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Antisocial behavior is associated with reduced frontoparietal network efficiency in youth
Youth antisocial behavior (AB) is associated with deficits in socioemotional processing, reward and threat processing and executive functioning. These deficits are thought to emerge from differences in neural structure, functioning and connectivity, particularly within the default, salience and fron...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275549/ https://www.ncbi.nlm.nih.gov/pubmed/37148314 http://dx.doi.org/10.1093/scan/nsad026 |
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author | Tillem, Scott Dotterer, Hailey L Goetschius, Leigh G Lopez-Duran, Nestor Mitchell, Colter Monk, Christopher S Hyde, Luke W |
author_facet | Tillem, Scott Dotterer, Hailey L Goetschius, Leigh G Lopez-Duran, Nestor Mitchell, Colter Monk, Christopher S Hyde, Luke W |
author_sort | Tillem, Scott |
collection | PubMed |
description | Youth antisocial behavior (AB) is associated with deficits in socioemotional processing, reward and threat processing and executive functioning. These deficits are thought to emerge from differences in neural structure, functioning and connectivity, particularly within the default, salience and frontoparietal networks. However, the relationship between AB and the organization of these networks remains unclear. To address this gap, the current study applied unweighted, undirected graph analyses to resting-state functional magnetic resonance imaging data in a cohort of 161 adolescents (95 female) enriched for exposure to poverty, a risk factor for AB. As prior work indicates that callous-unemotional (CU) traits may moderate the neurocognitive profile of youth AB, we examined CU traits as a moderator. Using multi-informant latent factors, AB was found to be associated with less efficient frontoparietal network topology, a network associated with executive functioning. However, this effect was limited to youth at low or mean levels of CU traits, indicating that these neural differences were specific to those high on AB but not CU traits. Neither AB, CU traits nor their interaction was significantly related to default or salience network topologies. Results suggest that AB, specifically, may be linked with shifts in the architecture of the frontoparietal network. |
format | Online Article Text |
id | pubmed-10275549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102755492023-06-17 Antisocial behavior is associated with reduced frontoparietal network efficiency in youth Tillem, Scott Dotterer, Hailey L Goetschius, Leigh G Lopez-Duran, Nestor Mitchell, Colter Monk, Christopher S Hyde, Luke W Soc Cogn Affect Neurosci Original Manuscript Youth antisocial behavior (AB) is associated with deficits in socioemotional processing, reward and threat processing and executive functioning. These deficits are thought to emerge from differences in neural structure, functioning and connectivity, particularly within the default, salience and frontoparietal networks. However, the relationship between AB and the organization of these networks remains unclear. To address this gap, the current study applied unweighted, undirected graph analyses to resting-state functional magnetic resonance imaging data in a cohort of 161 adolescents (95 female) enriched for exposure to poverty, a risk factor for AB. As prior work indicates that callous-unemotional (CU) traits may moderate the neurocognitive profile of youth AB, we examined CU traits as a moderator. Using multi-informant latent factors, AB was found to be associated with less efficient frontoparietal network topology, a network associated with executive functioning. However, this effect was limited to youth at low or mean levels of CU traits, indicating that these neural differences were specific to those high on AB but not CU traits. Neither AB, CU traits nor their interaction was significantly related to default or salience network topologies. Results suggest that AB, specifically, may be linked with shifts in the architecture of the frontoparietal network. Oxford University Press 2023-05-06 /pmc/articles/PMC10275549/ /pubmed/37148314 http://dx.doi.org/10.1093/scan/nsad026 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Manuscript Tillem, Scott Dotterer, Hailey L Goetschius, Leigh G Lopez-Duran, Nestor Mitchell, Colter Monk, Christopher S Hyde, Luke W Antisocial behavior is associated with reduced frontoparietal network efficiency in youth |
title | Antisocial behavior is associated with reduced frontoparietal network efficiency in youth |
title_full | Antisocial behavior is associated with reduced frontoparietal network efficiency in youth |
title_fullStr | Antisocial behavior is associated with reduced frontoparietal network efficiency in youth |
title_full_unstemmed | Antisocial behavior is associated with reduced frontoparietal network efficiency in youth |
title_short | Antisocial behavior is associated with reduced frontoparietal network efficiency in youth |
title_sort | antisocial behavior is associated with reduced frontoparietal network efficiency in youth |
topic | Original Manuscript |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275549/ https://www.ncbi.nlm.nih.gov/pubmed/37148314 http://dx.doi.org/10.1093/scan/nsad026 |
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