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Impulsive-antisocial psychopathic traits linked to increased volume and functional connectivity within prefrontal cortex

Psychopathy is a personality disorder characterized by callous lack of empathy, impulsive antisocial behavior, and criminal recidivism. Studies of brain structure and function in psychopathy have frequently identified abnormalities in the prefrontal cortex. However, findings have not yet converged t...

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Autores principales: Korponay, Cole, Pujara, Maia, Deming, Philip, Philippi, Carissa, Decety, Jean, Kosson, David S., Kiehl, Kent A., Koenigs, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490676/
https://www.ncbi.nlm.nih.gov/pubmed/28402565
http://dx.doi.org/10.1093/scan/nsx042
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author Korponay, Cole
Pujara, Maia
Deming, Philip
Philippi, Carissa
Decety, Jean
Kosson, David S.
Kiehl, Kent A.
Koenigs, Michael
author_facet Korponay, Cole
Pujara, Maia
Deming, Philip
Philippi, Carissa
Decety, Jean
Kosson, David S.
Kiehl, Kent A.
Koenigs, Michael
author_sort Korponay, Cole
collection PubMed
description Psychopathy is a personality disorder characterized by callous lack of empathy, impulsive antisocial behavior, and criminal recidivism. Studies of brain structure and function in psychopathy have frequently identified abnormalities in the prefrontal cortex. However, findings have not yet converged to yield a clear relationship between specific subregions of prefrontal cortex and particular psychopathic traits. We performed a multimodal neuroimaging study of prefrontal cortex volume and functional connectivity in psychopathy, using a sample of adult male prison inmates (N = 124). We conducted volumetric analyses in prefrontal subregions, and subsequently assessed resting-state functional connectivity in areas where volume was related to psychopathy severity. We found that overall psychopathy severity and Factor 2 scores (which index the impulsive/antisocial traits of psychopathy) were associated with larger prefrontal subregion volumes, particularly in the medial orbitofrontal cortex and dorsolateral prefrontal cortex. Furthermore, Factor 2 scores were also positively correlated with functional connectivity between several areas of the prefrontal cortex. The results were not attributable to age, race, IQ, substance use history, or brain volume. Collectively, these findings provide evidence for co-localized increases in prefrontal cortex volume and intra-prefrontal functional connectivity in relation to impulsive/antisocial psychopathic traits.
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spelling pubmed-54906762017-07-05 Impulsive-antisocial psychopathic traits linked to increased volume and functional connectivity within prefrontal cortex Korponay, Cole Pujara, Maia Deming, Philip Philippi, Carissa Decety, Jean Kosson, David S. Kiehl, Kent A. Koenigs, Michael Soc Cogn Affect Neurosci Original Articles Psychopathy is a personality disorder characterized by callous lack of empathy, impulsive antisocial behavior, and criminal recidivism. Studies of brain structure and function in psychopathy have frequently identified abnormalities in the prefrontal cortex. However, findings have not yet converged to yield a clear relationship between specific subregions of prefrontal cortex and particular psychopathic traits. We performed a multimodal neuroimaging study of prefrontal cortex volume and functional connectivity in psychopathy, using a sample of adult male prison inmates (N = 124). We conducted volumetric analyses in prefrontal subregions, and subsequently assessed resting-state functional connectivity in areas where volume was related to psychopathy severity. We found that overall psychopathy severity and Factor 2 scores (which index the impulsive/antisocial traits of psychopathy) were associated with larger prefrontal subregion volumes, particularly in the medial orbitofrontal cortex and dorsolateral prefrontal cortex. Furthermore, Factor 2 scores were also positively correlated with functional connectivity between several areas of the prefrontal cortex. The results were not attributable to age, race, IQ, substance use history, or brain volume. Collectively, these findings provide evidence for co-localized increases in prefrontal cortex volume and intra-prefrontal functional connectivity in relation to impulsive/antisocial psychopathic traits. Oxford University Press 2017-04-11 /pmc/articles/PMC5490676/ /pubmed/28402565 http://dx.doi.org/10.1093/scan/nsx042 Text en © The Author(s) (2017). Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Original Articles
Korponay, Cole
Pujara, Maia
Deming, Philip
Philippi, Carissa
Decety, Jean
Kosson, David S.
Kiehl, Kent A.
Koenigs, Michael
Impulsive-antisocial psychopathic traits linked to increased volume and functional connectivity within prefrontal cortex
title Impulsive-antisocial psychopathic traits linked to increased volume and functional connectivity within prefrontal cortex
title_full Impulsive-antisocial psychopathic traits linked to increased volume and functional connectivity within prefrontal cortex
title_fullStr Impulsive-antisocial psychopathic traits linked to increased volume and functional connectivity within prefrontal cortex
title_full_unstemmed Impulsive-antisocial psychopathic traits linked to increased volume and functional connectivity within prefrontal cortex
title_short Impulsive-antisocial psychopathic traits linked to increased volume and functional connectivity within prefrontal cortex
title_sort impulsive-antisocial psychopathic traits linked to increased volume and functional connectivity within prefrontal cortex
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490676/
https://www.ncbi.nlm.nih.gov/pubmed/28402565
http://dx.doi.org/10.1093/scan/nsx042
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