Cortico-Brainstem Mechanisms of Biased Perceptual Decision-Making in the Context of Pain.


Journal

The journal of pain
ISSN: 1528-8447
Titre abrégé: J Pain
Pays: United States
ID NLM: 100898657

Informations de publication

Date de publication:
04 2022
Historique:
received: 03 06 2021
revised: 29 10 2021
accepted: 16 11 2021
pubmed: 3 12 2021
medline: 8 4 2022
entrez: 2 12 2021
Statut: ppublish

Résumé

Prior expectations can bias how we perceive pain. Using a drift diffusion model, we recently showed that this influence is primarily based on changes in perceptual decision-making (indexed as shift in starting point). Only during unexpected application of high-intensity noxious stimuli, altered information processing (indexed as increase in drift rate) explained the expectancy effect on pain processing. Here, we employed functional magnetic resonance imaging to investigate the neural basis of both these processes in healthy volunteers. On each trial, visual cues induced the expectation of high- or low-intensity noxious stimulation or signaled equal probability for both intensities. Participants categorized a subsequently applied electrical stimulus as either low- or high-intensity pain. A shift in starting point towards high pain correlated negatively with right dorsolateral prefrontal cortex activity during cue presentation underscoring its proposed role of "keeping pain out of mind". This anticipatory right dorsolateral prefrontal cortex signal increase was positively correlated with periaqueductal gray (PAG) activity when the expected high-intensity stimulation was applied. A drift rate increase during unexpected high-intensity pain was reflected in amygdala engagement and increased functional connectivity between amygdala and PAG. Our findings suggest involvement of the PAG in both decision-making bias and altered information processing to implement expectancy effects on pain. PERSPECTIVE: Modulation of pain through expectations has been linked to changes in perceptual decision-making and altered processing of afferent information. Our results suggest involvement of the dorsolateral prefrontal cortex, amygdala, and periaqueductal gray in these processes.

Identifiants

pubmed: 34856408
pii: S1526-5900(21)00371-0
doi: 10.1016/j.jpain.2021.11.006
pii:
doi:

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

680-692

Subventions

Organisme : Medical Research Council
ID : MR/L011719/1
Pays : United Kingdom

Informations de copyright

Copyright © 2022. Published by Elsevier Inc.

Auteurs

Katja Wiech (K)

Wellcome Centre for Integrative Neuroimaging (WIN), Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford, UK. Electronic address: katja.wiech@ndcn.ox.ac.uk.

Falk Eippert (F)

Wellcome Centre for Integrative Neuroimaging (WIN), Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford, UK; Max Planck Institute for Human Cognitive and Brain Sciences, Leipzig, Germany.

Joachim Vandekerckhove (J)

Department of Cognitive Sciences, University of California, Irvine, California; Research Group of Quantitative Psychology and Individual Differences, KU Leuven, Leuven, Belgium.

Jonas Zaman (J)

Research Group Health Psychology, KU Leuven, Leuven, Belgium.

Katerina Placek (K)

Takeda Pharmaceuticals, Statistics and Quantitative Sciences, Cambridge, Massachusetts.

Francis Tuerlinckx (F)

Research Group of Quantitative Psychology and Individual Differences, KU Leuven, Leuven, Belgium.

Johan W S Vlaeyen (JWS)

Research Group Health Psychology, KU Leuven, Leuven, Belgium; Research Group Experimental Health Psychology, Maastricht University, Maastricht, Netherlands.

Irene Tracey (I)

Wellcome Centre for Integrative Neuroimaging (WIN), Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, Oxford, UK.

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