Sex-specific influence of DRD2 on ADHD-type temperament in a large population-based birth cohort.

نویسندگان

  • Emma S Nyman
  • Anu Loukola
  • Teppo Varilo
  • Anja Taanila
  • Tuula Hurtig
  • Irma Moilanen
  • Sandra Loo
  • James J McGough
  • Marjo-Riitta Järvelin
  • Susan L Smalley
  • Stanley F Nelson
  • Leena Peltonen
چکیده

Attention-deficit/hyperactivity disorder (ADHD) is a childhood-onset neurodevelopmental disorder with a significant public-health impact. Previously, we described a candidate gene study in a population-based birth cohort that demonstrated an association with ADHD-affected males and the dopamine receptor D2 (DRD2). The current study evaluates potential associations of dopamine receptor genes and Cloninger temperament traits within this same sample. Participants with stringent lifetime ADHD diagnoses were ascertained systematically from the genetically isolated Northern Finland 1986 Birth Cohort (n=9432), resulting in 178 cases and 157 controls. Markers in all known dopamine receptor genes were genotyped. We report an association of DRD2 with low Persistence in females (rs1079727 P=0.02, rs1124491 P=0.02, rs1800497 P=0.03). The associated DRD2 minor allelic haplotype (CAA, P=0.03) is the same haplotype we previously associated with ADHD in males in this birth cohort. The current study further supports previous results on the role of DRD2 in individuals with ADHD. Investigations suggest that DRD2 may have an impact on both males and females, but the particular outcome appears sex-specific, manifesting as ADHD in males and low Persistence in females. Furthermore, these findings suggest that the putative role of low Persistence as an endophenotype for ADHD deserves further investigation.

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عنوان ژورنال:
  • Psychiatric genetics

دوره 22 4  شماره 

صفحات  -

تاریخ انتشار 2012