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Altered physiological brain variation in drug‐resistant epilepsy
INTRODUCTION: Functional magnetic resonance imaging (fMRI) combined with simultaneous electroencephalography (EEG‐fMRI) has become a major tool in mapping epilepsy sources. In the absence of detectable epileptiform activity, the resting state fMRI may still detect changes in the blood oxygen level‐d...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160661/ https://www.ncbi.nlm.nih.gov/pubmed/30112813 http://dx.doi.org/10.1002/brb3.1090 |
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author | Kananen, Janne Tuovinen, Timo Ansakorpi, Hanna Rytky, Seppo Helakari, Heta Huotari, Niko Raitamaa, Lauri Raatikainen, Ville Rasila, Aleksi Borchardt, Viola Korhonen, Vesa LeVan, Pierre Nedergaard, Maiken Kiviniemi, Vesa |
author_facet | Kananen, Janne Tuovinen, Timo Ansakorpi, Hanna Rytky, Seppo Helakari, Heta Huotari, Niko Raitamaa, Lauri Raatikainen, Ville Rasila, Aleksi Borchardt, Viola Korhonen, Vesa LeVan, Pierre Nedergaard, Maiken Kiviniemi, Vesa |
author_sort | Kananen, Janne |
collection | PubMed |
description | INTRODUCTION: Functional magnetic resonance imaging (fMRI) combined with simultaneous electroencephalography (EEG‐fMRI) has become a major tool in mapping epilepsy sources. In the absence of detectable epileptiform activity, the resting state fMRI may still detect changes in the blood oxygen level‐dependent signal, suggesting intrinsic alterations in the underlying brain physiology. METHODS: In this study, we used coefficient of variation (CV) of critically sampled 10 Hz ultra‐fast fMRI (magnetoencephalography, MREG) signal to compare physiological variance between healthy controls (n = 10) and patients (n = 10) with drug‐resistant epilepsy (DRE). RESULTS: We showed highly significant voxel‐level (p < 0.01, TFCE‐corrected) increase in the physiological variance in DRE patients. At individual level, the elevations range over three standard deviations (σ) above the control mean (μ) CV(MREG) values solely in DRE patients, enabling patient‐specific mapping of elevated physiological variance. The most apparent differences in group‐level analysis are found on white matter, brainstem, and cerebellum. Respiratory (0.12–0.4 Hz) and very‐low‐frequency (VLF = 0.009–0.1 Hz) signal variances were most affected. CONCLUSIONS: The CV(MREG) increase was not explained by head motion or physiological cardiorespiratory activity, that is, it seems to be linked to intrinsic physiological pulsations. We suggest that intrinsic brain pulsations play a role in DRE and that critically sampled fMRI may provide a powerful tool for their identification. |
format | Online Article Text |
id | pubmed-6160661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61606612018-10-01 Altered physiological brain variation in drug‐resistant epilepsy Kananen, Janne Tuovinen, Timo Ansakorpi, Hanna Rytky, Seppo Helakari, Heta Huotari, Niko Raitamaa, Lauri Raatikainen, Ville Rasila, Aleksi Borchardt, Viola Korhonen, Vesa LeVan, Pierre Nedergaard, Maiken Kiviniemi, Vesa Brain Behav Original Research INTRODUCTION: Functional magnetic resonance imaging (fMRI) combined with simultaneous electroencephalography (EEG‐fMRI) has become a major tool in mapping epilepsy sources. In the absence of detectable epileptiform activity, the resting state fMRI may still detect changes in the blood oxygen level‐dependent signal, suggesting intrinsic alterations in the underlying brain physiology. METHODS: In this study, we used coefficient of variation (CV) of critically sampled 10 Hz ultra‐fast fMRI (magnetoencephalography, MREG) signal to compare physiological variance between healthy controls (n = 10) and patients (n = 10) with drug‐resistant epilepsy (DRE). RESULTS: We showed highly significant voxel‐level (p < 0.01, TFCE‐corrected) increase in the physiological variance in DRE patients. At individual level, the elevations range over three standard deviations (σ) above the control mean (μ) CV(MREG) values solely in DRE patients, enabling patient‐specific mapping of elevated physiological variance. The most apparent differences in group‐level analysis are found on white matter, brainstem, and cerebellum. Respiratory (0.12–0.4 Hz) and very‐low‐frequency (VLF = 0.009–0.1 Hz) signal variances were most affected. CONCLUSIONS: The CV(MREG) increase was not explained by head motion or physiological cardiorespiratory activity, that is, it seems to be linked to intrinsic physiological pulsations. We suggest that intrinsic brain pulsations play a role in DRE and that critically sampled fMRI may provide a powerful tool for their identification. John Wiley and Sons Inc. 2018-08-15 /pmc/articles/PMC6160661/ /pubmed/30112813 http://dx.doi.org/10.1002/brb3.1090 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Kananen, Janne Tuovinen, Timo Ansakorpi, Hanna Rytky, Seppo Helakari, Heta Huotari, Niko Raitamaa, Lauri Raatikainen, Ville Rasila, Aleksi Borchardt, Viola Korhonen, Vesa LeVan, Pierre Nedergaard, Maiken Kiviniemi, Vesa Altered physiological brain variation in drug‐resistant epilepsy |
title | Altered physiological brain variation in drug‐resistant epilepsy |
title_full | Altered physiological brain variation in drug‐resistant epilepsy |
title_fullStr | Altered physiological brain variation in drug‐resistant epilepsy |
title_full_unstemmed | Altered physiological brain variation in drug‐resistant epilepsy |
title_short | Altered physiological brain variation in drug‐resistant epilepsy |
title_sort | altered physiological brain variation in drug‐resistant epilepsy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6160661/ https://www.ncbi.nlm.nih.gov/pubmed/30112813 http://dx.doi.org/10.1002/brb3.1090 |
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