TY - JOUR
T1 - Seizure occurrence is linked to multiday cycles in diverse physiological signals
AU - Gregg, Nicholas M.
AU - Pal Attia, Tal
AU - Nasseri, Mona
AU - Joseph, Boney
AU - Karoly, Philippa
AU - Cui, Jie
AU - Stirling, Rachel E.
AU - Viana, Pedro F.
AU - Richner, Thomas J.
AU - Nurse, Ewan S.
AU - Schulze-Bonhage, Andreas
AU - Cook, Mark J.
AU - Worrell, Gregory A.
AU - Richardson, Mark P.
AU - Freestone, Dean R.
AU - Brinkmann, Benjamin H.
N1 - Funding Information:
This research was supported by the Epilepsy Foundation Epilepsy Innovation Institute My Seizure Gauge, NIH grants UH3‐NS95495 and R01‐NS09288203, American Epilepsy Society Research and Training Fellowship for Clinicians (N.M.G.), and National Science Foundation grant CBET‐2138378 (M.N.). The authors acknowledge technical and administrative support from Sherry Klingerman CCRP.
Publisher Copyright:
© 2023 International League Against Epilepsy.
PY - 2023
Y1 - 2023
N2 - Objective: The factors that influence seizure timing are poorly understood, and seizure unpredictability remains a major cause of disability. Work in chronobiology has shown that cyclical physiological phenomena are ubiquitous, with daily and multiday cycles evident in immune, endocrine, metabolic, neurological, and cardiovascular function. Additionally, work with chronic brain recordings has identified that seizure risk is linked to daily and multiday cycles in brain activity. Here, we provide the first characterization of the relationships between the cyclical modulation of a diverse set of physiological signals, brain activity, and seizure timing. Methods: In this cohort study, 14 subjects underwent chronic ambulatory monitoring with a multimodal wrist-worn sensor (recording heart rate, accelerometry, electrodermal activity, and temperature) and an implanted responsive neurostimulation system (recording interictal epileptiform abnormalities and electrographic seizures). Wavelet and filter–Hilbert spectral analyses characterized circadian and multiday cycles in brain and wearable recordings. Circular statistics assessed electrographic seizure timing and cycles in physiology. Results: Ten subjects met inclusion criteria. The mean recording duration was 232 days. Seven subjects had reliable electroencephalographic seizure detections (mean = 76 seizures). Multiday cycles were present in all wearable device signals across all subjects. Seizure timing was phase locked to multiday cycles in five (temperature), four (heart rate, phasic electrodermal activity), and three (accelerometry, heart rate variability, tonic electrodermal activity) subjects. Notably, after regression of behavioral covariates from heart rate, six of seven subjects had seizure phase locking to the residual heart rate signal. Significance: Seizure timing is associated with daily and multiday cycles in multiple physiological processes. Chronic multimodal wearable device recordings can situate rare paroxysmal events, like seizures, within a broader chronobiology context of the individual. Wearable devices may advance the understanding of factors that influence seizure risk and enable personalized time-varying approaches to epilepsy care.
AB - Objective: The factors that influence seizure timing are poorly understood, and seizure unpredictability remains a major cause of disability. Work in chronobiology has shown that cyclical physiological phenomena are ubiquitous, with daily and multiday cycles evident in immune, endocrine, metabolic, neurological, and cardiovascular function. Additionally, work with chronic brain recordings has identified that seizure risk is linked to daily and multiday cycles in brain activity. Here, we provide the first characterization of the relationships between the cyclical modulation of a diverse set of physiological signals, brain activity, and seizure timing. Methods: In this cohort study, 14 subjects underwent chronic ambulatory monitoring with a multimodal wrist-worn sensor (recording heart rate, accelerometry, electrodermal activity, and temperature) and an implanted responsive neurostimulation system (recording interictal epileptiform abnormalities and electrographic seizures). Wavelet and filter–Hilbert spectral analyses characterized circadian and multiday cycles in brain and wearable recordings. Circular statistics assessed electrographic seizure timing and cycles in physiology. Results: Ten subjects met inclusion criteria. The mean recording duration was 232 days. Seven subjects had reliable electroencephalographic seizure detections (mean = 76 seizures). Multiday cycles were present in all wearable device signals across all subjects. Seizure timing was phase locked to multiday cycles in five (temperature), four (heart rate, phasic electrodermal activity), and three (accelerometry, heart rate variability, tonic electrodermal activity) subjects. Notably, after regression of behavioral covariates from heart rate, six of seven subjects had seizure phase locking to the residual heart rate signal. Significance: Seizure timing is associated with daily and multiday cycles in multiple physiological processes. Chronic multimodal wearable device recordings can situate rare paroxysmal events, like seizures, within a broader chronobiology context of the individual. Wearable devices may advance the understanding of factors that influence seizure risk and enable personalized time-varying approaches to epilepsy care.
KW - biomarkers
KW - chronobiology
KW - seizure forecasting
KW - wearable devices
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U2 - 10.1111/epi.17607
DO - 10.1111/epi.17607
M3 - Article
C2 - 37060170
AN - SCOPUS:85153384688
SN - 0013-9580
JO - Epilepsia
JF - Epilepsia
ER -