Cargando…

Childhood trauma, IL-6 and weaker suppression of the default mode network (DMN) during theory of mind (ToM) performance in schizophrenia

BACKGROUND: Both low-grade systemic inflammation and functional connectivity of the default mode network (DMN) during rest have recently been observed to mediate the association between childhood trauma (CT) and behavioural performance on an emotion recognition task. Whether inflammation also mediat...

Descripción completa

Detalles Bibliográficos
Autores principales: King, Sinead, Mothersill, David, Holleran, Laurena, Patlola, Saahithh, McManus, Ross, Kenyon, Marcus, McDonald, Colm, Hallahan, Brian, Corvin, Aiden, Morris, Derek W., Kelly, John P., McKernan, Declan, Donohoe, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640308/
https://www.ncbi.nlm.nih.gov/pubmed/36388137
http://dx.doi.org/10.1016/j.bbih.2022.100540
_version_ 1784825818883555328
author King, Sinead
Mothersill, David
Holleran, Laurena
Patlola, Saahithh
McManus, Ross
Kenyon, Marcus
McDonald, Colm
Hallahan, Brian
Corvin, Aiden
Morris, Derek W.
Kelly, John P.
McKernan, Declan
Donohoe, Gary
author_facet King, Sinead
Mothersill, David
Holleran, Laurena
Patlola, Saahithh
McManus, Ross
Kenyon, Marcus
McDonald, Colm
Hallahan, Brian
Corvin, Aiden
Morris, Derek W.
Kelly, John P.
McKernan, Declan
Donohoe, Gary
author_sort King, Sinead
collection PubMed
description BACKGROUND: Both low-grade systemic inflammation and functional connectivity of the default mode network (DMN) during rest have recently been observed to mediate the association between childhood trauma (CT) and behavioural performance on an emotion recognition task. Whether inflammation also mediates the association between CT and functional connectivity of the DMN during social cognitive task performance is unknown. METHODS: 51 patients with schizophrenia (SZ) or schizoaffective disorder (SZA) and 176 healthy participants completed a theory of mind (ToM) task during fMRI. IL-6 was measured in plasma using ELISA. DMN connectivity was measured during performance of the fMRI ToM task. To examine DMN connectivity, we selected 4 a priori seeds of the DMN, i.e., the medial prefrontal cortex (PFC), right lateral parietal (LP), left LP, and posterior cingulate cortex (PCC) according to the Harvard-Oxford Cortical and Subcortical Atlas (http://www.cma.mgh.harvard.edu/fsl_atlas.html) as implemented in CONN. RESULTS: Patients showed significantly increased DMN connectivity compared to healthy participants between each of the four seeds of the DMN and with other clusters in the brain. Across the entire sample, higher levels of IL-6 predicted increased connectivity between the mPFC and regions encompassing the cerebellum (<0.001 FWE). IL-6 mediated the association between physical neglect and weaker suppression of the posterior cingulate cortex (PCC) DMN seed -left precentral and postcentral gyrus (β(INDIRECT) = .0170, CI: 0.0008 to.0506) connectivity during ToM performance. DISCUSSION: This is the first study to our knowledge that provides evidence that higher plasma IL-6 mediates the association between higher childhood neglect and increased DMN connectivity during ToM task performance. Consistent with our previous study that IL-6 mediated the association between early life stress exposure and reduced connectivity of the DMN during rest, here IL-6 mediated the association between early life stress and increased connectivity of the DMN during ToM based cognitive processing. These findings suggest a biological mechanism for how chronic stress impacts social cognitive processing.
format Online
Article
Text
id pubmed-9640308
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-96403082022-11-15 Childhood trauma, IL-6 and weaker suppression of the default mode network (DMN) during theory of mind (ToM) performance in schizophrenia King, Sinead Mothersill, David Holleran, Laurena Patlola, Saahithh McManus, Ross Kenyon, Marcus McDonald, Colm Hallahan, Brian Corvin, Aiden Morris, Derek W. Kelly, John P. McKernan, Declan Donohoe, Gary Brain Behav Immun Health Full Length Article BACKGROUND: Both low-grade systemic inflammation and functional connectivity of the default mode network (DMN) during rest have recently been observed to mediate the association between childhood trauma (CT) and behavioural performance on an emotion recognition task. Whether inflammation also mediates the association between CT and functional connectivity of the DMN during social cognitive task performance is unknown. METHODS: 51 patients with schizophrenia (SZ) or schizoaffective disorder (SZA) and 176 healthy participants completed a theory of mind (ToM) task during fMRI. IL-6 was measured in plasma using ELISA. DMN connectivity was measured during performance of the fMRI ToM task. To examine DMN connectivity, we selected 4 a priori seeds of the DMN, i.e., the medial prefrontal cortex (PFC), right lateral parietal (LP), left LP, and posterior cingulate cortex (PCC) according to the Harvard-Oxford Cortical and Subcortical Atlas (http://www.cma.mgh.harvard.edu/fsl_atlas.html) as implemented in CONN. RESULTS: Patients showed significantly increased DMN connectivity compared to healthy participants between each of the four seeds of the DMN and with other clusters in the brain. Across the entire sample, higher levels of IL-6 predicted increased connectivity between the mPFC and regions encompassing the cerebellum (<0.001 FWE). IL-6 mediated the association between physical neglect and weaker suppression of the posterior cingulate cortex (PCC) DMN seed -left precentral and postcentral gyrus (β(INDIRECT) = .0170, CI: 0.0008 to.0506) connectivity during ToM performance. DISCUSSION: This is the first study to our knowledge that provides evidence that higher plasma IL-6 mediates the association between higher childhood neglect and increased DMN connectivity during ToM task performance. Consistent with our previous study that IL-6 mediated the association between early life stress exposure and reduced connectivity of the DMN during rest, here IL-6 mediated the association between early life stress and increased connectivity of the DMN during ToM based cognitive processing. These findings suggest a biological mechanism for how chronic stress impacts social cognitive processing. Elsevier 2022-10-27 /pmc/articles/PMC9640308/ /pubmed/36388137 http://dx.doi.org/10.1016/j.bbih.2022.100540 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Full Length Article
King, Sinead
Mothersill, David
Holleran, Laurena
Patlola, Saahithh
McManus, Ross
Kenyon, Marcus
McDonald, Colm
Hallahan, Brian
Corvin, Aiden
Morris, Derek W.
Kelly, John P.
McKernan, Declan
Donohoe, Gary
Childhood trauma, IL-6 and weaker suppression of the default mode network (DMN) during theory of mind (ToM) performance in schizophrenia
title Childhood trauma, IL-6 and weaker suppression of the default mode network (DMN) during theory of mind (ToM) performance in schizophrenia
title_full Childhood trauma, IL-6 and weaker suppression of the default mode network (DMN) during theory of mind (ToM) performance in schizophrenia
title_fullStr Childhood trauma, IL-6 and weaker suppression of the default mode network (DMN) during theory of mind (ToM) performance in schizophrenia
title_full_unstemmed Childhood trauma, IL-6 and weaker suppression of the default mode network (DMN) during theory of mind (ToM) performance in schizophrenia
title_short Childhood trauma, IL-6 and weaker suppression of the default mode network (DMN) during theory of mind (ToM) performance in schizophrenia
title_sort childhood trauma, il-6 and weaker suppression of the default mode network (dmn) during theory of mind (tom) performance in schizophrenia
topic Full Length Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640308/
https://www.ncbi.nlm.nih.gov/pubmed/36388137
http://dx.doi.org/10.1016/j.bbih.2022.100540
work_keys_str_mv AT kingsinead childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT mothersilldavid childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT holleranlaurena childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT patlolasaahithh childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT mcmanusross childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT kenyonmarcus childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT mcdonaldcolm childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT hallahanbrian childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT corvinaiden childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT morrisderekw childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT kellyjohnp childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT mckernandeclan childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia
AT donohoegary childhoodtraumail6andweakersuppressionofthedefaultmodenetworkdmnduringtheoryofmindtomperformanceinschizophrenia