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Brain system segregation and pain catastrophizing in chronic pain progression

Pain processing involves emotional and cognitive factors that can modify pain perception. Increasing evidence suggests that pain catastrophizing (PC) is implicated, through pain-related self-thoughts, in the maladaptive plastic changes related to the maintenance of chronic pain (CP). Functional magn...

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Autores principales: Delgado-Gallén, Selma, Soler, MD, Cabello-Toscano, María, Abellaneda-Pérez, Kilian, Solana-Sánchez, Javier, España-Irla, Goretti, Roca-Ventura, Alba, Bartrés-Faz, David, Tormos, Josep M., Pascual-Leone, Alvaro, Cattaneo, Gabriele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060861/
https://www.ncbi.nlm.nih.gov/pubmed/37008229
http://dx.doi.org/10.3389/fnins.2023.1148176
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author Delgado-Gallén, Selma
Soler, MD
Cabello-Toscano, María
Abellaneda-Pérez, Kilian
Solana-Sánchez, Javier
España-Irla, Goretti
Roca-Ventura, Alba
Bartrés-Faz, David
Tormos, Josep M.
Pascual-Leone, Alvaro
Cattaneo, Gabriele
author_facet Delgado-Gallén, Selma
Soler, MD
Cabello-Toscano, María
Abellaneda-Pérez, Kilian
Solana-Sánchez, Javier
España-Irla, Goretti
Roca-Ventura, Alba
Bartrés-Faz, David
Tormos, Josep M.
Pascual-Leone, Alvaro
Cattaneo, Gabriele
author_sort Delgado-Gallén, Selma
collection PubMed
description Pain processing involves emotional and cognitive factors that can modify pain perception. Increasing evidence suggests that pain catastrophizing (PC) is implicated, through pain-related self-thoughts, in the maladaptive plastic changes related to the maintenance of chronic pain (CP). Functional magnetic resonance imaging (fMRI) studies have shown an association between CP and two main networks: default mode (DMN) and dorsoattentional (DAN). Brain system segregation degree (SyS), an fMRI framework used to quantify the extent to which functional networks are segregated from each other, is associated with cognitive abilities in both healthy individuals and neurological patients. We hypothesized that individuals suffering from CP would show worst health-related status compared to healthy individuals and that, within CP individuals, longitudinal changes in pain experience (pain intensity and affective interference), could be predicted by SyS and PC subdomains (rumination, magnification, and helplessness). To assess the longitudinal progression of CP, two pain surveys were taken before and after an in-person assessment (physical evaluation and fMRI). We first compared the sociodemographic, health-related, and SyS data in the whole sample (no pain and pain groups). Secondly, we ran linear regression and a moderation model only in the pain group, to see the predictive and moderator values of PC and SyS in pain progression. From our sample of 347 individuals (mean age = 53.84, 55.2% women), 133 responded to having CP, and 214 denied having CP. When comparing groups, results showed significant differences in health-related questionnaires, but no differences in SyS. Within the pain group, helplessness (β = 0.325; p = 0.003), higher DMN (β = 0.193; p = 0.037), and lower DAN segregation (β = 0.215; p = 0.014) were strongly associated with a worsening in pain experience over time. Moreover, helplessness moderated the association between DMN segregation and pain experience progression (p = 0.003). Our findings indicate that the efficient functioning of these networks and catastrophizing could be used as predictors of pain progression, bringing new light to the influence of the interplay between psychological aspects and brain networks. Consequently, approaches focusing on these factors could minimize the impact on daily life activities.
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spelling pubmed-100608612023-03-31 Brain system segregation and pain catastrophizing in chronic pain progression Delgado-Gallén, Selma Soler, MD Cabello-Toscano, María Abellaneda-Pérez, Kilian Solana-Sánchez, Javier España-Irla, Goretti Roca-Ventura, Alba Bartrés-Faz, David Tormos, Josep M. Pascual-Leone, Alvaro Cattaneo, Gabriele Front Neurosci Neuroscience Pain processing involves emotional and cognitive factors that can modify pain perception. Increasing evidence suggests that pain catastrophizing (PC) is implicated, through pain-related self-thoughts, in the maladaptive plastic changes related to the maintenance of chronic pain (CP). Functional magnetic resonance imaging (fMRI) studies have shown an association between CP and two main networks: default mode (DMN) and dorsoattentional (DAN). Brain system segregation degree (SyS), an fMRI framework used to quantify the extent to which functional networks are segregated from each other, is associated with cognitive abilities in both healthy individuals and neurological patients. We hypothesized that individuals suffering from CP would show worst health-related status compared to healthy individuals and that, within CP individuals, longitudinal changes in pain experience (pain intensity and affective interference), could be predicted by SyS and PC subdomains (rumination, magnification, and helplessness). To assess the longitudinal progression of CP, two pain surveys were taken before and after an in-person assessment (physical evaluation and fMRI). We first compared the sociodemographic, health-related, and SyS data in the whole sample (no pain and pain groups). Secondly, we ran linear regression and a moderation model only in the pain group, to see the predictive and moderator values of PC and SyS in pain progression. From our sample of 347 individuals (mean age = 53.84, 55.2% women), 133 responded to having CP, and 214 denied having CP. When comparing groups, results showed significant differences in health-related questionnaires, but no differences in SyS. Within the pain group, helplessness (β = 0.325; p = 0.003), higher DMN (β = 0.193; p = 0.037), and lower DAN segregation (β = 0.215; p = 0.014) were strongly associated with a worsening in pain experience over time. Moreover, helplessness moderated the association between DMN segregation and pain experience progression (p = 0.003). Our findings indicate that the efficient functioning of these networks and catastrophizing could be used as predictors of pain progression, bringing new light to the influence of the interplay between psychological aspects and brain networks. Consequently, approaches focusing on these factors could minimize the impact on daily life activities. Frontiers Media S.A. 2023-03-16 /pmc/articles/PMC10060861/ /pubmed/37008229 http://dx.doi.org/10.3389/fnins.2023.1148176 Text en Copyright © 2023 Delgado-Gallén, Soler, Cabello-Toscano, Abellaneda-Pérez, Solana-Sánchez, España-Irla, Roca-Ventura, Bartrés-Faz, Tormos, Pascual-Leone and Cattaneo. https://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
Delgado-Gallén, Selma
Soler, MD
Cabello-Toscano, María
Abellaneda-Pérez, Kilian
Solana-Sánchez, Javier
España-Irla, Goretti
Roca-Ventura, Alba
Bartrés-Faz, David
Tormos, Josep M.
Pascual-Leone, Alvaro
Cattaneo, Gabriele
Brain system segregation and pain catastrophizing in chronic pain progression
title Brain system segregation and pain catastrophizing in chronic pain progression
title_full Brain system segregation and pain catastrophizing in chronic pain progression
title_fullStr Brain system segregation and pain catastrophizing in chronic pain progression
title_full_unstemmed Brain system segregation and pain catastrophizing in chronic pain progression
title_short Brain system segregation and pain catastrophizing in chronic pain progression
title_sort brain system segregation and pain catastrophizing in chronic pain progression
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10060861/
https://www.ncbi.nlm.nih.gov/pubmed/37008229
http://dx.doi.org/10.3389/fnins.2023.1148176
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