Evaluation of Parkinsons disease with early diagnosis using single-channel EEG features and auditory cognitive assessment
Parkinsons disease (PD) diagnosis is challenging due to subtle early clinical signs. F-DOPA PET is commonly used for early PD diagnosis. We explore the potential of machine-learning (ML) based EEG features extracted from single-channel EEG during auditory cognitive assessment as a noninvasive, low-c...
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Zusammenfassung: | Parkinsons disease (PD) diagnosis is challenging due to subtle early clinical
signs. F-DOPA PET is commonly used for early PD diagnosis. We explore the
potential of machine-learning (ML) based EEG features extracted from
single-channel EEG during auditory cognitive assessment as a noninvasive,
low-cost support for PD diagnosis. The study included data collected from 32
participants who underwent an F-DOPA PET scan as part of their standard
treatment and 20 cognitively healthy controls. Participants performed an
auditory cognitive assessment recorded with Neurosteer EEG device. Data
processing involved wavelet-packet decomposition and ML. First, a prediction
model was developed to predict 1/3 of the undisclosed F-DOPA results. Then,
generalized linear mixed models were calculated to distinguish between PD and
non-PD subjects on the frequency bands and ML-based EEG features (A0 and L1)
previously associated with cognitive functions. The prediction model accurately
labeled patients with unrevealed scores as positive F-DOPA. Novel EEG feature
A0 and the Delta band showed significant separation between study groups, with
healthy controls exhibiting higher activity than PD patients. EEG feature L1
activity was significantly lower in resting state compared to high-cognitive
load. This effect was absent in the PD group, suggesting that lower activity in
resting state is lacking in PD patients. This study successfully demonstrated
the ability to separate patients with positive vs. negative F-DOPA PET results
with an easy-to-use single-channel EEG during an auditory cognitive assessment.
Future longitudinal studies should further explore the potential utility of
this tool for early PD diagnosis and as a potential biomarker in PD. |
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DOI: | 10.48550/arxiv.2308.03406 |