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Inhibition-related modulation of salience and fronto-parietal networks predicts cognitive control ability and inattention symptoms in children with 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 an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188596/ https://www.ncbi.nlm.nih.gov/pubmed/31664176 http://dx.doi.org/10.1038/s41380-019-0564-4 |
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author | Cai, Weidong Griffiths, Kristi Korgaonkar, Mayuresh S. Williams, Leanne Maree Menon, Vinod |
author_facet | Cai, Weidong Griffiths, Kristi Korgaonkar, Mayuresh S. Williams, Leanne Maree Menon, Vinod |
author_sort | Cai, Weidong |
collection | PubMed |
description | 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 fronto-parietal “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 control 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. |
format | Online Article Text |
id | pubmed-7188596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71885962021-04-29 Inhibition-related modulation of salience and fronto-parietal networks predicts cognitive control ability and inattention symptoms in children with ADHD Cai, Weidong Griffiths, Kristi Korgaonkar, Mayuresh S. Williams, Leanne Maree Menon, Vinod Mol Psychiatry Article 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 fronto-parietal “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 control 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. 2019-10-29 2021-08 /pmc/articles/PMC7188596/ /pubmed/31664176 http://dx.doi.org/10.1038/s41380-019-0564-4 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Cai, Weidong Griffiths, Kristi Korgaonkar, Mayuresh S. Williams, Leanne Maree Menon, Vinod Inhibition-related modulation of salience and fronto-parietal networks predicts cognitive control ability and inattention symptoms in children with ADHD |
title | Inhibition-related modulation of salience and fronto-parietal networks predicts cognitive control ability and inattention symptoms in children with ADHD |
title_full | Inhibition-related modulation of salience and fronto-parietal networks predicts cognitive control ability and inattention symptoms in children with ADHD |
title_fullStr | Inhibition-related modulation of salience and fronto-parietal networks predicts cognitive control ability and inattention symptoms in children with ADHD |
title_full_unstemmed | Inhibition-related modulation of salience and fronto-parietal networks predicts cognitive control ability and inattention symptoms in children with ADHD |
title_short | Inhibition-related modulation of salience and fronto-parietal networks predicts cognitive control ability and inattention symptoms in children with ADHD |
title_sort | inhibition-related modulation of salience and fronto-parietal networks predicts cognitive control ability and inattention symptoms in children with adhd |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188596/ https://www.ncbi.nlm.nih.gov/pubmed/31664176 http://dx.doi.org/10.1038/s41380-019-0564-4 |
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