PKU. The PKU population in US is heterogeneous and mutations can be varied so mutations need to be characterized and response to BH4 tested. It is more likely that mutations with residual activity should respond to BH4, therefore the clinical definition of {"}Classical PKU{"} should be reconciled with the residual activity of PAH mutations.",
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