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Resting-state EEG measures cognitive impairment in Parkinson’s disease

BACKGROUND: Cognitive dysfunction is common in Parkinson’s disease (PD) and is diagnosed by complex, time-consuming psychometric tests which are affected by language and education, subject to learning effects, and not suitable for continuous monitoring of cognition. OBJECTIVES: We developed and eval...

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Detalles Bibliográficos
Autores principales: Anjum, Md Fahim, Espinoza, Arturo, Cole, Rachel, Singh, Arun, May, Patrick, Uc, Ergun, Dasgupta, Soura, Narayanan, Nandakumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055637/
https://www.ncbi.nlm.nih.gov/pubmed/36993450
http://dx.doi.org/10.21203/rs.3.rs-2666578/v1
Descripción
Sumario:BACKGROUND: Cognitive dysfunction is common in Parkinson’s disease (PD) and is diagnosed by complex, time-consuming psychometric tests which are affected by language and education, subject to learning effects, and not suitable for continuous monitoring of cognition. OBJECTIVES: We developed and evaluated an EEG-based biomarker to index cognitive functions in PD from a few minutes of resting-state EEG. METHODS: We hypothesized that synchronous changes in EEG across the power spectrum can measure cognition. We optimized a data-driven algorithm to efficiently capture these changes and index cognitive function in 100 PD and 49 control participants. We compared our EEG-based cognitive index with the Montreal cognitive assessment (MoCA) and cognitive tests across different domains from the National Institutes of Health (NIH) Toolbox using cross-validation schemes, regression models, and randomization tests. RESULTS: We observed cognition-related changes in EEG activities over multiple spectral rhythms. Utilizing only 8 best-performing EEG electrodes, our proposed index strongly correlated with cognition (rho = 0.68, p value < 0.001 with MoCA; rho ≥ 0.56, p value < 0.001 with cognitive tests from the NIH Toolbox) outperforming traditional spectral markers (rho = −0.30 – 0.37). The index showed a strong fit in regression models (R(2) = 0.46) with MoCA, yielded 80% accuracy in detecting cognitive impairment, and was effective in both PD and control participants. CONCLUSIONS: Our approach is computationally efficient for real-time indexing of cognition across domains, implementable even in hardware with limited computing capabilities, making it potentially compatible with dynamic therapies such as closed-loop neurostimulation, and will inform next-generation neurophysiological biomarkers for monitoring cognition in PD and other neurological diseases.