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A multilevel examination of lifetime aggression: integrating cortical thickness, personality pathology and trauma exposure

Aggression represents a significant public health concern, causing serious physical and psychological harm. Although many studies have sought to characterize the etiology of aggression, research on the contributions of risk factors that span multiple levels of analysis for explaining aggressive beha...

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Autores principales: Sheehan, Ana E, Bounoua, Nadia, Miglin, Rickie, Spielberg, Jeffrey M, Sadeh, Naomi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259263/
https://www.ncbi.nlm.nih.gov/pubmed/33837772
http://dx.doi.org/10.1093/scan/nsab042
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author Sheehan, Ana E
Bounoua, Nadia
Miglin, Rickie
Spielberg, Jeffrey M
Sadeh, Naomi
author_facet Sheehan, Ana E
Bounoua, Nadia
Miglin, Rickie
Spielberg, Jeffrey M
Sadeh, Naomi
author_sort Sheehan, Ana E
collection PubMed
description Aggression represents a significant public health concern, causing serious physical and psychological harm. Although many studies have sought to characterize the etiology of aggression, research on the contributions of risk factors that span multiple levels of analysis for explaining aggressive behavior is lacking. To address this gap, we investigated the direct and unique contributions of cortical thickness (level 1), pathological personality traits (level 2) and trauma exposure (level 3) for explaining lifetime physical aggression in a high-risk sample of community adults (N = 129, 47.3% men). First, the frequency of lifetime aggression was inversely associated with cortical thickness in regions of prefrontal and temporal cortices that have been implicated in executive functioning, inhibitory mechanisms and socio-emotional processing. Further, aggression was positively associated with pathological personality traits (antagonism and disinhibition) and exposure to assaultive trauma. Notably, all three levels of analysis (cortical thickness, pathological personality traits and assaultive trauma exposure) explained non-overlapping variance in aggressive behavior when examined simultaneously in integrative models. Together, the findings provide a multilevel assessment of the biopsychosocial factors associated with the frequency of aggression. They also indicate that cortical thickness explains novel variance in these harmful behaviors not captured by well-established personality and environmental risk factors for aggression.
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spelling pubmed-82592632021-07-07 A multilevel examination of lifetime aggression: integrating cortical thickness, personality pathology and trauma exposure Sheehan, Ana E Bounoua, Nadia Miglin, Rickie Spielberg, Jeffrey M Sadeh, Naomi Soc Cogn Affect Neurosci Original Manuscript Aggression represents a significant public health concern, causing serious physical and psychological harm. Although many studies have sought to characterize the etiology of aggression, research on the contributions of risk factors that span multiple levels of analysis for explaining aggressive behavior is lacking. To address this gap, we investigated the direct and unique contributions of cortical thickness (level 1), pathological personality traits (level 2) and trauma exposure (level 3) for explaining lifetime physical aggression in a high-risk sample of community adults (N = 129, 47.3% men). First, the frequency of lifetime aggression was inversely associated with cortical thickness in regions of prefrontal and temporal cortices that have been implicated in executive functioning, inhibitory mechanisms and socio-emotional processing. Further, aggression was positively associated with pathological personality traits (antagonism and disinhibition) and exposure to assaultive trauma. Notably, all three levels of analysis (cortical thickness, pathological personality traits and assaultive trauma exposure) explained non-overlapping variance in aggressive behavior when examined simultaneously in integrative models. Together, the findings provide a multilevel assessment of the biopsychosocial factors associated with the frequency of aggression. They also indicate that cortical thickness explains novel variance in these harmful behaviors not captured by well-established personality and environmental risk factors for aggression. Oxford University Press 2021-04-10 /pmc/articles/PMC8259263/ /pubmed/33837772 http://dx.doi.org/10.1093/scan/nsab042 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Manuscript
Sheehan, Ana E
Bounoua, Nadia
Miglin, Rickie
Spielberg, Jeffrey M
Sadeh, Naomi
A multilevel examination of lifetime aggression: integrating cortical thickness, personality pathology and trauma exposure
title A multilevel examination of lifetime aggression: integrating cortical thickness, personality pathology and trauma exposure
title_full A multilevel examination of lifetime aggression: integrating cortical thickness, personality pathology and trauma exposure
title_fullStr A multilevel examination of lifetime aggression: integrating cortical thickness, personality pathology and trauma exposure
title_full_unstemmed A multilevel examination of lifetime aggression: integrating cortical thickness, personality pathology and trauma exposure
title_short A multilevel examination of lifetime aggression: integrating cortical thickness, personality pathology and trauma exposure
title_sort multilevel examination of lifetime aggression: integrating cortical thickness, personality pathology and trauma exposure
topic Original Manuscript
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259263/
https://www.ncbi.nlm.nih.gov/pubmed/33837772
http://dx.doi.org/10.1093/scan/nsab042
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