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EEG spectral exponent as a synthetic index for the longitudinal assessment of stroke recovery

OBJECTIVE: Quantitative Electroencephalography (qEEG) can capture changes in brain activity following stroke. qEEG metrics traditionally focus on oscillatory activity, however recent findings highlight the importance of aperiodic (power-law) structure in characterizing pathological brain states. We...

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Autores principales: Lanzone, J., Colombo, M.A., Sarasso, S., Zappasodi, F., Rosanova, M., Massimini, M., Di Lazzaro, V., Assenza, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038588/
https://www.ncbi.nlm.nih.gov/pubmed/35303540
http://dx.doi.org/10.1016/j.clinph.2022.02.022
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author Lanzone, J.
Colombo, M.A.
Sarasso, S.
Zappasodi, F.
Rosanova, M.
Massimini, M.
Di Lazzaro, V.
Assenza, G.
author_facet Lanzone, J.
Colombo, M.A.
Sarasso, S.
Zappasodi, F.
Rosanova, M.
Massimini, M.
Di Lazzaro, V.
Assenza, G.
author_sort Lanzone, J.
collection PubMed
description OBJECTIVE: Quantitative Electroencephalography (qEEG) can capture changes in brain activity following stroke. qEEG metrics traditionally focus on oscillatory activity, however recent findings highlight the importance of aperiodic (power-law) structure in characterizing pathological brain states. We assessed neurophysiological alterations and recovery after mono-hemispheric stroke by means of the Spectral Exponent (SE), a metric that reflects EEG slowing and quantifies the power-law decay of the EEG Power Spectral Density (PSD). METHODS: Eighteen patients (n = 18) with mild to moderate mono-hemispheric Middle Cerebral Artery (MCA) ischaemic stroke were retrospectively enrolled for this study. Patients underwent EEG recording in the sub-acute phase (T0) and after 2 months of physical rehabilitation (T1). Sixteen healthy controls (HC; n = 16) matched by age and sex were enrolled as a normative group. SE values and narrow-band PSD were estimated for each recording. We compared SE and band-power between patients and HC, and between the affected (AH) and unaffected hemisphere (UH) at T0 and T1 in patients. RESULTS: At T0, stroke patients showed significantly more negative SE values than HC (p = 0.003), reflecting broad-band EEG slowing. Most important, in patients SE over the AH was consistently more negative compared to the UH and showed a renormalization at T1. This SE renormalization significantly correlated with National Institute of Health Stroke Scale (NIHSS) improvement (R = 0.63, p = 0.005). CONCLUSIONS: SE is a reliable readout of the neurophysiological and clinical alterations occurring after an ischaemic cortical lesion. SIGNIFICANCE: SE promise to be a robust method to monitor and predict patients’ functional outcome.
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spelling pubmed-90385882022-05-24 EEG spectral exponent as a synthetic index for the longitudinal assessment of stroke recovery Lanzone, J. Colombo, M.A. Sarasso, S. Zappasodi, F. Rosanova, M. Massimini, M. Di Lazzaro, V. Assenza, G. Clin Neurophysiol Article OBJECTIVE: Quantitative Electroencephalography (qEEG) can capture changes in brain activity following stroke. qEEG metrics traditionally focus on oscillatory activity, however recent findings highlight the importance of aperiodic (power-law) structure in characterizing pathological brain states. We assessed neurophysiological alterations and recovery after mono-hemispheric stroke by means of the Spectral Exponent (SE), a metric that reflects EEG slowing and quantifies the power-law decay of the EEG Power Spectral Density (PSD). METHODS: Eighteen patients (n = 18) with mild to moderate mono-hemispheric Middle Cerebral Artery (MCA) ischaemic stroke were retrospectively enrolled for this study. Patients underwent EEG recording in the sub-acute phase (T0) and after 2 months of physical rehabilitation (T1). Sixteen healthy controls (HC; n = 16) matched by age and sex were enrolled as a normative group. SE values and narrow-band PSD were estimated for each recording. We compared SE and band-power between patients and HC, and between the affected (AH) and unaffected hemisphere (UH) at T0 and T1 in patients. RESULTS: At T0, stroke patients showed significantly more negative SE values than HC (p = 0.003), reflecting broad-band EEG slowing. Most important, in patients SE over the AH was consistently more negative compared to the UH and showed a renormalization at T1. This SE renormalization significantly correlated with National Institute of Health Stroke Scale (NIHSS) improvement (R = 0.63, p = 0.005). CONCLUSIONS: SE is a reliable readout of the neurophysiological and clinical alterations occurring after an ischaemic cortical lesion. SIGNIFICANCE: SE promise to be a robust method to monitor and predict patients’ functional outcome. Elsevier 2022-05 /pmc/articles/PMC9038588/ /pubmed/35303540 http://dx.doi.org/10.1016/j.clinph.2022.02.022 Text en © 2022 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lanzone, J.
Colombo, M.A.
Sarasso, S.
Zappasodi, F.
Rosanova, M.
Massimini, M.
Di Lazzaro, V.
Assenza, G.
EEG spectral exponent as a synthetic index for the longitudinal assessment of stroke recovery
title EEG spectral exponent as a synthetic index for the longitudinal assessment of stroke recovery
title_full EEG spectral exponent as a synthetic index for the longitudinal assessment of stroke recovery
title_fullStr EEG spectral exponent as a synthetic index for the longitudinal assessment of stroke recovery
title_full_unstemmed EEG spectral exponent as a synthetic index for the longitudinal assessment of stroke recovery
title_short EEG spectral exponent as a synthetic index for the longitudinal assessment of stroke recovery
title_sort eeg spectral exponent as a synthetic index for the longitudinal assessment of stroke recovery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038588/
https://www.ncbi.nlm.nih.gov/pubmed/35303540
http://dx.doi.org/10.1016/j.clinph.2022.02.022
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