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Altered functional connectivity associated with time discounting in chronic pain
Chronic pain (CP) is a global problem extensively associated with an unhealthy lifestyle. Time discounting (TD), a tendency to assign less value to future gains than to present gains, is an indicator of the unhealthy behaviors. While, recent neuroimaging studies implied overlapping neuro mechanisms...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544657/ https://www.ncbi.nlm.nih.gov/pubmed/31148557 http://dx.doi.org/10.1038/s41598-019-44497-5 |
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author | Wakaizumi, Kenta Jabakhanji, Rami Ihara, Naho Kosugi, Shizuko Terasawa, Yuri Morisaki, Hiroshi Ogaki, Masao Baliki, Marwan N. |
author_facet | Wakaizumi, Kenta Jabakhanji, Rami Ihara, Naho Kosugi, Shizuko Terasawa, Yuri Morisaki, Hiroshi Ogaki, Masao Baliki, Marwan N. |
author_sort | Wakaizumi, Kenta |
collection | PubMed |
description | Chronic pain (CP) is a global problem extensively associated with an unhealthy lifestyle. Time discounting (TD), a tendency to assign less value to future gains than to present gains, is an indicator of the unhealthy behaviors. While, recent neuroimaging studies implied overlapping neuro mechanisms underlying CP and TD, little is known about the specific relationship between CP and TD in behavior or neuroscience. As such, we investigated the association of TD with behavioral measures in CP and resting-state brain functional network in both CP patients and healthy subjects. Behaviorally, TD showed a significant correlation with meaningfulness in healthy subjects, whereas TD in patients only correlated with pain intensity. We identified a specific network including medial and dorsolateral prefrontal cortex (PFC) in default mode network (DMN) associated with TD in healthy subjects that showed significant indirect mediation effect of meaningfulness on TD. In contrast, TD in patients was correlated with functional connectivity between dorsolateral PFC (DLPFC) and temporal lobe that mediated the effect of pain intensity on TD in patients. These results imply that TD is modulated by pain intensity in CP patients, and the brain function associated to TD is shifted from a medial to lateral representation within the frontal regions. |
format | Online Article Text |
id | pubmed-6544657 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-65446572019-06-09 Altered functional connectivity associated with time discounting in chronic pain Wakaizumi, Kenta Jabakhanji, Rami Ihara, Naho Kosugi, Shizuko Terasawa, Yuri Morisaki, Hiroshi Ogaki, Masao Baliki, Marwan N. Sci Rep Article Chronic pain (CP) is a global problem extensively associated with an unhealthy lifestyle. Time discounting (TD), a tendency to assign less value to future gains than to present gains, is an indicator of the unhealthy behaviors. While, recent neuroimaging studies implied overlapping neuro mechanisms underlying CP and TD, little is known about the specific relationship between CP and TD in behavior or neuroscience. As such, we investigated the association of TD with behavioral measures in CP and resting-state brain functional network in both CP patients and healthy subjects. Behaviorally, TD showed a significant correlation with meaningfulness in healthy subjects, whereas TD in patients only correlated with pain intensity. We identified a specific network including medial and dorsolateral prefrontal cortex (PFC) in default mode network (DMN) associated with TD in healthy subjects that showed significant indirect mediation effect of meaningfulness on TD. In contrast, TD in patients was correlated with functional connectivity between dorsolateral PFC (DLPFC) and temporal lobe that mediated the effect of pain intensity on TD in patients. These results imply that TD is modulated by pain intensity in CP patients, and the brain function associated to TD is shifted from a medial to lateral representation within the frontal regions. Nature Publishing Group UK 2019-05-31 /pmc/articles/PMC6544657/ /pubmed/31148557 http://dx.doi.org/10.1038/s41598-019-44497-5 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Wakaizumi, Kenta Jabakhanji, Rami Ihara, Naho Kosugi, Shizuko Terasawa, Yuri Morisaki, Hiroshi Ogaki, Masao Baliki, Marwan N. Altered functional connectivity associated with time discounting in chronic pain |
title | Altered functional connectivity associated with time discounting in chronic pain |
title_full | Altered functional connectivity associated with time discounting in chronic pain |
title_fullStr | Altered functional connectivity associated with time discounting in chronic pain |
title_full_unstemmed | Altered functional connectivity associated with time discounting in chronic pain |
title_short | Altered functional connectivity associated with time discounting in chronic pain |
title_sort | altered functional connectivity associated with time discounting in chronic pain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544657/ https://www.ncbi.nlm.nih.gov/pubmed/31148557 http://dx.doi.org/10.1038/s41598-019-44497-5 |
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