Temporal structure of brain oscillations predicts learned nocebo responses to pain

Abstract 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...

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Main Authors: Mia A. Thomaidou, Joseph S. Blythe, Simon J. Houtman, Dieuwke S. Veldhuijzen, Antoinette I. M. van Laarhoven, Andrea W. M. Evers
Format: Article
Language:English
Published: Nature Publishing Group 2021-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-89368-0
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spelling doaj-a3345848cb3643cf9a36cc3d74422efd2021-05-09T11:34:38ZengNature Publishing GroupScientific Reports2045-23222021-05-0111111210.1038/s41598-021-89368-0Temporal structure of brain oscillations predicts learned nocebo responses to painMia A. Thomaidou0Joseph S. Blythe1Simon J. Houtman2Dieuwke S. Veldhuijzen3Antoinette I. M. van Laarhoven4Andrea W. M. Evers5Faculty of Social and Behavioral Sciences, Leiden UniversityFaculty of Social and Behavioral Sciences, Leiden UniversityDepartment of Integrative Neurophysiology, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, VU University AmsterdamFaculty of Social and Behavioral Sciences, Leiden UniversityFaculty of Social and Behavioral Sciences, Leiden UniversityFaculty of Social and Behavioral Sciences, Leiden UniversityAbstract 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.https://doi.org/10.1038/s41598-021-89368-0
collection DOAJ
language English
format Article
sources DOAJ
author Mia A. Thomaidou
Joseph S. Blythe
Simon J. Houtman
Dieuwke S. Veldhuijzen
Antoinette I. M. van Laarhoven
Andrea W. M. Evers
spellingShingle Mia A. Thomaidou
Joseph S. Blythe
Simon J. Houtman
Dieuwke S. Veldhuijzen
Antoinette I. M. van Laarhoven
Andrea W. M. Evers
Temporal structure of brain oscillations predicts learned nocebo responses to pain
Scientific Reports
author_facet Mia A. Thomaidou
Joseph S. Blythe
Simon J. Houtman
Dieuwke S. Veldhuijzen
Antoinette I. M. van Laarhoven
Andrea W. M. Evers
author_sort Mia A. Thomaidou
title 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_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_sort temporal structure of brain oscillations predicts learned nocebo responses to pain
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-05-01
description Abstract 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.
url https://doi.org/10.1038/s41598-021-89368-0
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