Title of article
Activation in Ventral Prefrontal Cortex is Sensitive to Genetic Vulnerability for Attention-Deficit Hyperactivity Disorder
Author/Authors
Sarah Durston، نويسنده , , Martijn Mulder، نويسنده , , B.J. Casey، نويسنده , , Tim Ziermans، نويسنده , , HERMAN VAN ENGELAND، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2006
Pages
9
From page
1062
To page
1070
Abstract
Background
Attention-deficit hyperactivity disorder (ADHD) is a heritable neuropsychiatric disorder, associated with atypical patterns of brain activation in functional imaging studies. Neuroimaging measures may serve as an intermediate phenotype in genetic studies of ADHD, as they are putatively more closely linked to gene expression than a clinical diagnosis.
Methods
We used rapid, mixed-trial, event-related functional magnetic resonance imaging (fMRI) to investigate changes in brain activation during a go no-go task in boys with ADHD, their unaffected siblings, and matched control subjects.
Results
On the hardest inhibitory trials in our task, children and adolescents with ADHD had lower accuracy than control subjects, whereas their unaffected siblings did not. Control subjects activated a network of regions, including ventral prefrontal and inferior parietal cortex. Both children and adolescents with ADHD and their unaffected siblings showed decreased activation in these areas, as well as fewer correlations between performance and activation.
Conclusions
These findings suggest that the magnitude of activation during successful inhibitions is sensitive to genetic vulnerability for ADHD in a number of regions, including ventral prefrontal cortex. If this can be replicated in future studies, this suggests that neuroimaging measures related to inhibitory control may be suitable as intermediate phenotypes in studies investigating gene effects in ADHD
Keywords
ADHD , fMRI , genetic vulnerability , Siblings , ventral PFC , Endophenotype
Journal title
Biological Psychiatry
Serial Year
2006
Journal title
Biological Psychiatry
Record number
503156
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