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Mol Genet Metab. 2005 Dec;86 Suppl 1:S67-74. Epub 2005 Sep 28.

Incidence of BH4-responsiveness in phenylalanine-hydroxylase-deficient Italian patients.

Author information

1
Department of Paediatrics, San Paolo Hospital, University of Milan, Italy. l.fiori@libero.it

Abstract

BACKGROUND:

Hyperphenylalaninemia (HPA) is an inherited metabolic disorder due to deficiency of the enzyme phenylalanine hydroxylase (PAH) or its cofactor tetrahydrobiopterin (BH4). BH4-responsiveness in PAH-deficient HPA is a recently described characteristic of most milder phenotypes. BH4-responsive patients show reduction of plasma phenylalanine (phe) levels after oral administration of BH4.

AIM:

Determination of the incidence of BH4-responsiveness among a non-selected, cohort population of PAH-deficient hyperphenylalaninemic patients and evaluation of phenotype-genotype correlations.

PATIENTS AND METHODS:

All patients born in Lombardy (Italy) between January 2000 and December 2004, and affected by HPA (107 patients) were classified after BH4 loading test, analysis of urinary pterins, and determination of DHPR activity in blood, and investigated for BH4-responsiveness. 6R-BH4 (20 mg/kg) was administered orally as a single dose and plasma samples were obtained at time-points 0, 4, 8, and 24 h after BH4 administration. In patients with basal plasma phe levels <or=360 mmol/L a combined phe (100 mg phe/kg) and BH4 (20 mg/kg) loading test was performed. Patients were defined "responsive to BH4" when plasma phe levels decreased by 30% 8h after oral BH4 administration.

RESULTS:

BH4 significantly lowered blood phe levels in 91 (85%) of 107 patients affected by PAH-deficient HPA. Most responsive patients were affected by mild HPA (77%), a smaller percentage by mild (7%) and moderate (7%) phenylketonuria (PKU). One patient with classical PKU was responsive to BH4. Eighteen mutations were found to be associated to the BH4-responsive phenotype.

CONCLUSIONS:

BH4-responsiveness is shown by a consistent number of PAH-deficient hyperphenylalaninemic patients and seems to be common in milder phenotypes. Genotype is not the only factor determining BH4-responsiveness.

PMID:
16198137
DOI:
10.1016/j.ymgme.2005.06.017
[Indexed for MEDLINE]

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