Abnormal Phase Coupling in Parkinson’s Disease and Normalization Effects of Subthreshold Vestibular Stimulation

The human brain is a highly dynamic structure requiring dynamic coordination between different neural systems to perform numerous cognitive and behavioral tasks. Emerging perspectives on basal ganglia (BG) and thalamic functions have highlighted their role in facilitating and mediating information t...

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Main Authors: Soojin Lee, Aiping Liu, Z. Jane Wang, Martin J. McKeown
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-04-01
Series:Frontiers in Human Neuroscience
Subjects:
EEG
Online Access:https://www.frontiersin.org/article/10.3389/fnhum.2019.00118/full
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spelling doaj-3ed5ccf522504f5d84a0dc467b785a072020-11-25T02:38:57ZengFrontiers Media S.A.Frontiers in Human Neuroscience1662-51612019-04-011310.3389/fnhum.2019.00118438267Abnormal Phase Coupling in Parkinson’s Disease and Normalization Effects of Subthreshold Vestibular StimulationSoojin Lee0Soojin Lee1Aiping Liu2Aiping Liu3Z. Jane Wang4Z. Jane Wang5Martin J. McKeown6Martin J. McKeown7School of Biomedical Engineering, University of British Columbia, Vancouver, BC, CanadaPacific Parkinson’s Research Centre, Vancouver, BC, CanadaPacific Parkinson’s Research Centre, Vancouver, BC, CanadaDepartment of Electronic Science and Technology, University of Science and Technology of China, Hefei, ChinaSchool of Biomedical Engineering, University of British Columbia, Vancouver, BC, CanadaDepartment of Electrical and Computer Engineering, University of British Columbia, Vancouver, BC, CanadaPacific Parkinson’s Research Centre, Vancouver, BC, CanadaDepartment of Medicine (Neurology), University of British Columbia, Vancouver, BC, CanadaThe human brain is a highly dynamic structure requiring dynamic coordination between different neural systems to perform numerous cognitive and behavioral tasks. Emerging perspectives on basal ganglia (BG) and thalamic functions have highlighted their role in facilitating and mediating information transmission among cortical regions. Thus, changes in BG and thalamic structures can induce aberrant modulation of cortico-cortical interactions. Recent work in deep brain stimulation (DBS) has demonstrated that externally applied electrical current to BG structures can have multiple downstream effects in large-scale brain networks. In this work, we identified EEG-based altered resting-state cortical functional connectivity in Parkinson’s disease (PD) and examined effects of dopaminergic medication and electrical vestibular stimulation (EVS), a non-invasive brain stimulation (NIBS) technique capable of stimulating the BG and thalamus through vestibular pathways. Resting EEG was collected from 16 PD subjects and 18 age-matched, healthy controls (HC) in four conditions: sham (no stimulation), EVS1 (4–8 Hz multisine), EVS2 (50–100 Hz multisine) and EVS3 (100–150 Hz multisine). The mean, variability, and entropy were extracted from time-varying phase locking value (PLV), a non-linear measure of pairwise functional connectivity, to probe abnormal cortical couplings in the PD subjects. We found the mean PLV of Cz and C3 electrodes were important for discrimination between PD and HC subjects. In addition, the PD subjects exhibited lower variability and entropy of PLV (mostly in theta and alpha bands) compared to the controls, which were correlated with their clinical characteristics. While levodopa medication was effective in normalizing the mean PLV only, all EVS stimuli normalized the mean, variability and entropy of PLV in the PD subject, with the exact extent and duration of improvement a function of stimulus type. These findings provide evidence demonstrating both low- and high-frequency EVS exert widespread influences on cortico-cortical connectivity, likely via subcortical activation. The improvement observed in PD in a stimulus-dependent manner suggests that EVS with optimized parameters may provide a new non-invasive means for neuromodulation of functional brain networks.https://www.frontiersin.org/article/10.3389/fnhum.2019.00118/fullParkinson’s diseaseelectrical vestibular stimulationEEGphase locking valuecortical oscillationssample entropy
collection DOAJ
language English
format Article
sources DOAJ
author Soojin Lee
Soojin Lee
Aiping Liu
Aiping Liu
Z. Jane Wang
Z. Jane Wang
Martin J. McKeown
Martin J. McKeown
spellingShingle Soojin Lee
Soojin Lee
Aiping Liu
Aiping Liu
Z. Jane Wang
Z. Jane Wang
Martin J. McKeown
Martin J. McKeown
Abnormal Phase Coupling in Parkinson’s Disease and Normalization Effects of Subthreshold Vestibular Stimulation
Frontiers in Human Neuroscience
Parkinson’s disease
electrical vestibular stimulation
EEG
phase locking value
cortical oscillations
sample entropy
author_facet Soojin Lee
Soojin Lee
Aiping Liu
Aiping Liu
Z. Jane Wang
Z. Jane Wang
Martin J. McKeown
Martin J. McKeown
author_sort Soojin Lee
title Abnormal Phase Coupling in Parkinson’s Disease and Normalization Effects of Subthreshold Vestibular Stimulation
title_short Abnormal Phase Coupling in Parkinson’s Disease and Normalization Effects of Subthreshold Vestibular Stimulation
title_full Abnormal Phase Coupling in Parkinson’s Disease and Normalization Effects of Subthreshold Vestibular Stimulation
title_fullStr Abnormal Phase Coupling in Parkinson’s Disease and Normalization Effects of Subthreshold Vestibular Stimulation
title_full_unstemmed Abnormal Phase Coupling in Parkinson’s Disease and Normalization Effects of Subthreshold Vestibular Stimulation
title_sort abnormal phase coupling in parkinson’s disease and normalization effects of subthreshold vestibular stimulation
publisher Frontiers Media S.A.
series Frontiers in Human Neuroscience
issn 1662-5161
publishDate 2019-04-01
description The human brain is a highly dynamic structure requiring dynamic coordination between different neural systems to perform numerous cognitive and behavioral tasks. Emerging perspectives on basal ganglia (BG) and thalamic functions have highlighted their role in facilitating and mediating information transmission among cortical regions. Thus, changes in BG and thalamic structures can induce aberrant modulation of cortico-cortical interactions. Recent work in deep brain stimulation (DBS) has demonstrated that externally applied electrical current to BG structures can have multiple downstream effects in large-scale brain networks. In this work, we identified EEG-based altered resting-state cortical functional connectivity in Parkinson’s disease (PD) and examined effects of dopaminergic medication and electrical vestibular stimulation (EVS), a non-invasive brain stimulation (NIBS) technique capable of stimulating the BG and thalamus through vestibular pathways. Resting EEG was collected from 16 PD subjects and 18 age-matched, healthy controls (HC) in four conditions: sham (no stimulation), EVS1 (4–8 Hz multisine), EVS2 (50–100 Hz multisine) and EVS3 (100–150 Hz multisine). The mean, variability, and entropy were extracted from time-varying phase locking value (PLV), a non-linear measure of pairwise functional connectivity, to probe abnormal cortical couplings in the PD subjects. We found the mean PLV of Cz and C3 electrodes were important for discrimination between PD and HC subjects. In addition, the PD subjects exhibited lower variability and entropy of PLV (mostly in theta and alpha bands) compared to the controls, which were correlated with their clinical characteristics. While levodopa medication was effective in normalizing the mean PLV only, all EVS stimuli normalized the mean, variability and entropy of PLV in the PD subject, with the exact extent and duration of improvement a function of stimulus type. These findings provide evidence demonstrating both low- and high-frequency EVS exert widespread influences on cortico-cortical connectivity, likely via subcortical activation. The improvement observed in PD in a stimulus-dependent manner suggests that EVS with optimized parameters may provide a new non-invasive means for neuromodulation of functional brain networks.
topic Parkinson’s disease
electrical vestibular stimulation
EEG
phase locking value
cortical oscillations
sample entropy
url https://www.frontiersin.org/article/10.3389/fnhum.2019.00118/full
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