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Atypical functional connectivity in adolescents and adults with persistent and remitted ADHD during a cognitive control task
We previously provided initial evidence for cognitive and event-related potential markers of persistence/remission of attention-deficit/hyperactivity disorder (ADHD) from childhood to adolescence and adulthood. Here, using a novel brain-network connectivity approach, we aimed to examine whether task...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461684/ https://www.ncbi.nlm.nih.gov/pubmed/30979865 http://dx.doi.org/10.1038/s41398-019-0469-7 |
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author | Michelini, Giorgia Jurgiel, Joseph Bakolis, Ioannis Cheung, Celeste H. M. Asherson, Philip Loo, Sandra K. Kuntsi, Jonna Mohammad-Rezazadeh, Iman |
author_facet | Michelini, Giorgia Jurgiel, Joseph Bakolis, Ioannis Cheung, Celeste H. M. Asherson, Philip Loo, Sandra K. Kuntsi, Jonna Mohammad-Rezazadeh, Iman |
author_sort | Michelini, Giorgia |
collection | PubMed |
description | We previously provided initial evidence for cognitive and event-related potential markers of persistence/remission of attention-deficit/hyperactivity disorder (ADHD) from childhood to adolescence and adulthood. Here, using a novel brain-network connectivity approach, we aimed to examine whether task-based functional connectivity reflects a marker of ADHD remission or an enduring deficit unrelated to ADHD outcome. High-density EEG was recorded in a follow-up of 110 adolescents and young adults with childhood ADHD (87 persisters, 23 remitters) and 169 typically developing individuals during an arrow-flanker task, eliciting cognitive control. Functional connectivity was quantified with network-based graph-theory metrics before incongruent (high-conflict) target onset (pre-stimulus), during target processing (post-stimulus) and in the degree of change between pre-stimulus/post-stimulus. ADHD outcome was examined with parent-reported symptoms and impairment using both a categorical (DSM-IV) and a dimensional approach. Graph-theory measures converged in indicating that, compared to controls, ADHD persisters showed increased connectivity in pre-stimulus theta, alpha, and beta and in post-stimulus beta (all p < .01) and reduced pre-stimulus/post-stimulus change in theta connectivity (p < .01). In the majority of indices showing ADHD persister–control differences, ADHD remitters differed from controls (all p < .05) but not from persisters. Similarly, connectivity measures were unrelated to continuous outcome measures of ADHD symptoms and impairment in participants with childhood ADHD. These findings indicate that adolescents and young adults with persistent and remitted ADHD share atypical over-connectivity profiles and reduced ability to modulate connectivity patterns with task demands, compared to controls. Task-based functional connectivity impairments may represent enduring deficits in individuals with childhood ADHD irrespective of diagnostic status in adolescence/young adulthood. |
format | Online Article Text |
id | pubmed-6461684 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64616842019-04-16 Atypical functional connectivity in adolescents and adults with persistent and remitted ADHD during a cognitive control task Michelini, Giorgia Jurgiel, Joseph Bakolis, Ioannis Cheung, Celeste H. M. Asherson, Philip Loo, Sandra K. Kuntsi, Jonna Mohammad-Rezazadeh, Iman Transl Psychiatry Article We previously provided initial evidence for cognitive and event-related potential markers of persistence/remission of attention-deficit/hyperactivity disorder (ADHD) from childhood to adolescence and adulthood. Here, using a novel brain-network connectivity approach, we aimed to examine whether task-based functional connectivity reflects a marker of ADHD remission or an enduring deficit unrelated to ADHD outcome. High-density EEG was recorded in a follow-up of 110 adolescents and young adults with childhood ADHD (87 persisters, 23 remitters) and 169 typically developing individuals during an arrow-flanker task, eliciting cognitive control. Functional connectivity was quantified with network-based graph-theory metrics before incongruent (high-conflict) target onset (pre-stimulus), during target processing (post-stimulus) and in the degree of change between pre-stimulus/post-stimulus. ADHD outcome was examined with parent-reported symptoms and impairment using both a categorical (DSM-IV) and a dimensional approach. Graph-theory measures converged in indicating that, compared to controls, ADHD persisters showed increased connectivity in pre-stimulus theta, alpha, and beta and in post-stimulus beta (all p < .01) and reduced pre-stimulus/post-stimulus change in theta connectivity (p < .01). In the majority of indices showing ADHD persister–control differences, ADHD remitters differed from controls (all p < .05) but not from persisters. Similarly, connectivity measures were unrelated to continuous outcome measures of ADHD symptoms and impairment in participants with childhood ADHD. These findings indicate that adolescents and young adults with persistent and remitted ADHD share atypical over-connectivity profiles and reduced ability to modulate connectivity patterns with task demands, compared to controls. Task-based functional connectivity impairments may represent enduring deficits in individuals with childhood ADHD irrespective of diagnostic status in adolescence/young adulthood. Nature Publishing Group UK 2019-04-12 /pmc/articles/PMC6461684/ /pubmed/30979865 http://dx.doi.org/10.1038/s41398-019-0469-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Michelini, Giorgia Jurgiel, Joseph Bakolis, Ioannis Cheung, Celeste H. M. Asherson, Philip Loo, Sandra K. Kuntsi, Jonna Mohammad-Rezazadeh, Iman Atypical functional connectivity in adolescents and adults with persistent and remitted ADHD during a cognitive control task |
title | Atypical functional connectivity in adolescents and adults with persistent and remitted ADHD during a cognitive control task |
title_full | Atypical functional connectivity in adolescents and adults with persistent and remitted ADHD during a cognitive control task |
title_fullStr | Atypical functional connectivity in adolescents and adults with persistent and remitted ADHD during a cognitive control task |
title_full_unstemmed | Atypical functional connectivity in adolescents and adults with persistent and remitted ADHD during a cognitive control task |
title_short | Atypical functional connectivity in adolescents and adults with persistent and remitted ADHD during a cognitive control task |
title_sort | atypical functional connectivity in adolescents and adults with persistent and remitted adhd during a cognitive control task |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6461684/ https://www.ncbi.nlm.nih.gov/pubmed/30979865 http://dx.doi.org/10.1038/s41398-019-0469-7 |
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