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EEG Spectral Features Discriminate between Alzheimer’s and Vascular Dementia
Alzheimer’s disease (AD) and vascular dementia (VaD) present with similar clinical symptoms of cognitive decline, but the underlying pathophysiological mechanisms differ. To determine whether clinical electroencephalography (EEG) can provide information relevant to discriminate between these diagnos...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327579/ https://www.ncbi.nlm.nih.gov/pubmed/25762978 http://dx.doi.org/10.3389/fneur.2015.00025 |
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author | Neto, Emanuel Allen, Elena A. Aurlien, Harald Nordby, Helge Eichele, Tom |
author_facet | Neto, Emanuel Allen, Elena A. Aurlien, Harald Nordby, Helge Eichele, Tom |
author_sort | Neto, Emanuel |
collection | PubMed |
description | Alzheimer’s disease (AD) and vascular dementia (VaD) present with similar clinical symptoms of cognitive decline, but the underlying pathophysiological mechanisms differ. To determine whether clinical electroencephalography (EEG) can provide information relevant to discriminate between these diagnoses, we used quantitative EEG analysis to compare the spectra between non-medicated patients with AD (n = 77) and VaD (n = 77) and healthy elderly normal controls (NC) (n = 77). We use curve-fitting with a combination of a power loss and Gaussian function to model the averaged resting-state spectra of each EEG channel extracting six parameters. We assessed the performance of our model and tested the extracted parameters for group differentiation. We performed regression analysis in a multivariate analysis of covariance with group, age, gender, and number of epochs as predictors and further explored the topographical group differences with pair-wise contrasts. Significant topographical differences between the groups were found in several of the extracted features. Both AD and VaD groups showed increased delta power when compared to NC, whereas the AD patients showed a decrease in alpha power for occipital and temporal regions when compared with NC. The VaD patients had higher alpha power than NC and AD. The AD and VaD groups showed slowing of the alpha rhythm. Variability of the alpha frequency was wider for both AD and VaD groups. There was a general decrease in beta power for both AD and VaD. The proposed model is useful to parameterize spectra, which allowed extracting relevant clinical EEG key features that move toward simple and interpretable diagnostic criteria. |
format | Online Article Text |
id | pubmed-4327579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43275792015-03-11 EEG Spectral Features Discriminate between Alzheimer’s and Vascular Dementia Neto, Emanuel Allen, Elena A. Aurlien, Harald Nordby, Helge Eichele, Tom Front Neurol Neuroscience Alzheimer’s disease (AD) and vascular dementia (VaD) present with similar clinical symptoms of cognitive decline, but the underlying pathophysiological mechanisms differ. To determine whether clinical electroencephalography (EEG) can provide information relevant to discriminate between these diagnoses, we used quantitative EEG analysis to compare the spectra between non-medicated patients with AD (n = 77) and VaD (n = 77) and healthy elderly normal controls (NC) (n = 77). We use curve-fitting with a combination of a power loss and Gaussian function to model the averaged resting-state spectra of each EEG channel extracting six parameters. We assessed the performance of our model and tested the extracted parameters for group differentiation. We performed regression analysis in a multivariate analysis of covariance with group, age, gender, and number of epochs as predictors and further explored the topographical group differences with pair-wise contrasts. Significant topographical differences between the groups were found in several of the extracted features. Both AD and VaD groups showed increased delta power when compared to NC, whereas the AD patients showed a decrease in alpha power for occipital and temporal regions when compared with NC. The VaD patients had higher alpha power than NC and AD. The AD and VaD groups showed slowing of the alpha rhythm. Variability of the alpha frequency was wider for both AD and VaD groups. There was a general decrease in beta power for both AD and VaD. The proposed model is useful to parameterize spectra, which allowed extracting relevant clinical EEG key features that move toward simple and interpretable diagnostic criteria. Frontiers Media S.A. 2015-02-13 /pmc/articles/PMC4327579/ /pubmed/25762978 http://dx.doi.org/10.3389/fneur.2015.00025 Text en Copyright © 2015 Neto, Allen, Aurlien, Nordby and Eichele. 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 Neto, Emanuel Allen, Elena A. Aurlien, Harald Nordby, Helge Eichele, Tom EEG Spectral Features Discriminate between Alzheimer’s and Vascular Dementia |
title | EEG Spectral Features Discriminate between Alzheimer’s and Vascular Dementia |
title_full | EEG Spectral Features Discriminate between Alzheimer’s and Vascular Dementia |
title_fullStr | EEG Spectral Features Discriminate between Alzheimer’s and Vascular Dementia |
title_full_unstemmed | EEG Spectral Features Discriminate between Alzheimer’s and Vascular Dementia |
title_short | EEG Spectral Features Discriminate between Alzheimer’s and Vascular Dementia |
title_sort | eeg spectral features discriminate between alzheimer’s and vascular dementia |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4327579/ https://www.ncbi.nlm.nih.gov/pubmed/25762978 http://dx.doi.org/10.3389/fneur.2015.00025 |
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