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Quantitative EEG reflects non-dopaminergic disease severity in Parkinson's disease.

Authors :
Geraedts VJ
Marinus J
Gouw AA
Mosch A
Stam CJ
van Hilten JJ
Contarino MF
Tannemaat MR
Source :
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology [Clin Neurophysiol] 2018 Aug; Vol. 129 (8), pp. 1748-1755. Date of Electronic Publication: 2018 May 29.
Publication Year :
2018

Abstract

Objective: In Parkinson's Disease (PD), measures of non-dopaminergic systems involvement may reflect disease severity and therefore contribute to patient-selection for Deep Brain Stimulation (DBS). There is currently no determinant for non-dopaminergic disease severity. In this exploratory study, we investigated whether quantitative EEG reflects non-dopaminergic disease severity in PD.<br />Methods: Sixty-three consecutive PD patients screened for DBS were included (mean age 62.4 ± 7.2 years, 32% females). Relative spectral powers and the Phase-Lag-Index (PLI) reflecting functional connectivity were analysed on routine EEGs. Non-dopaminergic disease severity was quantified using the SENS-PD score and its subdomains; motor-severity was quantified using the MDS-UPDRS III.<br />Results: The SENS-PD composite score correlated with a spectral ratio ((δ + θ)/(α1 + α2 + β) powers) (global spectral ratio Pearson's r = 0.4, 95% Confidence Interval (95%CI) 0.1-0.6), and PLI in the α2 band (10-13 Hz) (r = -0.3, 95%CI -0.5 to -0.1). These correlations seem driven by the subdomains cognition and psychotic symptoms. MDS-UPDRS III was not significantly correlated with EEG parameters.<br />Conclusions: EEG slowing and reduced functional connectivity in the α2 band were associated with non-dopaminergic disease severity in PD.<br />Significance: The described EEG parameters may have complementary utility as determinants of non-dopaminergic involvement in PD.<br /> (Copyright © 2018 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1872-8952
Volume :
129
Issue :
8
Database :
MEDLINE
Journal :
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
Publication Type :
Academic Journal
Accession number :
29887401
Full Text :
https://doi.org/10.1016/j.clinph.2018.04.752