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Triple Network Model Dynamically Revisited: Lower Salience Network State Switching in Pre-psychosis

Emerging evidence has attributed altered network coordination between the default mode, central executive, and salience networks (DMN/CEN/SAL) to disturbances seen in schizophrenia, but little is known for at-risk psychosis stages. Moreover, pinpointing impairments in specific network-to-network int...

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Autores principales: Bolton, Thomas A. W., Wotruba, Diana, Buechler, Roman, Theodoridou, Anastasia, Michels, Lars, Kollias, Spyros, Rössler, Wulf, Heekeren, Karsten, Van De Ville, Dimitri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027374/
https://www.ncbi.nlm.nih.gov/pubmed/32116776
http://dx.doi.org/10.3389/fphys.2020.00066
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author Bolton, Thomas A. W.
Wotruba, Diana
Buechler, Roman
Theodoridou, Anastasia
Michels, Lars
Kollias, Spyros
Rössler, Wulf
Heekeren, Karsten
Van De Ville, Dimitri
author_facet Bolton, Thomas A. W.
Wotruba, Diana
Buechler, Roman
Theodoridou, Anastasia
Michels, Lars
Kollias, Spyros
Rössler, Wulf
Heekeren, Karsten
Van De Ville, Dimitri
author_sort Bolton, Thomas A. W.
collection PubMed
description Emerging evidence has attributed altered network coordination between the default mode, central executive, and salience networks (DMN/CEN/SAL) to disturbances seen in schizophrenia, but little is known for at-risk psychosis stages. Moreover, pinpointing impairments in specific network-to-network interactions, although essential to resolve possibly distinct harbingers of conversion to clinically diagnosed schizophrenia, remains particularly challenging. We addressed this by a dynamic approach to functional connectivity, where right anterior insula brain interactions were examined through co-activation pattern (CAP) analysis. We utilized resting-state fMRI in 19 subjects suffering from subthreshold delusions and hallucinations (UHR), 28 at-risk for psychosis with basic symptoms describing only self-experienced subclinical disturbances (BS), and 29 healthy controls (CTR) matched for age, gender, handedness, and intelligence. We extracted the most recurring CAPs, compared their relative occurrence and average dwell time to probe their temporal expression, and quantified occurrence balance to assess the putative loss of competing relationships. Our findings substantiate the pivotal role of the right anterior insula in governing CEN-to-DMN transitions, which appear dysfunctional prior to the onset of psychosis, especially when first attenuated psychotic symptoms occur. In UHR subjects, it is longer active in concert with the DMN and there is a loss of competition between a SAL/DMN state, and a state with insula/CEN activation paralleled by DMN deactivation. These features suggest that abnormal network switching disrupts one's capacity to distinguish between the internal world and external environment, which is accompanied by inflexibility and an excessive awareness to internal processes reflected by prolonged expression of the right anterior insula-default mode co-activation pattern.
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spelling pubmed-70273742020-02-28 Triple Network Model Dynamically Revisited: Lower Salience Network State Switching in Pre-psychosis Bolton, Thomas A. W. Wotruba, Diana Buechler, Roman Theodoridou, Anastasia Michels, Lars Kollias, Spyros Rössler, Wulf Heekeren, Karsten Van De Ville, Dimitri Front Physiol Physiology Emerging evidence has attributed altered network coordination between the default mode, central executive, and salience networks (DMN/CEN/SAL) to disturbances seen in schizophrenia, but little is known for at-risk psychosis stages. Moreover, pinpointing impairments in specific network-to-network interactions, although essential to resolve possibly distinct harbingers of conversion to clinically diagnosed schizophrenia, remains particularly challenging. We addressed this by a dynamic approach to functional connectivity, where right anterior insula brain interactions were examined through co-activation pattern (CAP) analysis. We utilized resting-state fMRI in 19 subjects suffering from subthreshold delusions and hallucinations (UHR), 28 at-risk for psychosis with basic symptoms describing only self-experienced subclinical disturbances (BS), and 29 healthy controls (CTR) matched for age, gender, handedness, and intelligence. We extracted the most recurring CAPs, compared their relative occurrence and average dwell time to probe their temporal expression, and quantified occurrence balance to assess the putative loss of competing relationships. Our findings substantiate the pivotal role of the right anterior insula in governing CEN-to-DMN transitions, which appear dysfunctional prior to the onset of psychosis, especially when first attenuated psychotic symptoms occur. In UHR subjects, it is longer active in concert with the DMN and there is a loss of competition between a SAL/DMN state, and a state with insula/CEN activation paralleled by DMN deactivation. These features suggest that abnormal network switching disrupts one's capacity to distinguish between the internal world and external environment, which is accompanied by inflexibility and an excessive awareness to internal processes reflected by prolonged expression of the right anterior insula-default mode co-activation pattern. Frontiers Media S.A. 2020-02-11 /pmc/articles/PMC7027374/ /pubmed/32116776 http://dx.doi.org/10.3389/fphys.2020.00066 Text en Copyright © 2020 Bolton, Wotruba, Buechler, Theodoridou, Michels, Kollias, Rössler, Heekeren and Van De Ville. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Bolton, Thomas A. W.
Wotruba, Diana
Buechler, Roman
Theodoridou, Anastasia
Michels, Lars
Kollias, Spyros
Rössler, Wulf
Heekeren, Karsten
Van De Ville, Dimitri
Triple Network Model Dynamically Revisited: Lower Salience Network State Switching in Pre-psychosis
title Triple Network Model Dynamically Revisited: Lower Salience Network State Switching in Pre-psychosis
title_full Triple Network Model Dynamically Revisited: Lower Salience Network State Switching in Pre-psychosis
title_fullStr Triple Network Model Dynamically Revisited: Lower Salience Network State Switching in Pre-psychosis
title_full_unstemmed Triple Network Model Dynamically Revisited: Lower Salience Network State Switching in Pre-psychosis
title_short Triple Network Model Dynamically Revisited: Lower Salience Network State Switching in Pre-psychosis
title_sort triple network model dynamically revisited: lower salience network state switching in pre-psychosis
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027374/
https://www.ncbi.nlm.nih.gov/pubmed/32116776
http://dx.doi.org/10.3389/fphys.2020.00066
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