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Electroencephalography-driven approach to prodromal Alzheimer’s disease diagnosis: from biomarker integration to network-level comprehension
Decay of the temporoparietal cortex is associated with prodromal Alzheimer’s disease (AD). Additionally, shrinkage of the temporoparietal cerebral area has been connected with an increase in α3/α2 electroencephalogram (EEG) power ratio in prodromal AD. Furthermore, a lower regional blood perfusion h...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939982/ https://www.ncbi.nlm.nih.gov/pubmed/27462146 http://dx.doi.org/10.2147/CIA.S103313 |
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author | Moretti, Davide Vito |
author_facet | Moretti, Davide Vito |
author_sort | Moretti, Davide Vito |
collection | PubMed |
description | Decay of the temporoparietal cortex is associated with prodromal Alzheimer’s disease (AD). Additionally, shrinkage of the temporoparietal cerebral area has been connected with an increase in α3/α2 electroencephalogram (EEG) power ratio in prodromal AD. Furthermore, a lower regional blood perfusion has been exhibited in patients with a higher α3/α2 proportion when contrasted with low α3/α2 proportion. Furthermore, a lower regional blood perfusion and reduced hippocampal volume has been exhibited in patients with higher α3/α2 when contrasted with lower α3/α2 EEG power ratio. Neuropsychological evaluation, EEG recording, and magnetic resonance imaging were conducted in 74 patients with mild cognitive impairment (MCI). Estimation of cortical thickness and α3/α2 frequency power ratio was conducted for each patient. A subgroup of 27 patients also underwent single-photon emission computed tomography evaluation. In view of α3/α2 power ratio, the patients were divided into three groups. The connections among cortical decay, cerebral perfusion, and memory loss were evaluated by Pearson’s r coefficient. Results demonstrated that higher α3/α2 frequency power ratio group was identified with brain shrinkage and cutdown perfusion inside the temporoparietal projections. In addition, decay and cutdown perfusion rate were connected with memory shortfalls in patients with MCI. MCI subgroup with higher α3/α2 EEG power ratio are at a greater risk to develop AD dementia. |
format | Online Article Text |
id | pubmed-4939982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49399822016-07-26 Electroencephalography-driven approach to prodromal Alzheimer’s disease diagnosis: from biomarker integration to network-level comprehension Moretti, Davide Vito Clin Interv Aging Original Research Decay of the temporoparietal cortex is associated with prodromal Alzheimer’s disease (AD). Additionally, shrinkage of the temporoparietal cerebral area has been connected with an increase in α3/α2 electroencephalogram (EEG) power ratio in prodromal AD. Furthermore, a lower regional blood perfusion has been exhibited in patients with a higher α3/α2 proportion when contrasted with low α3/α2 proportion. Furthermore, a lower regional blood perfusion and reduced hippocampal volume has been exhibited in patients with higher α3/α2 when contrasted with lower α3/α2 EEG power ratio. Neuropsychological evaluation, EEG recording, and magnetic resonance imaging were conducted in 74 patients with mild cognitive impairment (MCI). Estimation of cortical thickness and α3/α2 frequency power ratio was conducted for each patient. A subgroup of 27 patients also underwent single-photon emission computed tomography evaluation. In view of α3/α2 power ratio, the patients were divided into three groups. The connections among cortical decay, cerebral perfusion, and memory loss were evaluated by Pearson’s r coefficient. Results demonstrated that higher α3/α2 frequency power ratio group was identified with brain shrinkage and cutdown perfusion inside the temporoparietal projections. In addition, decay and cutdown perfusion rate were connected with memory shortfalls in patients with MCI. MCI subgroup with higher α3/α2 EEG power ratio are at a greater risk to develop AD dementia. Dove Medical Press 2016-07-06 /pmc/articles/PMC4939982/ /pubmed/27462146 http://dx.doi.org/10.2147/CIA.S103313 Text en © 2016 Moretti. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Moretti, Davide Vito Electroencephalography-driven approach to prodromal Alzheimer’s disease diagnosis: from biomarker integration to network-level comprehension |
title | Electroencephalography-driven approach to prodromal Alzheimer’s disease diagnosis: from biomarker integration to network-level comprehension |
title_full | Electroencephalography-driven approach to prodromal Alzheimer’s disease diagnosis: from biomarker integration to network-level comprehension |
title_fullStr | Electroencephalography-driven approach to prodromal Alzheimer’s disease diagnosis: from biomarker integration to network-level comprehension |
title_full_unstemmed | Electroencephalography-driven approach to prodromal Alzheimer’s disease diagnosis: from biomarker integration to network-level comprehension |
title_short | Electroencephalography-driven approach to prodromal Alzheimer’s disease diagnosis: from biomarker integration to network-level comprehension |
title_sort | electroencephalography-driven approach to prodromal alzheimer’s disease diagnosis: from biomarker integration to network-level comprehension |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939982/ https://www.ncbi.nlm.nih.gov/pubmed/27462146 http://dx.doi.org/10.2147/CIA.S103313 |
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