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Chronic psychosocial stressors are associated with alterations in salience processing and corticostriatal connectivity

Psychosocial stressors including childhood adversity, migration, and living in an urban environment, have been associated with several psychiatric disorders, including psychotic disorders. The neural and psychological mechanisms mediating this relationship remain unclear. In parallel, alterations in...

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Autores principales: McCutcheon, Robert A., Bloomfield, Michael A.P., Dahoun, Tarik, Mehta, Mitul, Howes, Oliver D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Publisher B. V 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817361/
https://www.ncbi.nlm.nih.gov/pubmed/30573409
http://dx.doi.org/10.1016/j.schres.2018.12.011
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author McCutcheon, Robert A.
Bloomfield, Michael A.P.
Dahoun, Tarik
Mehta, Mitul
Howes, Oliver D.
author_facet McCutcheon, Robert A.
Bloomfield, Michael A.P.
Dahoun, Tarik
Mehta, Mitul
Howes, Oliver D.
author_sort McCutcheon, Robert A.
collection PubMed
description Psychosocial stressors including childhood adversity, migration, and living in an urban environment, have been associated with several psychiatric disorders, including psychotic disorders. The neural and psychological mechanisms mediating this relationship remain unclear. In parallel, alterations in corticostriatal connectivity and abnormalities in the processing of salience, are seen in psychotic disorders. Aberrant functioning of these mechanisms secondary to chronic stress exposure, could help explain how common environmental exposures are associated with a diverse range of symptoms. In the current study, we recruited two groups of adults, one with a high degree of exposure to chronic psychosocial stressors (the exposed group, n = 20), and one with minimal exposure (the unexposed group, n = 22). All participants underwent a resting state MRI scan, completed the Aberrant Salience Inventory, and performed a behavioural task – the Salience Attribution Test (SAT). The exposed group showed reduced explicit adaptive salience scores (cohen's d = 0.69, p = 0.03) and increased aberrant salience inventory scores (d = 0.65, p = 0.04). The exposed group also showed increased corticostriatal connectivity between the ventral striatum and brain regions previously implicated in salience processing. Corticostriatal connectivity in these regions negatively correlated with SAT explicit adaptive salience (r = −0.48, p = 0.001), and positively correlated with aberrant salience inventory scores (r = 0.42, p = 0.006). Furthermore, in a mediation analysis there was tentative evidence that differences in striato-cortical connectivity mediated the group differences in salience scores.
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spelling pubmed-68173612019-11-01 Chronic psychosocial stressors are associated with alterations in salience processing and corticostriatal connectivity McCutcheon, Robert A. Bloomfield, Michael A.P. Dahoun, Tarik Mehta, Mitul Howes, Oliver D. Schizophr Res Article Psychosocial stressors including childhood adversity, migration, and living in an urban environment, have been associated with several psychiatric disorders, including psychotic disorders. The neural and psychological mechanisms mediating this relationship remain unclear. In parallel, alterations in corticostriatal connectivity and abnormalities in the processing of salience, are seen in psychotic disorders. Aberrant functioning of these mechanisms secondary to chronic stress exposure, could help explain how common environmental exposures are associated with a diverse range of symptoms. In the current study, we recruited two groups of adults, one with a high degree of exposure to chronic psychosocial stressors (the exposed group, n = 20), and one with minimal exposure (the unexposed group, n = 22). All participants underwent a resting state MRI scan, completed the Aberrant Salience Inventory, and performed a behavioural task – the Salience Attribution Test (SAT). The exposed group showed reduced explicit adaptive salience scores (cohen's d = 0.69, p = 0.03) and increased aberrant salience inventory scores (d = 0.65, p = 0.04). The exposed group also showed increased corticostriatal connectivity between the ventral striatum and brain regions previously implicated in salience processing. Corticostriatal connectivity in these regions negatively correlated with SAT explicit adaptive salience (r = −0.48, p = 0.001), and positively correlated with aberrant salience inventory scores (r = 0.42, p = 0.006). Furthermore, in a mediation analysis there was tentative evidence that differences in striato-cortical connectivity mediated the group differences in salience scores. Elsevier Science Publisher B. V 2019-11 /pmc/articles/PMC6817361/ /pubmed/30573409 http://dx.doi.org/10.1016/j.schres.2018.12.011 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
McCutcheon, Robert A.
Bloomfield, Michael A.P.
Dahoun, Tarik
Mehta, Mitul
Howes, Oliver D.
Chronic psychosocial stressors are associated with alterations in salience processing and corticostriatal connectivity
title Chronic psychosocial stressors are associated with alterations in salience processing and corticostriatal connectivity
title_full Chronic psychosocial stressors are associated with alterations in salience processing and corticostriatal connectivity
title_fullStr Chronic psychosocial stressors are associated with alterations in salience processing and corticostriatal connectivity
title_full_unstemmed Chronic psychosocial stressors are associated with alterations in salience processing and corticostriatal connectivity
title_short Chronic psychosocial stressors are associated with alterations in salience processing and corticostriatal connectivity
title_sort chronic psychosocial stressors are associated with alterations in salience processing and corticostriatal connectivity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817361/
https://www.ncbi.nlm.nih.gov/pubmed/30573409
http://dx.doi.org/10.1016/j.schres.2018.12.011
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