z-logo
Premium
Cognitive functioning in affected sibling pairs with ADHD: familial clustering and dopamine genes
Author(s) -
Loo Sandra K.,
Rich Erika Carpenter,
Ishii Janeen,
McGough James,
McCracken James,
Nelson Stanley,
Smalley Susan L.
Publication year - 2008
Publication title -
journal of child psychology and psychiatry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.652
H-Index - 211
eISSN - 1469-7610
pISSN - 0021-9630
DOI - 10.1111/j.1469-7610.2008.01928.x
Subject(s) - endophenotype , psychology , sibling , cognition , candidate gene , working memory , attention deficit hyperactivity disorder , developmental psychology , clinical psychology , psychiatry , genetics , gene , biology
Background:  This paper examines familiality and candidate gene associations of cognitive measures as potential endophenotypes in attention‐deficit/hyperactivity disorder (ADHD). Methods:  The sample consists of 540 participants, aged 6 to 18, who were diagnosed with ADHD from 251 families recruited for a larger genetic study of ADHD. All members of the family underwent psychiatric interviews and children were administered a large battery of cognitive tasks. Subjects were genotyped for several dopaminergic candidate genes (DAT1, DRD4, and DRD5). Results:  Performance on measures of intelligence, working memory, and set‐shifting had the highest sibling correlations and exhibited significant familial clustering. The 7‐repeat allele of the dopamine receptor D4 (DRD4) gene was associated with poor performance on measures of intelligence, color naming, interference control, and working memory. There were no significant associations with DAT1 and DRD5. Conclusions:  Sibling correlations, familial clustering and candidate gene associations provide strong support for verbal working memory as a candidate endophenotype for ADHD. More complex models of, and larger sample sizes for, genetic association with cognitive functions are encouraged for future study.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here