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Altered Sensory Insular Connectivity in Chronic Postsurgical Pain Patients

Chronic postsurgical pain (CPSP) occurs in up to 50% of individuals after surgeries and 32% after hysterectomy, leading to major adverse effects on quality of life and socioeconomic burden. Little is known about whether and how large-scale neural networks being affected in CPSP, particularly with re...

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Autores principales: Ching, Yin Ying, Wang, Chenhao, Tay, Terence, Loke, Yng Miin, Tang, Phua Hwee, Sng, Ban Leong, Zhou, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290251/
https://www.ncbi.nlm.nih.gov/pubmed/30568586
http://dx.doi.org/10.3389/fnhum.2018.00483
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author Ching, Yin Ying
Wang, Chenhao
Tay, Terence
Loke, Yng Miin
Tang, Phua Hwee
Sng, Ban Leong
Zhou, Juan
author_facet Ching, Yin Ying
Wang, Chenhao
Tay, Terence
Loke, Yng Miin
Tang, Phua Hwee
Sng, Ban Leong
Zhou, Juan
author_sort Ching, Yin Ying
collection PubMed
description Chronic postsurgical pain (CPSP) occurs in up to 50% of individuals after surgeries and 32% after hysterectomy, leading to major adverse effects on quality of life and socioeconomic burden. Little is known about whether and how large-scale neural networks being affected in CPSP, particularly with regard to the functional connectivity (FC) of insula which is known to be the hub of the intrinsic neural network playing a critical role in pain processing. Here, we sought to examine the dynamics of insular FC in the context of noxious stimuli in CPSP patients. To this aim, resting state fMRI data were acquired, before and after acute heat pain stimulation, from 11 individuals with chronic post-hysterectomy pain (CPHP) and 22 age-matched healthy controls (HCs) who had a hysterectomy but without chronic post-surgical pain. We examined whole-brain FC were mapped by seeding at the sensorimotor and chemosensory subfields of the insula and found significant group × stimulation interaction effects. Specifically, the HC group had increased FC between the left sensorimotor insula and right angular and middle occipital gyrus (MOG) and increased FC between the left chemosensory insula and bilateral angular and MOG following pain stimulation. In contrast, such pain stimulation related FC changes were absent in the CPHP group. Furthermore, higher insular FC at baseline and smaller increased insular FC after pain stimulation correlated with clinical pain scores in CPHP patients. Our findings suggest that CPSP is associated with altered dynamics of large-scale functional networks anchored in the insula.
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spelling pubmed-62902512018-12-19 Altered Sensory Insular Connectivity in Chronic Postsurgical Pain Patients Ching, Yin Ying Wang, Chenhao Tay, Terence Loke, Yng Miin Tang, Phua Hwee Sng, Ban Leong Zhou, Juan Front Hum Neurosci Neuroscience Chronic postsurgical pain (CPSP) occurs in up to 50% of individuals after surgeries and 32% after hysterectomy, leading to major adverse effects on quality of life and socioeconomic burden. Little is known about whether and how large-scale neural networks being affected in CPSP, particularly with regard to the functional connectivity (FC) of insula which is known to be the hub of the intrinsic neural network playing a critical role in pain processing. Here, we sought to examine the dynamics of insular FC in the context of noxious stimuli in CPSP patients. To this aim, resting state fMRI data were acquired, before and after acute heat pain stimulation, from 11 individuals with chronic post-hysterectomy pain (CPHP) and 22 age-matched healthy controls (HCs) who had a hysterectomy but without chronic post-surgical pain. We examined whole-brain FC were mapped by seeding at the sensorimotor and chemosensory subfields of the insula and found significant group × stimulation interaction effects. Specifically, the HC group had increased FC between the left sensorimotor insula and right angular and middle occipital gyrus (MOG) and increased FC between the left chemosensory insula and bilateral angular and MOG following pain stimulation. In contrast, such pain stimulation related FC changes were absent in the CPHP group. Furthermore, higher insular FC at baseline and smaller increased insular FC after pain stimulation correlated with clinical pain scores in CPHP patients. Our findings suggest that CPSP is associated with altered dynamics of large-scale functional networks anchored in the insula. Frontiers Media S.A. 2018-12-05 /pmc/articles/PMC6290251/ /pubmed/30568586 http://dx.doi.org/10.3389/fnhum.2018.00483 Text en Copyright © 2018 Ching, Wang, Tay, Loke, Tang, Sng and Zhou. 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 Neuroscience
Ching, Yin Ying
Wang, Chenhao
Tay, Terence
Loke, Yng Miin
Tang, Phua Hwee
Sng, Ban Leong
Zhou, Juan
Altered Sensory Insular Connectivity in Chronic Postsurgical Pain Patients
title Altered Sensory Insular Connectivity in Chronic Postsurgical Pain Patients
title_full Altered Sensory Insular Connectivity in Chronic Postsurgical Pain Patients
title_fullStr Altered Sensory Insular Connectivity in Chronic Postsurgical Pain Patients
title_full_unstemmed Altered Sensory Insular Connectivity in Chronic Postsurgical Pain Patients
title_short Altered Sensory Insular Connectivity in Chronic Postsurgical Pain Patients
title_sort altered sensory insular connectivity in chronic postsurgical pain patients
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290251/
https://www.ncbi.nlm.nih.gov/pubmed/30568586
http://dx.doi.org/10.3389/fnhum.2018.00483
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