ABSTRACT
â¢22q11DS offers a compelling model to understand the neural substrates of attentional dysfunction.â¢First study directly comparing neural function in 22q11DS vs. ADHD patientsâ¢22q11DS and ADHD patients show a shared deficit in RI-related activation.â¢ADHD patients showed greater activity in the middle frontal gyrus than 22q11DS during RI.â¢Neural activity is inversely correlated with self-reported Cognitive Impulsivity in 22q11DS.
Subject(s)
Attention Deficit Disorder with Hyperactivity/complications , Brain Mapping , Brain/pathology , DiGeorge Syndrome/complications , Impulsive Behavior/physiology , Inhibition, Psychological , Adolescent , Adult , Analysis of Variance , Attention Deficit Disorder with Hyperactivity/pathology , Brain/blood supply , Female , Follow-Up Studies , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Neuropsychological Tests , Oxygen/blood , Psychiatric Status Rating Scales , Statistics as Topic , Young AdultABSTRACT
22q11.2 deletion syndrome (22q11DS) is associated with elevated levels of impulsivity, inattention, and distractibility, which may be related to underlying neurobiological dysfunction due to haploinsufficiency for genes involved in dopaminergic neurotransmission (i.e. catechol-O-methyltransferase). The Stop-signal task has been employed to probe the neural circuitry involved in response inhibition (RI); findings in healthy individuals indicate that a fronto-basal ganglia network underlies successful inhibition of a prepotent motor response. However, little is known about the neurobiological substrates of RI difficulties in 22q11DS. Here, we investigated this using functional magnetic resonance imaging while 45 adult participants (15 22q11DS patients, 30 matched controls) performed the Stop-signal task. Healthy controls showed significantly greater activation than 22q11DS patients within frontal cortical and basal ganglia regions during successful RI, whereas 22q11DS patients did not show increased neural activity relative to controls in any regions. Using the Barratt Impulsivity Scale, we also investigated whether neural dysfunction during RI was associated with cognitive impulsivity in 22q11DS patients. RI-related activity within left middle frontal gyrus and basal ganglia was associated with severity of self-reported cognitive impulsivity. These results suggest reduced engagement of RI-related brain regions in 22q11DS patients, which may be relevant to characteristic behavioral manifestations of the disorder.
