4.4 Article

Brain Connectivity Alterations Are Associated with the Development of Dementia in Parkinson's Disease

Journal

BRAIN CONNECTIVITY
Volume 6, Issue 3, Pages 216-224

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/brain.2015.0390

Keywords

Parkinson's disease; cognitive decline; delta frequency; gamma frequency; posterior brain regions; resting state EEG

Categories

Funding

  1. Canadian Institutes of Health Research, Canada [MOP-84482]
  2. Fonds de Recherche du Quebec-Sante, Canada
  3. Quebec Network for Research on Aging
  4. Canadian Institutes of Health Research (CIHR)

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Dementia affects a high proportion of Parkinson's disease (PD) patients and poses a burden on caregivers and healthcare services. Electroencephalography (EEG) is a common nonevasive and nonexpensive technique that can easily be used in clinical settings to identify brain functional abnormalities. Only few studies had identified EEG abnormalities that can predict PD patients at higher risk for dementia. Brain connectivity EEG measures, such as multiscale entropy (MSE) and phase-locking value (PLV) analyses, may be more informative and sensitive to brain alterations leading to dementia than previously used methods. This study followed 62 dementia-free PD patients for a mean of 3.4 years to identify cerebral alterations that are associated with dementia. Baseline resting state EEG of patients who developed dementia (N= 18) was compared to those of patients who remained dementia-free (N=44) and of 37 healthy subjects. MSE and PLV analyses were performed. Partial least squares statistical analysis revealed group differences associated with the development of dementia. Patients who developed dementia showed higher signal complexity and lower PLVs in low frequencies (mainly in delta frequency) than patients who remained dementia-free and controls. Conversely, both patient groups showed lower signal variability and higher PLVs in high frequencies (mainly in gamma frequency) compared to controls, with the strongest effect in patients who developed dementia. These findings suggest that specific disruptions of brain communication can be measured before PD patients develop dementia, providing a new potential marker to identify patients at highest risk of developing dementia and who are the best candidates for neuroprotective trials.

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