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Correspondence of optimal stimulation and beta power varies regionally in STN DBS for Parkinson disease
Institution:1. “Aldo Ravelli” Center for Neurotechnology and Experimental Brain Therapeutics, University of Milan and Fondazione IRCCS Ca'' Granda - Ospedale Maggiore, Milan, Italy;2. Department of Neuroscience, Istituto di Ricerche Farmacologiche “Mario Negri IRCCS, Milan, Italy;3. Department of Neuroscience, University of Turin, Italy;4. Department of Neuroscience (DNS), University of Padua, Italy;5. Movement Disorder Unit, Department of Clinical Neurosciences, IRCCS Carlo Besta Neurological Institute, Milan, Italy;6. Department of Neurology, “F. Miulli” General Hospital, Acquaviva delle Fonti, Italy;7. Department of Neurology, Parkinson''s Center, IRCCS Neuromed, Pozzilli, Italy;8. Parkinson Unit, IRCCS San Camillo Hospital, Venice, Italy;9. Department of Engineering and Architecture, University of Trieste, Trieste, Italy;10. Parkinson and movement disorders Unit, IRCCS Mondino Foundation, Pavia, Italy;11. Department of Neurology, Villa Margherita, Private clinic, Arcugnano, Vicenza, Italy;12. Department of Health Sciences, University of Milan, San Paolo Hospital, Milan, Italy
Abstract:IntroductionSubthalamic nucleus deep brain stimulation (STN DBS) for Parkinson disease (PD) normalizes neuronal hypersynchrony in the beta frequency range (13–30 Hz). The spatial correspondence of maximal beta power to the site of optimal stimulation along the DBS lead trajectory has been debated.MethodsWe determined the trajectory locations of the active contact, maximal beta power, and the dorsal border of the STN (DB-STN) in DBS patients. Beta power profiles were measured during intraoperative microelectrode recording (MER). Active contact locations were assigned during blinded, postoperative DBS programming. The DB-STN was identified both electrophysiologically during MER and anatomically on MRI. After grouping DBS trajectories into quadrants relative to the anatomic STN midpoint, we examined regional variations in the relative trajectory locations of the three entities.ResultsSTN DBS significantly improved motor performance for all 13 DBS patients, with active contacts at the DB-STN. Along trajectories passing posterior-medial to the STN midpoint, maximal beta power co-localized with active contacts at the DB-STN (difference Δ = 0.4 ± 1.6 mm, p = 0.57). By contrast, in posterior-lateral trajectories, maximal beta arose within the STN, ventral to active contacts (Δ = 1.9 ± 1.3 mm, p = 0.002). For trajectories anterior to the STN midpoint, maximal beta power co-localized with the DB-STN, while active contacts were ventral to peak beta power (p = 0.05).ConclusionOur findings indicate that co-localization of optimal stimulation and beta power varies by anatomical region in STN DBS for Parkinson disease.
Keywords:Deep brain stimulation  Beta oscillations  Parkinson disease  Subthalamic nucleus  Optimal stimulation
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