4.8 Article

Inhibition-related modulation of salience and frontoparietal networks predicts cognitive control ability and inattention symptoms in children with ADHD

Journal

MOLECULAR PSYCHIATRY
Volume 26, Issue 8, Pages 4016-4025

Publisher

SPRINGERNATURE
DOI: 10.1038/s41380-019-0564-4

Keywords

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Funding

  1. Brain Resource Company Operations Pty Ltd - National Health and Medical Research Council [APP1008080]
  2. National Institutes of Health [EB022907, NS086085, MH121069, MH105625]
  3. Stanford Departmental Innovator grant
  4. Stanford Children Health Research Institute grant

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Children with ADHD exhibit abnormalities in task-evoked brain connectivity, particularly in the connection between the right dorsolateral prefrontal cortex and posterior parietal cortex. Impairments in the two core cognitive control systems were observed, with connectivity patterns related to NoGo accuracy and severity of inattention symptoms. These findings suggest specific circuit biomarkers for predicting treatment outcomes in childhood ADHD.
Attention-deficit hyperactivity disorder (ADHD) is associated with pervasive impairments in attention and cognitive control. Although brain circuits underlying these impairments have been extensively investigated with resting-state fMRI, little is known about task-evoked functional brain circuits and their relation to cognitive control deficits and inattention symptoms in children with ADHD. Children with ADHD and age, gender and head motion matched typically developing (TD) children completed a Go/NoGo fMRI task. We used multivariate and dimensional analyses to investigate impairments in two core cognitive control systems: (i) cingulo-opercular salience network (SN) anchored in the right anterior insula, dorsal anterior cingulate cortex (rdACC), and ventrolateral prefrontal cortex (rVLPFC) and (ii) dorsal frontoparietal central executive (FPN) network anchored in right dorsolateral prefrontal cortex (rDLPFC) and posterior parietal cortex (rPPC). We found that multivariate patterns of task-evoked effective connectivity between brain regions in SN and FPN distinguished the ADHD and TD groups, with rDLPFC-rPPC connectivity emerging as the most distinguishing link. Task-evoked rdACC-rVLPFC connectivity was positively correlated with NoGo accuracy, and negatively correlated with severity of inattention symptoms. Brain-behavior relationships were robust against potential age, gender, and head motion confounds. Our findings highlight aberrancies in task-evoked modulation of SN and FPN connectivity in children with ADHD. Crucially, cingulo-frontal connectivity was a common locus of deficits in cognitive control and clinical measures of inattention symptoms. Our study provides insights into a parsimonious systems neuroscience model of cognitive control deficits in ADHD, and suggests specific circuit biomarkers for predicting treatment outcomes in childhood ADHD.

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