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Duque, Juliano J.

Mayo Clinic

Mayo Clinic

Citations 3

Phase-Amplitude Coupling Localizes Pathologic Brain with Aid of Behavioral Staging in Sleep
Křemen, Václav , Brinkmann, Benjamin H. , Duque, Juliano J., Carvalho, Diego Z. , Stead, Matt, Berry, Brent , Varatharajah, Yogatheesan , Kucewicz, Michal, Guragain, Hari, Brinkmann, Benjamin, Duque, Juliano, Brinkmann, Benjamin H , Kremen, Vaclav , Carvalho, Diego Z , Kucewicz, Michał T. , Guragain, Hari, Sieck, Gary C. , Worrell, Gregory A.

Life | May 16, 2023 | Volume: 13 | Issue: 5 | Pages: 1186

10.3390/life13051186 Get It

Low frequency brain rhythms facilitate communication across large spatial regions in the brain and high frequency rhythms are thought to signify local processing among nearby assemblies. A heavily investigated mode by which these low frequency and high frequency phenomenon interact is phase-amplitude coupling (PAC). This phenomenon has recently shown promise as a novel electrophysiologic biomarker, in a number of neurologic diseases including human epilepsy. In 17 medically refractory epilepsy patients undergoing phase-2 monitoring for the evaluation of surgical resection and in whom temporal depth electrodes were implanted, we investigated the electrophysiologic relationships of PAC in epileptogenic (seizure onset zone or SOZ) and non-epileptogenic tissue (non-SOZ). That this biomarker can differentiate seizure onset zone from non-seizure onset zone has been established with ictal and pre-ictal data, but less so with interictal data. Here we show that this biomarker can differentiate SOZ from non-SOZ interictally and is also a function of interictal epileptiform discharges. We also show a differential level of PAC in slow-wave-sleep relative to NREM1-2 and awake states. Lastly, we show AUROC evaluation of the localization of SOZ is optimal when utilizing beta or alpha phase onto high-gamma or ripple band. The results suggest an elevated PAC may reflect an electrophysiology-based biomarker for abnormal/epileptogenic brain regions.
Behavioral state classification in epileptic brain using intracranial electrophysiology
Křemen, Václav , Duque, Juliano J., Brinkmann, Benjamin H. , Berry, Brent , Kucewicz, Michał T. , Khadjevand, Fatemeh, Stead, Matt, Louis, Erik K. St. , Berry, Brent M, Van Gompel, Jamie, St Louis, Erik K, Gompel, Jamie J. Van , Worrell, Gregory A. , St Louis, E K , Brinkmann, Benjamin H , Kremen, Vaclav , Kucewicz, Michal

Journal of Neural Engineering | January 4, 2017 | Volume: 14 | Issue: 2 | Pages: 026001

10.1088/1741-2552/aa5688 Get It

Abstract Objective . Automated behavioral state classification can benefit next generation implantable epilepsy devices. In this study we explored the feasibility of automated awake (AW) and slow wave sleep (SWS) classification using wide bandwidth intracranial EEG (iEEG) in patients undergoing evaluation for epilepsy surgery. Approach . Data from seven patients (age 34 ± 12 , 4 women) who underwent intracranial depth electrode implantation for iEEG monitoring were included. Spectral power features (0.1–600 Hz) spanning several frequency bands from a single electrode were used to train and test a support vector machine classifier. Main results . Classification accuracy of 97.8 ± 0.3% (normal tissue) and 89.4 ± 0.8% (epileptic tissue) across seven subjects using multiple spectral power features from a single electrode was achieved. Spectral power features from electrodes placed in normal temporal neocortex were found to be more useful (accuracy 90.8 ± 0.8%) for sleep-wake state classification than electrodes located in normal hippocampus (87.1 ± 1.6%). Spectral power in high frequency band features (Ripple (80–250 Hz), Fast Ripple (250–600 Hz)) showed comparable performance for AW and SWS classification as the best performing Berger bands (Alpha, Beta, low Gamma) with accuracy ⩾90% using a single electrode contact and single spectral feature. Significance . Automated classification of wake and SWS should prove useful for future implantable epilepsy devices with limited computational power, memory, and number of electrodes. Applications include quantifying patient sleep patterns and behavioral state dependent detection, prediction, and electrical stimulation therapies.
The functional organization of human epileptic hippocampus
Klimeš, Petr , Duque, Juliano J., Brinkmann, Benjamin H. , Stead, Matt, Louis, Erik K. St. , Halámek, Josef , Jurák, Pavel , Brinkmann, Ben, Van Gompel, Jamie, St Louis, Erik K, Gompel, Jamie J. Van , Worrell, Gregory A. , St Louis, E K , Brinkmann, Benjamin H , Klimes, Petr

Journal of Neurophysiology | March 31, 2016 | Volume: 115 | Issue: 6 | Pages: 3140-3145

10.1152/jn.00089.2016 Get It

The function and connectivity of human brain is disrupted in epilepsy. We previously reported that the region of epileptic brain generating focal seizures, i.e., the seizure onset zone (SOZ), is functionally isolated from surrounding brain regions in focal neocortical epilepsy. The modulatory effect of behavioral state on the spatial and spectral scales over which the reduced functional connectivity occurs, however, is unclear. Here we use simultaneous sleep staging from scalp EEG with intracranial EEG recordings from medial temporal lobe to investigate how behavioral state modulates the spatial and spectral scales of local field potential synchrony in focal epileptic hippocampus. The local field spectral power and linear correlation between adjacent electrodes provide measures of neuronal population synchrony at different spatial scales, ∼1 and 10 mm, respectively. Our results show increased connectivity inside the SOZ and low connectivity between electrodes in SOZ and outside the SOZ. During slow-wave sleep, we observed decreased connectivity for ripple and fast ripple frequency bands within the SOZ at the 10 mm spatial scale, while the local synchrony remained high at the 1 mm spatial scale. Further study of these phenomena may prove useful for SOZ localization and help understand seizure generation, and the functional deficits seen in epileptic eloquent cortex.