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Klassen, Bryan

Mayo Clinic

Mayo Clinic

Citations 3

Evoked Resonant Neural Activity Supports Physiology-Guided Asleep Deep Brain Stimulation
Ince, Nuri F. , Branco, Luciano R F., Heydari, Hossein, Swamy, Chandra Prakash , Vanegas-Arroyave, Nora, Tarakad, Arjun , Taneff, Lisa, Bellows, Steven, Anandan, Charenya, Palit, Sandhya, Ruether, Emily, Ali, Rushna , Miller, Kai J. , Klassen, Bryan, Viswanathan, Ashwin , Branco, Luciano, Vanegas‐Arroyave, Nora , Taneff, Lisa Yutong, Bellows, Steven T. , Anandan, Charenya

No container title available | August 18, 2026 | Volume: No volume available | Issue: No issue available | Pages: No page available

10.21203/rs.3.rs-10483928/v1 Get It

Abstract General anesthesia increasingly facilitates asleep deep brain stimulation (DBS) surgery but suppresses spontaneous electrophysiological signals used to guide lead placement. Here, we investigated whether evoked resonant neural activity (ERNA), a stimulation-evoked biomarker of basal ganglia circuitry, remains informative during asleep DBS. We analyzed intraoperative recordings from a multisite cohort of 45 patients (86 hemispheres) undergoing subthalamic nucleus or globus pallidus internus DBS under awake and anesthetized conditions. Anesthesia markedly attenuated spontaneous beta and high-frequency oscillatory activity. Although ERNA amplitude was reduced at matched stimulation intensities, increasing stimulation current restored high-amplitude, spatially localized responses while preserving anatomical specificity. Across both targets, ERNA spatial distributions remained stable across awake and anesthetized states, co-localized with established motor-network biomarkers, and retrospectively identified electrode levels associated with the greatest postoperative therapeutic window. These retrospective findings position stimulation-evoked circuit interrogation as a complement to imaging for physiology-guided asleep DBS and as a candidate signal for contact prioritization. Prospective studies are warranted to determine whether ERNA-guided decisions improve placement, programming efficiency and clinical outcomes.
Paroxysmal facial movements in multiple sclerosis
Ikram, Samar, Aboseif, Albert , Klassen, Bryan T. , Keegan, B. Mark , Banks, Samantha A. , Klassen, Bryan, Keegan, B Mark , Aboseif, Albert

Practical Neurology | December 12, 2025 | Volume: 26 | Issue: 4 | Pages: 405-407

10.1136/pn-2025-004734 Get It

Anterior nucleus of the thalamus seizure detection in ambulatory humans
Gregg, Nicholas M. , Marks, Victoria S. , Sladky, Vladimir , Lundstrom, Brian N. , Klassen, Bryan T. , Brinkmann, Benjamin H. , Miller, Kai J. , Gompel, Jamie J. Van , Křemen, Václav , Klassen, Bryan, Messina, Steven A. , Brinkmann, Benjamin H , Van Gompel, Jamie J , Worrell, Gregory A , Kremen, Vaclav , Lundstrom, Brian Nils , Gregg, Nicholas M , Marks, Victoria S , Worrell, Gregory A.

Epilepsia | August 21, 2021 | Volume: 62 | Issue: 10 | Pages: No page available

10.1111/epi.17047 Get It

AbstractThere is a paucity of data to guide anterior nucleus of the thalamus (ANT) deep brain stimulation (DBS) with brain sensing. The clinical Medtronic Percept DBS device provides constrained brain sensing power within a frequency band (power‐in‐band [PIB]), recorded in 10‐min averaged increments. Here, four patients with temporal lobe epilepsy were implanted with an investigational device providing full bandwidth chronic intracranial electroencephalogram (cEEG) from bilateral ANT and hippocampus (Hc). ANT PIB‐based seizure detection was assessed. Detection parameters were cEEG PIB center frequency, bandwidth, and epoch duration. Performance was evaluated against epileptologist‐confirmed Hc seizures, and assessed by area under the precision‐recall curve (PR‐AUC). Data included 99 days of cEEG, and 20, 278, 3, and 18 Hc seizures for Subjects 1–4. The best detector had 7‐Hz center frequency, 5‐Hz band width, and 10‐s epoch duration (group PR‐AUC = .90), with 75% sensitivity and .38 false alarms per day for Subject 1, and 100% and .0 for Subjects 3 and 4. Hc seizures in Subject 2 did not propagate to ANT. The relative change of ANT PIB was maximal ipsilateral to seizure onset for all detected seizures. Chronic ANT and Hc recordings provide direct guidance for ANT DBS with brain sensing.