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Resting-state MEG measurement of functional activation as a biomarker for cognitive decline in MS

BACKGROUND: Neurophysiological measures of brain function, such as magnetoencephalography (MEG), are widely used in clinical neurology and have strong relations with cognitive impairment and dementia but are still underdeveloped in multiple sclerosis (MS). OBJECTIVES: To demonstrate the value of cli...

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Autores principales: Schoonhoven, Deborah N, Fraschini, Matteo, Tewarie, Prejaas, Uitdehaag, Bernard MJ, Eijlers, Anand JC, Geurts, Jeroen JG, Hillebrand, Arjan, Schoonheim, Menno M, Stam, Cornelis J, Strijbis, Eva MM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875827/
https://www.ncbi.nlm.nih.gov/pubmed/30465461
http://dx.doi.org/10.1177/1352458518810260
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author Schoonhoven, Deborah N
Fraschini, Matteo
Tewarie, Prejaas
Uitdehaag, Bernard MJ
Eijlers, Anand JC
Geurts, Jeroen JG
Hillebrand, Arjan
Schoonheim, Menno M
Stam, Cornelis J
Strijbis, Eva MM
author_facet Schoonhoven, Deborah N
Fraschini, Matteo
Tewarie, Prejaas
Uitdehaag, Bernard MJ
Eijlers, Anand JC
Geurts, Jeroen JG
Hillebrand, Arjan
Schoonheim, Menno M
Stam, Cornelis J
Strijbis, Eva MM
author_sort Schoonhoven, Deborah N
collection PubMed
description BACKGROUND: Neurophysiological measures of brain function, such as magnetoencephalography (MEG), are widely used in clinical neurology and have strong relations with cognitive impairment and dementia but are still underdeveloped in multiple sclerosis (MS). OBJECTIVES: To demonstrate the value of clinically applicable MEG-measures in evaluating cognitive impairment in MS. METHODS: In eyes-closed resting-state, MEG data of 83 MS patients and 34 healthy controls (HCs) peak frequencies and relative power of six canonical frequency bands for 78 cortical and 10 deep gray matter (DGM) areas were calculated. Linear regression models, correcting for age, gender, and education, assessed the relation between cognitive performance and MEG biomarkers. RESULTS: Increased alpha1 and theta power was strongly associated with impaired cognition in patients, which differed between cognitively impaired (CI) patients and HCs in bilateral parietotemporal cortices. CI patients had a lower peak frequency than HCs. Oscillatory slowing was also widespread in the DGM, most pronounced in the thalamus. CONCLUSION: There is a clinically relevant slowing of neuronal activity in MS patients in parietotemporal cortical areas and the thalamus, strongly related to cognitive impairment. These measures hold promise for the application of resting-state MEG as a biomarker for cognitive disturbances in MS in a clinical setting.
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spelling pubmed-68758272019-12-24 Resting-state MEG measurement of functional activation as a biomarker for cognitive decline in MS Schoonhoven, Deborah N Fraschini, Matteo Tewarie, Prejaas Uitdehaag, Bernard MJ Eijlers, Anand JC Geurts, Jeroen JG Hillebrand, Arjan Schoonheim, Menno M Stam, Cornelis J Strijbis, Eva MM Mult Scler Original Research Papers BACKGROUND: Neurophysiological measures of brain function, such as magnetoencephalography (MEG), are widely used in clinical neurology and have strong relations with cognitive impairment and dementia but are still underdeveloped in multiple sclerosis (MS). OBJECTIVES: To demonstrate the value of clinically applicable MEG-measures in evaluating cognitive impairment in MS. METHODS: In eyes-closed resting-state, MEG data of 83 MS patients and 34 healthy controls (HCs) peak frequencies and relative power of six canonical frequency bands for 78 cortical and 10 deep gray matter (DGM) areas were calculated. Linear regression models, correcting for age, gender, and education, assessed the relation between cognitive performance and MEG biomarkers. RESULTS: Increased alpha1 and theta power was strongly associated with impaired cognition in patients, which differed between cognitively impaired (CI) patients and HCs in bilateral parietotemporal cortices. CI patients had a lower peak frequency than HCs. Oscillatory slowing was also widespread in the DGM, most pronounced in the thalamus. CONCLUSION: There is a clinically relevant slowing of neuronal activity in MS patients in parietotemporal cortical areas and the thalamus, strongly related to cognitive impairment. These measures hold promise for the application of resting-state MEG as a biomarker for cognitive disturbances in MS in a clinical setting. SAGE Publications 2018-11-22 2019-12 /pmc/articles/PMC6875827/ /pubmed/30465461 http://dx.doi.org/10.1177/1352458518810260 Text en © The Author(s), 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Papers
Schoonhoven, Deborah N
Fraschini, Matteo
Tewarie, Prejaas
Uitdehaag, Bernard MJ
Eijlers, Anand JC
Geurts, Jeroen JG
Hillebrand, Arjan
Schoonheim, Menno M
Stam, Cornelis J
Strijbis, Eva MM
Resting-state MEG measurement of functional activation as a biomarker for cognitive decline in MS
title Resting-state MEG measurement of functional activation as a biomarker for cognitive decline in MS
title_full Resting-state MEG measurement of functional activation as a biomarker for cognitive decline in MS
title_fullStr Resting-state MEG measurement of functional activation as a biomarker for cognitive decline in MS
title_full_unstemmed Resting-state MEG measurement of functional activation as a biomarker for cognitive decline in MS
title_short Resting-state MEG measurement of functional activation as a biomarker for cognitive decline in MS
title_sort resting-state meg measurement of functional activation as a biomarker for cognitive decline in ms
topic Original Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6875827/
https://www.ncbi.nlm.nih.gov/pubmed/30465461
http://dx.doi.org/10.1177/1352458518810260
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