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PainVision-based evaluation of brain potentials: a novel approach for quantitative pain assessment
Introduction: The complex and multidimensional nature of pain poses a major challenge in clinical pain assessments. In this study, we aimed to evaluate a novel approach combining quantitative sensory testing (QST) with event-related potential measurements for assessment of experimental pain in healt...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338958/ https://www.ncbi.nlm.nih.gov/pubmed/37456719 http://dx.doi.org/10.3389/fbioe.2023.1197070 |
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author | Chen, Li Zhang, Zhen Han, Rui Du, Liyuan Li, Zhenxing Liu, Shuiping Huang, Dong Zhou, Haocheng |
author_facet | Chen, Li Zhang, Zhen Han, Rui Du, Liyuan Li, Zhenxing Liu, Shuiping Huang, Dong Zhou, Haocheng |
author_sort | Chen, Li |
collection | PubMed |
description | Introduction: The complex and multidimensional nature of pain poses a major challenge in clinical pain assessments. In this study, we aimed to evaluate a novel approach combining quantitative sensory testing (QST) with event-related potential measurements for assessment of experimental pain in healthy individuals. Methods: QST was performed with a commercial device (PainVision, PS-2100), and numeric rating scale (NRS) scores after exposure to different sensory stimuli were reported by the participants. Resting-state electroencephalography (EEG) was simultaneously performed to capture the cortical responses to peripheral stimulation. Results: Pain scores increased with the intensity of stimuli, with mean NRS scores of 2.7 ± 1.0 after mild stimuli and 5.6 ± 1.0 after moderate stimuli. A reproducible, significant P2-N2 complex was evoked by both mild and moderately painful stimuli, but not by non-painful stimuli. The latency of pain-related potentials was not significantly different between stimuli. The amplitudes of both P2 and N2 components significantly increased when intense nociception was applied, and the increments mainly originated from theta oscillations. Conclusion: The combination of QST with EEG was feasible for subjective and objective pain assessment. Distinct patterns of brain potentials were associated with the phenotype of the peripheral stimuli (e.g., noxious versus. innoxious, high versus. low pain intensity). |
format | Online Article Text |
id | pubmed-10338958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103389582023-07-14 PainVision-based evaluation of brain potentials: a novel approach for quantitative pain assessment Chen, Li Zhang, Zhen Han, Rui Du, Liyuan Li, Zhenxing Liu, Shuiping Huang, Dong Zhou, Haocheng Front Bioeng Biotechnol Bioengineering and Biotechnology Introduction: The complex and multidimensional nature of pain poses a major challenge in clinical pain assessments. In this study, we aimed to evaluate a novel approach combining quantitative sensory testing (QST) with event-related potential measurements for assessment of experimental pain in healthy individuals. Methods: QST was performed with a commercial device (PainVision, PS-2100), and numeric rating scale (NRS) scores after exposure to different sensory stimuli were reported by the participants. Resting-state electroencephalography (EEG) was simultaneously performed to capture the cortical responses to peripheral stimulation. Results: Pain scores increased with the intensity of stimuli, with mean NRS scores of 2.7 ± 1.0 after mild stimuli and 5.6 ± 1.0 after moderate stimuli. A reproducible, significant P2-N2 complex was evoked by both mild and moderately painful stimuli, but not by non-painful stimuli. The latency of pain-related potentials was not significantly different between stimuli. The amplitudes of both P2 and N2 components significantly increased when intense nociception was applied, and the increments mainly originated from theta oscillations. Conclusion: The combination of QST with EEG was feasible for subjective and objective pain assessment. Distinct patterns of brain potentials were associated with the phenotype of the peripheral stimuli (e.g., noxious versus. innoxious, high versus. low pain intensity). Frontiers Media S.A. 2023-06-29 /pmc/articles/PMC10338958/ /pubmed/37456719 http://dx.doi.org/10.3389/fbioe.2023.1197070 Text en Copyright © 2023 Chen, Zhang, Han, Du, Li, Liu, Huang and Zhou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Chen, Li Zhang, Zhen Han, Rui Du, Liyuan Li, Zhenxing Liu, Shuiping Huang, Dong Zhou, Haocheng PainVision-based evaluation of brain potentials: a novel approach for quantitative pain assessment |
title | PainVision-based evaluation of brain potentials: a novel approach for quantitative pain assessment |
title_full | PainVision-based evaluation of brain potentials: a novel approach for quantitative pain assessment |
title_fullStr | PainVision-based evaluation of brain potentials: a novel approach for quantitative pain assessment |
title_full_unstemmed | PainVision-based evaluation of brain potentials: a novel approach for quantitative pain assessment |
title_short | PainVision-based evaluation of brain potentials: a novel approach for quantitative pain assessment |
title_sort | painvision-based evaluation of brain potentials: a novel approach for quantitative pain assessment |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10338958/ https://www.ncbi.nlm.nih.gov/pubmed/37456719 http://dx.doi.org/10.3389/fbioe.2023.1197070 |
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