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Alzheimer's disease disrupts alpha and beta-band resting-state oscillatory network connectivity

OBJECTIVE: Neuroimaging studies in Alzheimer’s disease (AD) yield conflicting results due to selective investigation. We conducted a comprehensive magnetoencephalography study of connectivity changes in AD and healthy ageing in the resting-state. METHODS: We performed a whole-brain, source-space ass...

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Detalles Bibliográficos
Autores principales: Koelewijn, Loes, Bompas, Aline, Tales, Andrea, Brookes, Matthew J., Muthukumaraswamy, Suresh D., Bayer, Antony, Singh, Krish D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674981/
https://www.ncbi.nlm.nih.gov/pubmed/28571910
http://dx.doi.org/10.1016/j.clinph.2017.04.018
Descripción
Sumario:OBJECTIVE: Neuroimaging studies in Alzheimer’s disease (AD) yield conflicting results due to selective investigation. We conducted a comprehensive magnetoencephalography study of connectivity changes in AD and healthy ageing in the resting-state. METHODS: We performed a whole-brain, source-space assessment of oscillatory neural signalling in multiple frequencies comparing AD patients, elderly and young controls. We compared eyes-open and closed group oscillatory envelope activity in networks obtained through temporal independent component analysis, and calculated whole-brain node-based amplitude and phase connectivity. RESULTS: In bilateral parietotemporal areas, oscillatory envelope amplitude increased with healthy ageing, whereas both local amplitude and node-to-global connectivity decreased with AD. AD-related decreases were spatially specific and restricted to the alpha and beta bands. A significant proportion of the variance in areas of peak group difference was explained by cognitive integrity, in addition to group. None of the groups differed in phase connectivity. Results were highly similar for eyes-open and closed resting-state. CONCLUSIONS: These results support the disconnection syndrome hypothesis and suggest that AD shows distinct and unique patterns of disrupted neural functioning, rather than accelerated healthy ageing. SIGNIFICANCE: Whole-brain assessments show that disrupted regional oscillatory envelope amplitude and connectivity in the alpha and beta bands play a key role in AD.