Multi-approach comparative study of EEG patterns associated with the most common forms of dementia.

Dementia Differential diagnosis Electroencephalography Functional connectivity Micro-state analysis Spectral analysis

Journal

Neurobiology of aging
ISSN: 1558-1497
Titre abrégé: Neurobiol Aging
Pays: United States
ID NLM: 8100437

Informations de publication

Date de publication:
10 2023
Historique:
received: 13 12 2022
revised: 30 05 2023
accepted: 10 06 2023
medline: 14 8 2023
pubmed: 12 7 2023
entrez: 11 7 2023
Statut: ppublish

Résumé

Electroencephalography's (EEG) sensitivity in discriminating dementia syndromes remains unclear. This study aimed to investigate EEG markers in patients with major cognitive disorders. The studied population included 4 groups of patients: Alzheimer's disease with associated vascular lesions, Alzheimer's disease without vascular lesions (AD-V), Lewy body disease and vascular dementia (VaD); and completed by a control group composed by cognitively unimpaired patients. EEGs were analysed quantitatively using spectral analysis, functional connectivity and micro-states. By comparison to the controls, expected slowing and alterations of functional connectivity were detected in patients with dementia. Among these patients, an overall increase in power in the alpha band was observed in the VaD group, mainly when compared to the 2 AD groups, while the Alzheimer's disease without vascular lesions group exhibited increased power in the beta-2 band and higher functional connectivity in the same frequency band. Micro-state analyses revealed differences in temporal dynamics for the VaD group. A number of EEG modifications reported as markers of some syndromes were found, but others were not reproduced.

Identifiants

pubmed: 37433259
pii: S0197-4580(23)00124-0
doi: 10.1016/j.neurobiolaging.2023.06.008
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

30-39

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest None

Auteurs

Ines Bejia (I)

Univ. Lille, INSERM, U1172 - LilNCog - Lille Neuroscience & Cognition, F-59000 Lille, France.

Jordan Labidi (J)

CHU Lille, Clinical Neurophysiology Department, F-59000 Lille, France.

Aude Warniez (A)

Univ. Lille, INSERM, U1172 - LilNCog - Lille Neuroscience & Cognition, F-59000 Lille, France.

Madli Bayot (M)

Univ. Lille, INSERM, U1172 - LilNCog - Lille Neuroscience & Cognition, F-59000 Lille, France; CHU Lille, Clinical Neurophysiology Department, F-59000 Lille, France.

Jean-Louis Bourriez (JL)

CHU Lille, Clinical Neurophysiology Department, F-59000 Lille, France.

Philippe Derambure (P)

Univ. Lille, INSERM, U1172 - LilNCog - Lille Neuroscience & Cognition, F-59000 Lille, France; CHU Lille, Clinical Neurophysiology Department, F-59000 Lille, France.

Thibaut Lebouvier (T)

Univ. Lille, INSERM, U1172 - LilNCog - Lille Neuroscience & Cognition, F-59000 Lille, France; CHU Lille, Centre Mémoire de Ressources et de Recherche (CMRR), F-59000 Lille, France.

Florence Pasquier (F)

Univ. Lille, INSERM, U1172 - LilNCog - Lille Neuroscience & Cognition, F-59000 Lille, France; CHU Lille, Centre Mémoire de Ressources et de Recherche (CMRR), F-59000 Lille, France.

Arnaud Delval (A)

Univ. Lille, INSERM, U1172 - LilNCog - Lille Neuroscience & Cognition, F-59000 Lille, France; CHU Lille, Clinical Neurophysiology Department, F-59000 Lille, France.

Nacim Betrouni (N)

Univ. Lille, INSERM, U1172 - LilNCog - Lille Neuroscience & Cognition, F-59000 Lille, France. Electronic address: nacim.betrouni@inserm.fr.

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