Shared Spectral Parameters Between EEG and Basal Ganglia LFP Distinguish Sleep‐Specific Oscillations in Parkinson's Disease

BACKGROUND: In Parkinson's disease (PD), sleep-related oscillatory dynamics between basal ganglia and cortical nodes may inform sleep dysfunction. The subthalamic nucleus (STN) is highly interconnected with human sleep circuitry and is a current target of interest for sleep neuromodulation. METHODS: To investigate correlated cortical-subcortical activity, we recorded simultaneous PSG and STN local field potentials (LFP) in 19 patients undergoing deep brain stimulation (DBS) for PD. We evaluated the correlation in spectral power between STN-LFP and EEG during polysomnogram (PSG)-defined stages of sleep. In addition, we analyzed aperiodic 1/f spectral parameters (exponent and offset), which have been identified as markers of arousal across sleep stages. Finally, we trained classifiers on aperiodic features to test whether 1/f structure alone could recover PSG-defined sleep stages from EEG and STN-LFP. RESULTS: Results revealed a significant interaction between recording modality and sleep stage. During wakefulness and REM sleep, STN-LFP exhibited a significantly steeper spectral slope compared to scalp EEG. However, this dissociation diminished with sleep depth; slopes appeared more similar during N2 and reversed during N3, where EEG became steeper than LFP. Across subjects, the aperiodic component showed robust state dependence and modality differences with STN-LFP maintaining higher exponents overall. STN-LFP aperiodic features alone classified sleep stages above chance and outperformed scalp EEG, approaching the combined-modality ceiling. CONCLUSION: These findings highlight distinct subcortical electrophysiological signatures in sleep-dependent regulation of neural arousal across brain networks in PD. These insights offer potential biomarkers for both invasive and non-invasive forms of closed-loop neuromodulation strategies targeting sleep dysfunction. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT04620551.

Authors

Institutions

Publication Details

Journal
European Journal of Neurology
Published
2026-08-26
DOI
https://doi.org/10.1111/ene.70733
Primary Topic
Neurological disorders and treatments
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Shared Spectral Parameters Between EEG and Basal Ganglia LFP Distinguish Sleep‐Specific Oscillations in Parkinson's Disease

S. Gliske, Aviva Abosch, John A. Thompson, Casey H. Halpern et al.
European Journal of Neurology
Neurological disorders and treatments
article

Shared Spectral Parameters Between EEG and Basal Ganglia LFP Distinguish Sleep‐Specific Oscillations in Parkinson's Disease

S. Gliske, Aviva Abosch, John A. Thompson, Casey H. Halpern, Lisa Hirt, Siqun Tang, Younghoon Nho, Michael Summers, Dulce Maroni, Lesile West, Ruby Martini, Clete Kushida
article en

Abstract

BACKGROUND: In Parkinson's disease (PD), sleep-related oscillatory dynamics between basal ganglia and cortical nodes may inform sleep dysfunction. The subthalamic nucleus (STN) is highly interconnected with human sleep circuitry and is a current target of interest for sleep neuromodulation. METHODS: To investigate correlated cortical-subcortical activity, we recorded simultaneous PSG and STN local field potentials (LFP) in 19 patients undergoing deep brain stimulation (DBS) for PD. We evaluated the correlation in spectral power between STN-LFP and EEG during polysomnogram (PSG)-defined stages of sleep. In addition, we analyzed aperiodic 1/f spectral parameters (exponent and offset), which have been identified as markers of arousal across sleep stages. Finally, we trained classifiers on aperiodic features to test whether 1/f structure alone could recover PSG-defined sleep stages from EEG and STN-LFP. RESULTS: Results revealed a significant interaction between recording modality and sleep stage. During wakefulness and REM sleep, STN-LFP exhibited a significantly steeper spectral slope compared to scalp EEG. However, this dissociation diminished with sleep depth; slopes appeared more similar during N2 and reversed during N3, where EEG became steeper than LFP. Across subjects, the aperiodic component showed robust state dependence and modality differences with STN-LFP maintaining higher exponents overall. STN-LFP aperiodic features alone classified sleep stages above chance and outperformed scalp EEG, approaching the combined-modality ceiling. CONCLUSION: These findings highlight distinct subcortical electrophysiological signatures in sleep-dependent regulation of neural arousal across brain networks in PD. These insights offer potential biomarkers for both invasive and non-invasive forms of closed-loop neuromodulation strategies targeting sleep dysfunction. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT04620551.

European Journal of NeurologyVol. 33(9)
Baptist Hospital of Miami (US), Nebraska Medical Center (US), University of California, San Francisco (US), Stanford Medicine (US), University of Colorado Anschutz Medical Campus (US), University of Nebraska Medical Center (US), University of Pennsylvania (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 10%
Neurological disorders and treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.