ArticleJournal of cognitive neuroscience2014
EEG frequency tagging to dissociate the cortical responses to nociceptive and nonnociceptive stimuli.
Article in Journal of cognitive neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 18 citations in OpenAlex.
- Dynamics of the perception and EEG signals triggered by tonic warm and cool stimulation.PloS one · 2020Trial
- The role of competing grouping patterns and tonal coherence in neural synchronization to musical meter.Experimental brain research · 2025Article
- Cue-based modulation of pain stimulus expectation: do ongoing oscillations reflect changes in pain perception? A registered report.Royal Society open science · 2024Article
- Processing the fine-grained features of tactile textures involves the primary somatosensory cortex.Imaging neuroscience (Cambridge, Mass.) · 2024Article
- Bayesian analysis of phase data in EEG and MEG.eLife · 2023Article
- Excitatory versus inhibitory feedback in Bayesian formulations of scene construction.Journal of the Royal Society, Interface · 2019Article
- EEG frequency tagging using ultra-slow periodic heat stimulation of the skin reveals cortical activity specifically related to C fiber thermonociceptors.NeuroImage · 2017Article
- Absence of Evidence or Evidence of Absence? Commentary: Captured by the pain: Pain steady-state evoked potentials are not modulated by selective spatial attention.Frontiers in human neuroscience · 2016Article
Corrections and comments
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
Abstract
Whether the cortical processing of nociceptive input relies on the activity of nociceptive-specific neurons or whether it relies on the activity of neurons also involved in processing nonnociceptive sensory input remains a matter of debate. Here, we combined EEG "frequency tagging" of steady-state evoked potentials (SS-EPs) with an intermodal selective attention paradigm to test whether the cortical processing of nociceptive input relies on nociceptive-specific neuronal populations that can be selectively modulated by top-down attention. Trains of nociceptive and vibrotactile stimuli (Experiment 1) and trains of nociceptive and visual stimuli (Experiment 2) were applied concomitantly to the same hand, thus eliciting nociceptive, vibrotactile, and visual SS-EPs. In each experiment, a target detection task was used to focus attention toward one of the two concurrent streams of sensory input. We found that selectively attending to nociceptive or vibrotactile somatosensory input indistinctly enhances the magnitude of nociceptive and vibrotactile SS-EPs, whereas selectively attending to nociceptive or visual input independently enhances the magnitude of the SS-EP elicited by the attended sensory input. This differential effect indicates that the processing of nociceptive input involves neuronal populations also involved in the processing of touch, but distinct from the neuronal populations involved in vision.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.