Article (Published version) (770 Kb) - Limited access to UNIGE
DAT1 and DRD4 genes involved in key dimensions of adult ADHD.
|Published in||Neurological sciences. 2015, vol. 36, no. 6, p. 861-869|
|Abstract||Attention-deficit hyperactivity disorder (ADHD) is a highly heritable neurodevelopmental disorder often persisting in adulthood. Genetic studies of ADHD mainly focused on the Dopamine Transporter (DAT1) and the Dopamine Receptor 4 (DRD4) genes. Nevertheless, polymorphisms of these genes explain only a small fraction of the assigned risk, suggesting that intermediate dimensions and environmental factors should also be considered. We investigated in 77 adult ADHD subjects compared to 474 controls, how polymorphisms within the genes coding for DAT1 (40-bp VNTR in 3'UTR), the Dopamine Receptor 2 (DRD2) (rs1799732) and DRD4 (48-bp VNTR in exon 3), may modulate the expression of the disorder. By genotyping DAT1, we detected a new 9.5R allele showing a deletion of 40 bp and also an insertion of 19 bp compared to the 10R allele. This novel allele was found to be significantly protective for ADHD (p < 0.0001). Another significant difference was found in the distribution of DRD4 48-bp VNTR 6R allele when comparing patients and controls (p = 0.0007). In addition significant results were also found for DAT1 9.5R allele, which was associated with impulsiveness (p = 1.98 × 10(-4)) and trait anger scores (p = 7.66 × 10(-4)). Moreover, impulsiveness scores were partly modulated by an interaction between the DRD4 48-bp VNTR 6R allele and childhood maltreatment (p = 0.01), however, this result did not resist correction for multiple comparisons. Altogether, our results show the putative involvement of DAT1 and DRD4 genes in the aetiology of ADHD with a main role in modulation of key dimensions of the disorder.|
|Research groups||Groupe Giannakopoulos Panteleimon (psychiatrie générale) (201)|
Thérapeutiques des Troubles de l'Humeur et Anxieux (689)
|HASLER, Roland et al. DAT1 and DRD4 genes involved in key dimensions of adult ADHD. In: Neurological sciences, 2015, vol. 36, n° 6, p. 861-869. doi: 10.1007/s10072-014-2051-7 https://archive-ouverte.unige.ch/unige:77145|