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Towards a mechanistic understanding of the role of error monitoring and memory in social anxiety

Cognitive models state social anxiety (SA) involves biased cognitive processing that impacts what is learned and remembered within social situations, leading to the maintenance of SA. Neuroscience work links SA to enhanced error monitoring, reflected in error-related neural responses arising from me...

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Autores principales: Hosseini, Kianoosh, Pettit, Jeremy W., Soto, Fabian A., Mattfeld, Aaron T., Buzzell, George A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515949/
https://www.ncbi.nlm.nih.gov/pubmed/37745333
http://dx.doi.org/10.1101/2023.09.14.557662
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author Hosseini, Kianoosh
Pettit, Jeremy W.
Soto, Fabian A.
Mattfeld, Aaron T.
Buzzell, George A.
author_facet Hosseini, Kianoosh
Pettit, Jeremy W.
Soto, Fabian A.
Mattfeld, Aaron T.
Buzzell, George A.
author_sort Hosseini, Kianoosh
collection PubMed
description Cognitive models state social anxiety (SA) involves biased cognitive processing that impacts what is learned and remembered within social situations, leading to the maintenance of SA. Neuroscience work links SA to enhanced error monitoring, reflected in error-related neural responses arising from mediofrontal cortex (MFC). Yet, the role of error monitoring in SA remains unclear, as it is unknown whether error monitoring can drive changes in memory, biasing what is learned or remembered about social situations. Thus, we developed a novel paradigm to investigate the role of error-related MFC theta oscillations (associated with error monitoring) and memory biases in SA. EEG was collected while participants completed a novel Face-Flanker task, involving presentation of task-unrelated, trial-unique faces behind target/flanker arrows on each trial. A subsequent incidental memory assessment evaluated memory biases for error events. Severity of SA symptoms were associated with greater error-related theta synchrony over MFC, as well as between MFC and sensory cortex. SA was positively associated with memory biases for error events. Consistent with a mechanistic role in biased cognitive processing, greater error-related MFC-sensory theta synchrony during the Face-Flanker predicted subsequent memory biases for error events. Our findings suggest high SA individuals exhibit memory biases for error events, and that this behavioral phenomenon may be driven by error-related MFC-sensory theta synchrony associated with error monitoring. Moreover, results demonstrate the potential of a novel paradigm to elucidate mechanisms underlying relations between error monitoring and SA.
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spelling pubmed-105159492023-09-23 Towards a mechanistic understanding of the role of error monitoring and memory in social anxiety Hosseini, Kianoosh Pettit, Jeremy W. Soto, Fabian A. Mattfeld, Aaron T. Buzzell, George A. bioRxiv Article Cognitive models state social anxiety (SA) involves biased cognitive processing that impacts what is learned and remembered within social situations, leading to the maintenance of SA. Neuroscience work links SA to enhanced error monitoring, reflected in error-related neural responses arising from mediofrontal cortex (MFC). Yet, the role of error monitoring in SA remains unclear, as it is unknown whether error monitoring can drive changes in memory, biasing what is learned or remembered about social situations. Thus, we developed a novel paradigm to investigate the role of error-related MFC theta oscillations (associated with error monitoring) and memory biases in SA. EEG was collected while participants completed a novel Face-Flanker task, involving presentation of task-unrelated, trial-unique faces behind target/flanker arrows on each trial. A subsequent incidental memory assessment evaluated memory biases for error events. Severity of SA symptoms were associated with greater error-related theta synchrony over MFC, as well as between MFC and sensory cortex. SA was positively associated with memory biases for error events. Consistent with a mechanistic role in biased cognitive processing, greater error-related MFC-sensory theta synchrony during the Face-Flanker predicted subsequent memory biases for error events. Our findings suggest high SA individuals exhibit memory biases for error events, and that this behavioral phenomenon may be driven by error-related MFC-sensory theta synchrony associated with error monitoring. Moreover, results demonstrate the potential of a novel paradigm to elucidate mechanisms underlying relations between error monitoring and SA. Cold Spring Harbor Laboratory 2023-09-15 /pmc/articles/PMC10515949/ /pubmed/37745333 http://dx.doi.org/10.1101/2023.09.14.557662 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Hosseini, Kianoosh
Pettit, Jeremy W.
Soto, Fabian A.
Mattfeld, Aaron T.
Buzzell, George A.
Towards a mechanistic understanding of the role of error monitoring and memory in social anxiety
title Towards a mechanistic understanding of the role of error monitoring and memory in social anxiety
title_full Towards a mechanistic understanding of the role of error monitoring and memory in social anxiety
title_fullStr Towards a mechanistic understanding of the role of error monitoring and memory in social anxiety
title_full_unstemmed Towards a mechanistic understanding of the role of error monitoring and memory in social anxiety
title_short Towards a mechanistic understanding of the role of error monitoring and memory in social anxiety
title_sort towards a mechanistic understanding of the role of error monitoring and memory in social anxiety
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10515949/
https://www.ncbi.nlm.nih.gov/pubmed/37745333
http://dx.doi.org/10.1101/2023.09.14.557662
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