ArticleHuman brain mapping2017
Evidence-based source modeling of nociceptive cortical responses: A direct comparison of scalp and intracranial activity in humans.
Article in Human brain mapping, 2017. 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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8 citing papers in PubMed.
- Normative data of laser evoked potentials using Nd:YAP laser.Clinical neurophysiology practice · 2026Article
- Cue-based modulation of pain stimulus expectation: do ongoing oscillations reflect changes in pain perception? A registered report.Royal Society open science · 2024Article
- Local brain oscillations and interregional connectivity differentially serve sensory and expectation effects on pain.Science advances · 2023Article
- Intracortical Functional Connectivity Predicts Arousal to Noxious Stimuli during Sleep in Humans.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021Article
- Neural oscillations and connectivity characterizing the state of tonic experimental pain in humans.Human brain mapping · 2020Article
- Distinct patterns of brain activity mediate perceptual and motor and autonomic responses to noxious stimuli.Nature communications · 2018Article
- Convergence of sensory and limbic noxious input into the anterior insula and the emergence of pain from nociception.Scientific reports · 2018Article
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3 authors.
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Abstract
backgroundSource modeling of EEG traditionally relies on interplay between physiological hypotheses and mathematical estimates. We propose to optimize the process by using evidence gathered from brain imaging and intracortical recordings.
methodsWe recorded laser-evoked potentials in 18 healthy participants, using high-density EEG. Brain sources were modeled during the first second poststimulus, constraining their initial position to regions where nociceptive-related activity has been ascertained by intracranial EEG. These comprised the two posterior operculo-insular regions, primary sensorimotor, posterior parietal, anterior cingulate/supplementary motor (ACC/SMA), bilateral frontal/anterior insular, and posterior cingulate (PCC) cortices.
resultsThe model yielded an average goodness of fit of 91% for individual and 95.8% for grand-average data. When compared with intracranial recordings from 27 human subjects, no significant difference in peak latencies was observed between modeled and intracranial data for 5 of the 6 assessable regions. Morphological match was excellent for operculo-insular, frontal, ACC/SMA and PCC regions (cross-correlation > 0.7) and fair for sensori-motor and posterior parietal cortex (c-c ∼ 0.5).
conclusionsMultiple overlapping activities evoked by nociceptive input can be disentangled from high-density scalp EEG guided by intracranial data. Modeled sources accurately described the timing and morphology of most activities recorded with intracranial electrodes, including those coinciding with the emergence of stimulus awareness. Hum Brain Mapp 38:6083-6095, 2017. © 2017 Wiley Periodicals, Inc.
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