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Spatio‐spectral relationships between pathological neural dynamics and cognitive impairment along the Alzheimer's disease spectrum

INTRODUCTION: Numerous studies have described aberrant patterns of rhythmic neural activity in patients along the Alzheimer's disease (AD) spectrum, yet the relationships between these pathological features and cognitive decline are uncertain. METHODS: We acquired magnetoencephalography (MEG) d...

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Detalles Bibliográficos
Autores principales: Wiesman, Alex I., Murman, Daniel L., May, Pamela E., Schantell, Mikki, Losh, Rebecca A., Johnson, Hallie J., Willet, Madelyn P., Eastman, Jacob A., Christopher‐Hayes, Nicholas J., Knott, Nichole L., Houseman, Lisa L., Wolfson, Sara L., Losh, Kathryn L., Johnson, Craig M., Wilson, Tony W.
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/PMC8165730/
https://www.ncbi.nlm.nih.gov/pubmed/34095434
http://dx.doi.org/10.1002/dad2.12200
Descripción
Sumario:INTRODUCTION: Numerous studies have described aberrant patterns of rhythmic neural activity in patients along the Alzheimer's disease (AD) spectrum, yet the relationships between these pathological features and cognitive decline are uncertain. METHODS: We acquired magnetoencephalography (MEG) data from 38 amyloid‐PET biomarker‐confirmed patients on the AD spectrum and a comparison group of biomarker‐negative cognitively normal (CN) healthy adults, alongside an extensive neuropsychological battery. RESULTS: By modeling whole‐brain rhythmic neural activity with an extensive neuropsychological profile in patients on the AD spectrum, we show that the spectral and spatial features of deviations from healthy adults in neural population‐level activity inform their relevance to domain‐specific neurocognitive declines. DISCUSSION: Regional oscillatory activity represents a sensitive metric of neuronal pathology in patients on the AD spectrum. By considering not only the spatial, but also the spectral, definitions of cortical neuronal activity, we show that domain‐specific cognitive declines can be better modeled in these individuals.