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Phenylalanine hydroxylase deficiency: Molecular epidemiology and predictable BH4-responsiveness in South Portugal PKU patients
- Source :
- Molecular Genetics and Metabolism. 104:S86-S92
- Publication Year :
- 2011
- Publisher :
- Elsevier BV, 2011.
-
Abstract
- Hyperphenylalaninemia (HPA, OMIM #261600), which includes phenylketonuria (PKU), is caused by mutations in the gene encoding phenylalanine hydroxylase (PAH), being already described more than 600 different mutations. Genotype-phenotype correlation is a useful tool to predict the metabolic phenotype, to establish the better tailored diet and, more recently, to assess the potential responsiveness to BH(4) therapy, a current theme on PKU field. The aim of this study was the molecular analysis of the PAH gene, evaluation of genotype-phenotype relationships and prediction of BH(4)-responsiveness in the HPA population living in South Portugal. We performed the molecular characterization of 83 HPA patients using genomic DNA extracted from peripheral blood samples or Guthrie cards. PAH mutations were scanned by PCR amplification of exons and related intronic boundaries, followed by direct sequence analysis. Intragenic polymorphisms were determined by PCR-RFLP analysis. The results allowed the full characterization of 67 patients. The mutational spectrum encompasses 34 distinct mutations, being the most frequent IVS10nt-11G>A (14.6%), V388M (10.8%), R261Q (8.2%) and R270K (7.6%), which account for 46% of all mutant alleles. Moreover, 12 different haplotypes were identified and most mutations were associated with a single one. Notably, more than half of the 34 mutations belong to the group of more than 70 mutations already identified in BH(4)-responsive patients, according to BIOPKU database. Fifty one different genotypic combinations were found, most of them in single patients and involving a BH(4)-responsive mutation. In conclusion, a significant number (30-35%) of South Portugal PKU patients may potentially benefit from BH(4) therapy which, combined with a less strict diet, or eventually in special cases as monotherapy, may contribute to reduce nutritional deficiencies and minimize neurological and psychological dysfunctions.
- Subjects :
- Phenylalanine hydroxylase
Endocrinology, Diabetes and Metabolism
DNA Mutational Analysis
Population
medicine.disease_cause
Biochemistry
Endocrinology
Hyperphenylalaninemia
Phenylketonurias
Genotype
Genetics
medicine
Humans
Allele
education
Molecular Biology
Genetic Association Studies
Molecular Epidemiology
Mutation
education.field_of_study
Portugal
biology
Molecular epidemiology
Haplotype
Phenylalanine Hydroxylase
medicine.disease
Biopterin
Phenotype
Haplotypes
Child, Preschool
biology.protein
Subjects
Details
- ISSN :
- 10967192
- Volume :
- 104
- Database :
- OpenAIRE
- Journal :
- Molecular Genetics and Metabolism
- Accession number :
- edsair.doi.dedup.....850ad3756e5ea58a92e70ecb4d6a81e6
- Full Text :
- https://doi.org/10.1016/j.ymgme.2011.07.026