Tourette syndrome and dopaminergic genes: A family-based association study in the French Canadian founder population


Por: Díaz-Anzaldúa A., Joober R., Rivière J.-B., Dion Y., Lespérance P., Richer F., Chouinard S., Rouleau G.A.

Publicada: 1 ene 2004
Resumen:
Tourette syndrome (TS) is a genetically complex disorder for which no causative genes have been unequivocally identified. Nevertheless, a number of molecular genetic studies have investigated several candidate genes, particularly those implicated in dopamine modulation. The results of these studies were inconclusive, which may be due, at least in part, to the variable ethnicity of the patients included in different studies and the chosen research design. In this study, we used a family-based association approach to investigate the implication of dopamine-related candidate genes, which had been previously reported as possibly associated with TS [genes that encode for the dopamine receptors DRD2, DRD3 and DRD4, the dopamine transporter 1 (SLC6A3) and the monoamine oxldase-A (MAO-A). The studied group was composed of 110 TS patients. These patients were selected from the French Canadian population, which displays a founder effect. Excess transmission of the 7-repeat allele of the DRD4 exon-3 VNTR polymorphism (?2 TDT =4.93, 1 df, P=0.026) and the putative 'high-activity' alleles of the MAO-A promoter VNTR polymorphism (?2 TDT =7.124, 1 df P=0.0076) were observed. These results were confirmed in a subgroup of patients with no attention deficit/hyperactivity or obsessive compulsive comorbid disorders. Haplotype analysis using one or two supplemental polymorphism in each of these genes confirmed these associations and allowed one to identify risk haplotypes. No associations were found for DRD2, DRD3 or SLC6A3. These data support the notion that DRD4 and MOA-A genes may confer an increased risk for developing TS in the French Canadian population.

Filiaciones:
Díaz-Anzaldúa A.:
 McGill University Health Centre, Montreal, Que., Canada

Joober R.:
 Douglas Hospital Research Centre, Montreal, Que., Canada

Rivière J.-B.:
 McGill University Health Centre, Montreal, Que., Canada

Dion Y.:
 McGill University Health Centre, Montreal, Que., Canada

Lespérance P.:
 Ctr. Hosp. de l'Univ. de Montreal, Montreal, Que., Canada

Richer F.:
 Ctr. Hosp. de l'Univ. de Montreal, Montreal, Que., Canada

Chouinard S.:
 Ctr. Hosp. de l'Univ. de Montreal, Montreal, Que., Canada

 Sainte Justine Hospital, Montreal, Que., Canada

Rouleau G.A.:
 McGill University Health Centre, Montreal, Que., Canada

 McGill University, Health Centre Research Institute, 1650 Cedar Avenue, Montreal, Que. H3G 1A4, Canada
ISSN: 13594184
Editorial
Nature Publishing Group, MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 9 Número: 3
Páginas: 272-277
WOS Id: 000220129200007
ID de PubMed: 15094788
imagen Bronze