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Altered connectivity of the right anterior insula drives the pain connectome changes in chronic knee osteoarthritis

Resting-state functional connectivity (FC) has proven a powerful approach to understand the neural underpinnings of chronic pain, reporting altered connectivity in 3 main networks: the default mode network (DMN), central executive network, and the salience network (SN). The interrelation and possibl...

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Autores principales: Cottam, William J., Iwabuchi, Sarina J., Drabek, Marianne M., Reckziegel, Diane, Auer, Dorothee P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916486/
https://www.ncbi.nlm.nih.gov/pubmed/29557928
http://dx.doi.org/10.1097/j.pain.0000000000001209
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author Cottam, William J.
Iwabuchi, Sarina J.
Drabek, Marianne M.
Reckziegel, Diane
Auer, Dorothee P.
author_facet Cottam, William J.
Iwabuchi, Sarina J.
Drabek, Marianne M.
Reckziegel, Diane
Auer, Dorothee P.
author_sort Cottam, William J.
collection PubMed
description Resting-state functional connectivity (FC) has proven a powerful approach to understand the neural underpinnings of chronic pain, reporting altered connectivity in 3 main networks: the default mode network (DMN), central executive network, and the salience network (SN). The interrelation and possible mechanisms of these changes are less well understood in chronic pain. Based on emerging evidence of its role to drive switches between network states, the right anterior insula (rAI, an SN hub) may play a dominant role in network connectivity changes underpinning chronic pain. To test this hypothesis, we used seed-based resting-state FC analysis including dynamic and effective connectivity metrics in 25 people with chronic osteoarthritis (OA) pain and 19 matched healthy volunteers. Compared with controls, participants with painful knee OA presented with increased anticorrelation between the rAI (SN) and DMN regions. Also, the left dorsal prefrontal cortex (central executive network hub) showed more negative FC with the right temporal gyrus. Granger causality analysis revealed increased negative influence of the rAI on the posterior cingulate (DMN) in patients with OA in line with the observed enhanced anticorrelation. Moreover, dynamic FC was lower in the DMN of patients and thus more similar to temporal dynamics of the SN. Together, these findings evidence a widespread network disruption in patients with persistent OA pain and point toward a driving role of the rAI.
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spelling pubmed-59164862018-05-02 Altered connectivity of the right anterior insula drives the pain connectome changes in chronic knee osteoarthritis Cottam, William J. Iwabuchi, Sarina J. Drabek, Marianne M. Reckziegel, Diane Auer, Dorothee P. Pain Research Paper Resting-state functional connectivity (FC) has proven a powerful approach to understand the neural underpinnings of chronic pain, reporting altered connectivity in 3 main networks: the default mode network (DMN), central executive network, and the salience network (SN). The interrelation and possible mechanisms of these changes are less well understood in chronic pain. Based on emerging evidence of its role to drive switches between network states, the right anterior insula (rAI, an SN hub) may play a dominant role in network connectivity changes underpinning chronic pain. To test this hypothesis, we used seed-based resting-state FC analysis including dynamic and effective connectivity metrics in 25 people with chronic osteoarthritis (OA) pain and 19 matched healthy volunteers. Compared with controls, participants with painful knee OA presented with increased anticorrelation between the rAI (SN) and DMN regions. Also, the left dorsal prefrontal cortex (central executive network hub) showed more negative FC with the right temporal gyrus. Granger causality analysis revealed increased negative influence of the rAI on the posterior cingulate (DMN) in patients with OA in line with the observed enhanced anticorrelation. Moreover, dynamic FC was lower in the DMN of patients and thus more similar to temporal dynamics of the SN. Together, these findings evidence a widespread network disruption in patients with persistent OA pain and point toward a driving role of the rAI. Wolters Kluwer 2018-03-16 2018-05 /pmc/articles/PMC5916486/ /pubmed/29557928 http://dx.doi.org/10.1097/j.pain.0000000000001209 Text en Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the International Association for the Study of Pain. This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Cottam, William J.
Iwabuchi, Sarina J.
Drabek, Marianne M.
Reckziegel, Diane
Auer, Dorothee P.
Altered connectivity of the right anterior insula drives the pain connectome changes in chronic knee osteoarthritis
title Altered connectivity of the right anterior insula drives the pain connectome changes in chronic knee osteoarthritis
title_full Altered connectivity of the right anterior insula drives the pain connectome changes in chronic knee osteoarthritis
title_fullStr Altered connectivity of the right anterior insula drives the pain connectome changes in chronic knee osteoarthritis
title_full_unstemmed Altered connectivity of the right anterior insula drives the pain connectome changes in chronic knee osteoarthritis
title_short Altered connectivity of the right anterior insula drives the pain connectome changes in chronic knee osteoarthritis
title_sort altered connectivity of the right anterior insula drives the pain connectome changes in chronic knee osteoarthritis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5916486/
https://www.ncbi.nlm.nih.gov/pubmed/29557928
http://dx.doi.org/10.1097/j.pain.0000000000001209
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