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Early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (DMN) during face processing in Schizophrenia

Childhood trauma (CT) is associated with lower cognitive and social cognitive function in schizophrenia. Recent evidence suggests that the relationship between CT and cognition is mediated by both low-grade systemic inflammation and reduced connectivity of the default mode network (DMN) during resti...

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Autores principales: King, Sinead, Mothersill, David, Holleran, Laurena, Patlola, Saahithh Redddi, Burke, Tom, McManus, Ross, Kenyon, Marcus, McDonald, Colm, Hallahan, Brian, Corvin, Aiden, Morris, Derek W., Kelly, John P., McKernan, Declan P., Donohoe, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282071/
https://www.ncbi.nlm.nih.gov/pubmed/37339948
http://dx.doi.org/10.1038/s41398-023-02512-4
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author King, Sinead
Mothersill, David
Holleran, Laurena
Patlola, Saahithh Redddi
Burke, Tom
McManus, Ross
Kenyon, Marcus
McDonald, Colm
Hallahan, Brian
Corvin, Aiden
Morris, Derek W.
Kelly, John P.
McKernan, Declan P.
Donohoe, Gary
author_facet King, Sinead
Mothersill, David
Holleran, Laurena
Patlola, Saahithh Redddi
Burke, Tom
McManus, Ross
Kenyon, Marcus
McDonald, Colm
Hallahan, Brian
Corvin, Aiden
Morris, Derek W.
Kelly, John P.
McKernan, Declan P.
Donohoe, Gary
author_sort King, Sinead
collection PubMed
description Childhood trauma (CT) is associated with lower cognitive and social cognitive function in schizophrenia. Recent evidence suggests that the relationship between CT and cognition is mediated by both low-grade systemic inflammation and reduced connectivity of the default mode network (DMN) during resting state. This study sought to test whether the same pattern of associations was observed for DMN connectivity during task based activity. Fifty-three individuals with schizophrenia (SZ) or schizoaffective disorder (SZA) and one hundred and seventy six healthy participants were recruited from the Immune Response and Social Cognition (iRELATE) project. A panel of pro-inflammatory markers that included IL-6, IL-8, IL-10, tumour necrosis factor-alpha (TNFa), and C-reactive protein (CRP), were measured in plasma using ELISA. DMN connectivity was measured during an fMRI social cognitive face processing task. Patients showed evidence of low grade systemic inflammation and significantly increased connectivity between the left lateral parietal (LLP) cortex-cerebellum and LLP-left angular gyrus compared to healthy participants. Across the entire sample, IL-6 predicted increased connectivity between LLP-cerebellum, LLP-precuneus, and mPFC-bilateral-precentral-gyri and left postcentral gyrus. In turn, and again in the entire sample, IL-6 (but no other inflammatory marker) mediated the relationship between childhood physical neglect and LLP-cerebellum. Physical neglect scores also significantly predicted the positive association between IL-6 and LLP-precuneus connectivity. This is to our knowledge the first study that provides evidence that higher plasma IL-6 mediates the association between higher childhood neglect and increased DMN connectivity during task based activity. Consistent with our hypothesis, exposure to trauma is associated with weaker suppression of the DMN during a face processing task, and this association was mediated via increased inflammatory response. The findings may represent part of the biological mechanism by which CT and cognitive performance are related.
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spelling pubmed-102820712023-06-22 Early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (DMN) during face processing in Schizophrenia King, Sinead Mothersill, David Holleran, Laurena Patlola, Saahithh Redddi Burke, Tom McManus, Ross Kenyon, Marcus McDonald, Colm Hallahan, Brian Corvin, Aiden Morris, Derek W. Kelly, John P. McKernan, Declan P. Donohoe, Gary Transl Psychiatry Article Childhood trauma (CT) is associated with lower cognitive and social cognitive function in schizophrenia. Recent evidence suggests that the relationship between CT and cognition is mediated by both low-grade systemic inflammation and reduced connectivity of the default mode network (DMN) during resting state. This study sought to test whether the same pattern of associations was observed for DMN connectivity during task based activity. Fifty-three individuals with schizophrenia (SZ) or schizoaffective disorder (SZA) and one hundred and seventy six healthy participants were recruited from the Immune Response and Social Cognition (iRELATE) project. A panel of pro-inflammatory markers that included IL-6, IL-8, IL-10, tumour necrosis factor-alpha (TNFa), and C-reactive protein (CRP), were measured in plasma using ELISA. DMN connectivity was measured during an fMRI social cognitive face processing task. Patients showed evidence of low grade systemic inflammation and significantly increased connectivity between the left lateral parietal (LLP) cortex-cerebellum and LLP-left angular gyrus compared to healthy participants. Across the entire sample, IL-6 predicted increased connectivity between LLP-cerebellum, LLP-precuneus, and mPFC-bilateral-precentral-gyri and left postcentral gyrus. In turn, and again in the entire sample, IL-6 (but no other inflammatory marker) mediated the relationship between childhood physical neglect and LLP-cerebellum. Physical neglect scores also significantly predicted the positive association between IL-6 and LLP-precuneus connectivity. This is to our knowledge the first study that provides evidence that higher plasma IL-6 mediates the association between higher childhood neglect and increased DMN connectivity during task based activity. Consistent with our hypothesis, exposure to trauma is associated with weaker suppression of the DMN during a face processing task, and this association was mediated via increased inflammatory response. The findings may represent part of the biological mechanism by which CT and cognitive performance are related. Nature Publishing Group UK 2023-06-21 /pmc/articles/PMC10282071/ /pubmed/37339948 http://dx.doi.org/10.1038/s41398-023-02512-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
King, Sinead
Mothersill, David
Holleran, Laurena
Patlola, Saahithh Redddi
Burke, Tom
McManus, Ross
Kenyon, Marcus
McDonald, Colm
Hallahan, Brian
Corvin, Aiden
Morris, Derek W.
Kelly, John P.
McKernan, Declan P.
Donohoe, Gary
Early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (DMN) during face processing in Schizophrenia
title Early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (DMN) during face processing in Schizophrenia
title_full Early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (DMN) during face processing in Schizophrenia
title_fullStr Early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (DMN) during face processing in Schizophrenia
title_full_unstemmed Early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (DMN) during face processing in Schizophrenia
title_short Early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (DMN) during face processing in Schizophrenia
title_sort early life stress, low-grade systemic inflammation and weaker suppression of the default mode network (dmn) during face processing in schizophrenia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10282071/
https://www.ncbi.nlm.nih.gov/pubmed/37339948
http://dx.doi.org/10.1038/s41398-023-02512-4
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