Cholinergic dysfunction, neurodegeneration, and amyloid-beta pathology in neurodegenerative diseases.
Acetylcholine
Aged
Aged, 80 and over
Alzheimer Disease
/ cerebrospinal fluid
Amyloid beta-Peptides
/ cerebrospinal fluid
Atrophy
Biomarkers
/ cerebrospinal fluid
Brain
/ diagnostic imaging
Cerebral Cortex
/ diagnostic imaging
Cholinergic Antagonists
Cognition
Cross-Sectional Studies
Diagnosis, Differential
Electroencephalography
Female
Hippocampus
/ diagnostic imaging
Humans
Lewy Body Disease
/ cerebrospinal fluid
Magnetic Resonance Imaging
Male
Mental Status and Dementia Tests
Middle Aged
Neurodegenerative Diseases
/ cerebrospinal fluid
Organ Size
Scopolamine
tau Proteins
/ cerebrospinal fluid
Acetylcholine
Alzheimer's disease
Amyloid-beta
Dementia
Electroencephalography
Magnetic resonance imaging
Neurodegeneration
Journal
Psychiatry research. Neuroimaging
ISSN: 1872-7506
Titre abrégé: Psychiatry Res Neuroimaging
Pays: Netherlands
ID NLM: 101723001
Informations de publication
Date de publication:
30 08 2020
30 08 2020
Historique:
received:
27
11
2019
revised:
13
02
2020
accepted:
19
04
2020
pubmed:
9
6
2020
medline:
15
12
2020
entrez:
8
6
2020
Statut:
ppublish
Résumé
Cholinergic dysfunction is central in Alzheimer's disease (AD) and dementia with Lewy bodies (DLB). The electroencephalography-based acetylcholine index (EEG-Ach index) has been proposed as a biomarker of cholinergic dysfunction. However, it is unclear how the EEG-Ach index relates to amyloid-beta pathology and neurodegeneration. We investigated the association between the EEG-Ach index and cerebrospinal fluid (CSF) amyloid-beta, CSF total tau, cortical thickness, and hippocampal volume from magnetic resonance imaging (MRI), and cognition. A total of 127 patients with different neurodegenerative diseases were studied. The EEG-Ach index was calculated from quantitative EEG using statistical pattern recognition. The EEG-Ach index was associated with hippocampal volume and cortical thickness in frontal, temporal, and occipital cortices. Cross-sectional sub-analyses based on a small sample suggests that the EEG-Ach index increases the closest to AD dementia, downstream to amyloid-beta pathology, CSF total tau, and hippocampal volume. We conclude that cholinergic dysfunction correlates with atrophy in brain areas important for AD pathogenesis, and this association is more prominent in the dementia stage. These results together with previous studies from this project suggest that the EEG-Ach index may be a useful biomarker for cholinergic dysfunction, with value for differential diagnosis of dementia and monitoring patients at the dementia stage.
Identifiants
pubmed: 32505903
pii: S0925-4927(20)30071-8
doi: 10.1016/j.pscychresns.2020.111099
pii:
doi:
Substances chimiques
Amyloid beta-Peptides
0
Biomarkers
0
Cholinergic Antagonists
0
tau Proteins
0
Scopolamine
DL48G20X8X
Acetylcholine
N9YNS0M02X
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
111099Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.