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The predictive value of normal EEGs in dementia due to Alzheimer’s disease

OBJECTIVE: To determine differences in clinical presentation and disease progression between patients with dementia due to AD with visually normal and abnormal EEG recordings. We hypothesized that patients with normal electroencephalographs (EEGs) are a representation of the heterogeneity of AD. We...

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Autores principales: Briels, Casper T., Stam, Cornelis J., Scheltens, Philip, Gouw, Alida A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108419/
https://www.ncbi.nlm.nih.gov/pubmed/33835723
http://dx.doi.org/10.1002/acn3.51339
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author Briels, Casper T.
Stam, Cornelis J.
Scheltens, Philip
Gouw, Alida A.
author_facet Briels, Casper T.
Stam, Cornelis J.
Scheltens, Philip
Gouw, Alida A.
author_sort Briels, Casper T.
collection PubMed
description OBJECTIVE: To determine differences in clinical presentation and disease progression between patients with dementia due to AD with visually normal and abnormal EEG recordings. We hypothesized that patients with normal electroencephalographs (EEGs) are a representation of the heterogeneity of AD. We expected this group to have a phenotype with relatively predominant hippocampal atrophy, memory deficits, and a slower disease progression. METHODS: Patients were included based on diagnosis of dementia due to AD, positive amyloid and tau cerebrospinal fluid (CSF) biomarkers, and the availability of EEG recordings. Patients were categorized in groups of normal (N = 208) and abnormal (N = 336) EEG recordings based on visual assessment by experienced neurophysiologists. At baseline demographics, cognitive, MRI, and CSF measures were compared between groups. Cognitive data from follow‐up visits were assessed by linear mixed‐effects models (LMMs), and corrected for baseline value, sex, age, and educational level, to compare cognitive deterioration over time between groups. RESULTS: About 1 in 4.5 patients with AD dementia had a visually normal EEG and this group showed better overall cognitive performance compared to the abnormal group, where memory was the most prominent affected domain. The normal group showed less global and parietal but similar medial temporal atrophy. Follow‐up data showed a slower deterioration on all tested cognitive domains in the normal EEG group. INTERPRETATION: Patients with dementia due to AD and visually normal EEG recordings showed a milder clinical presentation and had a milder disease progression compared to patients with an abnormal EEG. These results provide evidence of clinical and biological heterogeneity within AD dementia.
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spelling pubmed-81084192021-05-10 The predictive value of normal EEGs in dementia due to Alzheimer’s disease Briels, Casper T. Stam, Cornelis J. Scheltens, Philip Gouw, Alida A. Ann Clin Transl Neurol Research Articles OBJECTIVE: To determine differences in clinical presentation and disease progression between patients with dementia due to AD with visually normal and abnormal EEG recordings. We hypothesized that patients with normal electroencephalographs (EEGs) are a representation of the heterogeneity of AD. We expected this group to have a phenotype with relatively predominant hippocampal atrophy, memory deficits, and a slower disease progression. METHODS: Patients were included based on diagnosis of dementia due to AD, positive amyloid and tau cerebrospinal fluid (CSF) biomarkers, and the availability of EEG recordings. Patients were categorized in groups of normal (N = 208) and abnormal (N = 336) EEG recordings based on visual assessment by experienced neurophysiologists. At baseline demographics, cognitive, MRI, and CSF measures were compared between groups. Cognitive data from follow‐up visits were assessed by linear mixed‐effects models (LMMs), and corrected for baseline value, sex, age, and educational level, to compare cognitive deterioration over time between groups. RESULTS: About 1 in 4.5 patients with AD dementia had a visually normal EEG and this group showed better overall cognitive performance compared to the abnormal group, where memory was the most prominent affected domain. The normal group showed less global and parietal but similar medial temporal atrophy. Follow‐up data showed a slower deterioration on all tested cognitive domains in the normal EEG group. INTERPRETATION: Patients with dementia due to AD and visually normal EEG recordings showed a milder clinical presentation and had a milder disease progression compared to patients with an abnormal EEG. These results provide evidence of clinical and biological heterogeneity within AD dementia. John Wiley and Sons Inc. 2021-04-09 /pmc/articles/PMC8108419/ /pubmed/33835723 http://dx.doi.org/10.1002/acn3.51339 Text en © 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Briels, Casper T.
Stam, Cornelis J.
Scheltens, Philip
Gouw, Alida A.
The predictive value of normal EEGs in dementia due to Alzheimer’s disease
title The predictive value of normal EEGs in dementia due to Alzheimer’s disease
title_full The predictive value of normal EEGs in dementia due to Alzheimer’s disease
title_fullStr The predictive value of normal EEGs in dementia due to Alzheimer’s disease
title_full_unstemmed The predictive value of normal EEGs in dementia due to Alzheimer’s disease
title_short The predictive value of normal EEGs in dementia due to Alzheimer’s disease
title_sort predictive value of normal eegs in dementia due to alzheimer’s disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8108419/
https://www.ncbi.nlm.nih.gov/pubmed/33835723
http://dx.doi.org/10.1002/acn3.51339
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