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Identifying Dysfunctional Cortex: Dissociable Effects of Stroke and Aging on Resting State Dynamics in MEG and fMRI

Spontaneous signals in neuroimaging data may provide information on cortical health in disease and aging, but the relative sensitivity of different approaches is unknown. In the present study, we compared different but complementary indicators of neural dynamics in resting-state MEG and BOLD fMRI, a...

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Autores principales: Kielar, Aneta, Deschamps, Tiffany, Chu, Ron K. O., Jokel, Regina, Khatamian, Yasha B., Chen, Jean J., Meltzer, Jed A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776400/
https://www.ncbi.nlm.nih.gov/pubmed/26973515
http://dx.doi.org/10.3389/fnagi.2016.00040
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author Kielar, Aneta
Deschamps, Tiffany
Chu, Ron K. O.
Jokel, Regina
Khatamian, Yasha B.
Chen, Jean J.
Meltzer, Jed A.
author_facet Kielar, Aneta
Deschamps, Tiffany
Chu, Ron K. O.
Jokel, Regina
Khatamian, Yasha B.
Chen, Jean J.
Meltzer, Jed A.
author_sort Kielar, Aneta
collection PubMed
description Spontaneous signals in neuroimaging data may provide information on cortical health in disease and aging, but the relative sensitivity of different approaches is unknown. In the present study, we compared different but complementary indicators of neural dynamics in resting-state MEG and BOLD fMRI, and their relationship with blood flow. Participants included patients with post-stroke aphasia, age-matched controls, and young adults. The complexity of brain activity at rest was quantified in MEG using spectral analysis and multiscale entropy (MSE) measures, whereas BOLD variability was quantified as the standard deviation (SD(BOLD)), mean squared successive difference (MSSD), and sample entropy of the BOLD time series. We sought to assess the utility of signal variability and complexity measures as markers of age-related changes in healthy adults and perilesional dysfunction in chronic stroke. The results indicate that reduced BOLD variability is a robust finding in aging, whereas MEG measures are more sensitive to the cortical abnormalities associated with stroke. Furthermore, reduced complexity of MEG signals in perilesional tissue were correlated with hypoperfusion as assessed with arterial spin labeling (ASL), while no such relationship was apparent with BOLD variability. These findings suggest that MEG signal complexity offers a sensitive index of neural dysfunction in perilesional tissue in chronic stroke, and that these effects are clearly distinguishable from those associated with healthy aging.
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spelling pubmed-47764002016-03-11 Identifying Dysfunctional Cortex: Dissociable Effects of Stroke and Aging on Resting State Dynamics in MEG and fMRI Kielar, Aneta Deschamps, Tiffany Chu, Ron K. O. Jokel, Regina Khatamian, Yasha B. Chen, Jean J. Meltzer, Jed A. Front Aging Neurosci Neuroscience Spontaneous signals in neuroimaging data may provide information on cortical health in disease and aging, but the relative sensitivity of different approaches is unknown. In the present study, we compared different but complementary indicators of neural dynamics in resting-state MEG and BOLD fMRI, and their relationship with blood flow. Participants included patients with post-stroke aphasia, age-matched controls, and young adults. The complexity of brain activity at rest was quantified in MEG using spectral analysis and multiscale entropy (MSE) measures, whereas BOLD variability was quantified as the standard deviation (SD(BOLD)), mean squared successive difference (MSSD), and sample entropy of the BOLD time series. We sought to assess the utility of signal variability and complexity measures as markers of age-related changes in healthy adults and perilesional dysfunction in chronic stroke. The results indicate that reduced BOLD variability is a robust finding in aging, whereas MEG measures are more sensitive to the cortical abnormalities associated with stroke. Furthermore, reduced complexity of MEG signals in perilesional tissue were correlated with hypoperfusion as assessed with arterial spin labeling (ASL), while no such relationship was apparent with BOLD variability. These findings suggest that MEG signal complexity offers a sensitive index of neural dysfunction in perilesional tissue in chronic stroke, and that these effects are clearly distinguishable from those associated with healthy aging. Frontiers Media S.A. 2016-03-03 /pmc/articles/PMC4776400/ /pubmed/26973515 http://dx.doi.org/10.3389/fnagi.2016.00040 Text en Copyright © 2016 Kielar, Deschamps, Chu, Jokel, Khatamian, Chen and Meltzer. http://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) or licensor 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 Neuroscience
Kielar, Aneta
Deschamps, Tiffany
Chu, Ron K. O.
Jokel, Regina
Khatamian, Yasha B.
Chen, Jean J.
Meltzer, Jed A.
Identifying Dysfunctional Cortex: Dissociable Effects of Stroke and Aging on Resting State Dynamics in MEG and fMRI
title Identifying Dysfunctional Cortex: Dissociable Effects of Stroke and Aging on Resting State Dynamics in MEG and fMRI
title_full Identifying Dysfunctional Cortex: Dissociable Effects of Stroke and Aging on Resting State Dynamics in MEG and fMRI
title_fullStr Identifying Dysfunctional Cortex: Dissociable Effects of Stroke and Aging on Resting State Dynamics in MEG and fMRI
title_full_unstemmed Identifying Dysfunctional Cortex: Dissociable Effects of Stroke and Aging on Resting State Dynamics in MEG and fMRI
title_short Identifying Dysfunctional Cortex: Dissociable Effects of Stroke and Aging on Resting State Dynamics in MEG and fMRI
title_sort identifying dysfunctional cortex: dissociable effects of stroke and aging on resting state dynamics in meg and fmri
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776400/
https://www.ncbi.nlm.nih.gov/pubmed/26973515
http://dx.doi.org/10.3389/fnagi.2016.00040
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