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Temporal structure of brain oscillations predicts learned nocebo responses to pain
This study aimed to identify electrophysiological correlates of nocebo-augmented pain. Nocebo hyperalgesia (i.e., increases in perceived pain resulting from negative expectations) has been found to impact how healthy and patient populations experience pain and is a phenomenon that could be better un...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8105329/ https://www.ncbi.nlm.nih.gov/pubmed/33963251 http://dx.doi.org/10.1038/s41598-021-89368-0 |
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author | Thomaidou, Mia A. Blythe, Joseph S. Houtman, Simon J. Veldhuijzen, Dieuwke S. van Laarhoven, Antoinette I. M. Evers, Andrea W. M. |
author_facet | Thomaidou, Mia A. Blythe, Joseph S. Houtman, Simon J. Veldhuijzen, Dieuwke S. van Laarhoven, Antoinette I. M. Evers, Andrea W. M. |
author_sort | Thomaidou, Mia A. |
collection | PubMed |
description | This study aimed to identify electrophysiological correlates of nocebo-augmented pain. Nocebo hyperalgesia (i.e., increases in perceived pain resulting from negative expectations) has been found to impact how healthy and patient populations experience pain and is a phenomenon that could be better understood in terms of its neurophysiological underpinnings. In this study, nocebo hyperalgesia was induced in 36 healthy participants through classical conditioning and negative suggestions. Electroencephalography was recorded during rest (pre- and post-acquisition) and during pain stimulation (baseline, acquisition, evocation) First, participants received baseline high thermal pain stimulations. During nocebo acquisition, participants learned to associate an inert gel applied to their forearm with administered high pain stimuli, relative to moderate intensity control stimuli administered without gel. During evocation, all stimuli were accompanied by moderate pain, to measure nocebo responses to the inert gel. Pre- to post-acquisition beta-band alterations in long-range temporal correlations (LRTC) were negatively associated with nocebo magnitudes. Individuals with strong resting LRTC showed larger nocebo responses than those with weaker LRTC. Nocebo acquisition trials showed reduced alpha power. Alpha power was higher while LRTC were lower during nocebo-augmented pain, compared to baseline. These findings support nocebo learning theories and highlight a role of nocebo-induced cognitive processing. |
format | Online Article Text |
id | pubmed-8105329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81053292021-05-10 Temporal structure of brain oscillations predicts learned nocebo responses to pain Thomaidou, Mia A. Blythe, Joseph S. Houtman, Simon J. Veldhuijzen, Dieuwke S. van Laarhoven, Antoinette I. M. Evers, Andrea W. M. Sci Rep Article This study aimed to identify electrophysiological correlates of nocebo-augmented pain. Nocebo hyperalgesia (i.e., increases in perceived pain resulting from negative expectations) has been found to impact how healthy and patient populations experience pain and is a phenomenon that could be better understood in terms of its neurophysiological underpinnings. In this study, nocebo hyperalgesia was induced in 36 healthy participants through classical conditioning and negative suggestions. Electroencephalography was recorded during rest (pre- and post-acquisition) and during pain stimulation (baseline, acquisition, evocation) First, participants received baseline high thermal pain stimulations. During nocebo acquisition, participants learned to associate an inert gel applied to their forearm with administered high pain stimuli, relative to moderate intensity control stimuli administered without gel. During evocation, all stimuli were accompanied by moderate pain, to measure nocebo responses to the inert gel. Pre- to post-acquisition beta-band alterations in long-range temporal correlations (LRTC) were negatively associated with nocebo magnitudes. Individuals with strong resting LRTC showed larger nocebo responses than those with weaker LRTC. Nocebo acquisition trials showed reduced alpha power. Alpha power was higher while LRTC were lower during nocebo-augmented pain, compared to baseline. These findings support nocebo learning theories and highlight a role of nocebo-induced cognitive processing. Nature Publishing Group UK 2021-05-07 /pmc/articles/PMC8105329/ /pubmed/33963251 http://dx.doi.org/10.1038/s41598-021-89368-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Thomaidou, Mia A. Blythe, Joseph S. Houtman, Simon J. Veldhuijzen, Dieuwke S. van Laarhoven, Antoinette I. M. Evers, Andrea W. M. Temporal structure of brain oscillations predicts learned nocebo responses to pain |
title | Temporal structure of brain oscillations predicts learned nocebo responses to pain |
title_full | Temporal structure of brain oscillations predicts learned nocebo responses to pain |
title_fullStr | Temporal structure of brain oscillations predicts learned nocebo responses to pain |
title_full_unstemmed | Temporal structure of brain oscillations predicts learned nocebo responses to pain |
title_short | Temporal structure of brain oscillations predicts learned nocebo responses to pain |
title_sort | temporal structure of brain oscillations predicts learned nocebo responses to pain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8105329/ https://www.ncbi.nlm.nih.gov/pubmed/33963251 http://dx.doi.org/10.1038/s41598-021-89368-0 |
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