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Characterization of cortical source generators based on electroencephalography during tonic pain
OBJECTIVE: The aim of the present study was to characterize the cortical source generators evoked by experimental tonic pain. METHODS: Electroencephalography (EEG) was recorded on two separate days during rest and with immersion of the hand in ice water for 2 minutes (cold pressor test). Exact low-r...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476635/ https://www.ncbi.nlm.nih.gov/pubmed/28652806 http://dx.doi.org/10.2147/JPR.S132909 |
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author | Hansen, Tine Maria Mark, Esben Bolvig Olesen, Søren Schou Gram, Mikkel Frøkjær, Jens Brøndum Drewes, Asbjørn Mohr |
author_facet | Hansen, Tine Maria Mark, Esben Bolvig Olesen, Søren Schou Gram, Mikkel Frøkjær, Jens Brøndum Drewes, Asbjørn Mohr |
author_sort | Hansen, Tine Maria |
collection | PubMed |
description | OBJECTIVE: The aim of the present study was to characterize the cortical source generators evoked by experimental tonic pain. METHODS: Electroencephalography (EEG) was recorded on two separate days during rest and with immersion of the hand in ice water for 2 minutes (cold pressor test). Exact low-resolution brain electromagnetic tomography source localization was performed in 31 healthy volunteers to characterize the cortical source generators. RESULTS: Reliability was high in all eight frequency bands during rest and cold pressor conditions (intraclass coefficients =0.47–0.83 in the cingulate and insula). Tonic pain increased cortical activities in the delta (1–4 Hz), theta (4–8 Hz), beta1 (12–18 Hz), beta2 (18–24 Hz), beta3 (24–32 Hz), and gamma (32–60 Hz) bands (all P<0.011) in widespread areas mainly in the limbic system, whereas decreased cortical activities were found in cingulate and pre- and postcentral gyri in the alpha2 (10–12 Hz) band (P=0.007). The pain intensity was correlated with cingulate activity in the beta2, beta3, and gamma bands (all P<0.04). CONCLUSION: Source localization of EEG is a reliable method to estimate cortical source generators. Activities in different brain regions, mainly in the limbic system, showed fluctuations in various frequency bands. Cingulate changes were correlated with pain intensity. SIGNIFICANCE: This method might add information to the objective assessment of the cortical pain response in future experimental pain studies. |
format | Online Article Text |
id | pubmed-5476635 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54766352017-06-26 Characterization of cortical source generators based on electroencephalography during tonic pain Hansen, Tine Maria Mark, Esben Bolvig Olesen, Søren Schou Gram, Mikkel Frøkjær, Jens Brøndum Drewes, Asbjørn Mohr J Pain Res Original Research OBJECTIVE: The aim of the present study was to characterize the cortical source generators evoked by experimental tonic pain. METHODS: Electroencephalography (EEG) was recorded on two separate days during rest and with immersion of the hand in ice water for 2 minutes (cold pressor test). Exact low-resolution brain electromagnetic tomography source localization was performed in 31 healthy volunteers to characterize the cortical source generators. RESULTS: Reliability was high in all eight frequency bands during rest and cold pressor conditions (intraclass coefficients =0.47–0.83 in the cingulate and insula). Tonic pain increased cortical activities in the delta (1–4 Hz), theta (4–8 Hz), beta1 (12–18 Hz), beta2 (18–24 Hz), beta3 (24–32 Hz), and gamma (32–60 Hz) bands (all P<0.011) in widespread areas mainly in the limbic system, whereas decreased cortical activities were found in cingulate and pre- and postcentral gyri in the alpha2 (10–12 Hz) band (P=0.007). The pain intensity was correlated with cingulate activity in the beta2, beta3, and gamma bands (all P<0.04). CONCLUSION: Source localization of EEG is a reliable method to estimate cortical source generators. Activities in different brain regions, mainly in the limbic system, showed fluctuations in various frequency bands. Cingulate changes were correlated with pain intensity. SIGNIFICANCE: This method might add information to the objective assessment of the cortical pain response in future experimental pain studies. Dove Medical Press 2017-06-07 /pmc/articles/PMC5476635/ /pubmed/28652806 http://dx.doi.org/10.2147/JPR.S132909 Text en © 2017 Hansen et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Hansen, Tine Maria Mark, Esben Bolvig Olesen, Søren Schou Gram, Mikkel Frøkjær, Jens Brøndum Drewes, Asbjørn Mohr Characterization of cortical source generators based on electroencephalography during tonic pain |
title | Characterization of cortical source generators based on electroencephalography during tonic pain |
title_full | Characterization of cortical source generators based on electroencephalography during tonic pain |
title_fullStr | Characterization of cortical source generators based on electroencephalography during tonic pain |
title_full_unstemmed | Characterization of cortical source generators based on electroencephalography during tonic pain |
title_short | Characterization of cortical source generators based on electroencephalography during tonic pain |
title_sort | characterization of cortical source generators based on electroencephalography during tonic pain |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5476635/ https://www.ncbi.nlm.nih.gov/pubmed/28652806 http://dx.doi.org/10.2147/JPR.S132909 |
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