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Abstract
Modulating brain oscillations has strong therapeutic potential. Interventions that both non-invasively modulate deep brain structures and are practical for chronic daily home use are desirable for a variety of therapeutic applications. Repetitive audio-visual stimulation, or sensory flicker, is an accessible approach that modulates hippocampus in mice, but its effects in humans are poorly defined. We therefore quantified the neurophysiological effects of flicker with high spatiotemporal resolution in patients with focal epilepsy who underwent intracranial seizure monitoring. In this interventional trial (NCT04188834) with a cross-over design, subjects underwent different frequencies of flicker stimulation in the same recording session with the effect of sensory flicker exposure on local field potential (LFP) power and interictal epileptiform discharges (IEDs) as primary and secondary outcomes, respectively. Flicker focally modulated local field potentials in expected canonical sensory cortices but also in the medial temporal lobe and prefrontal cortex, likely via resonance of stimulated long-range circuits. Moreover, flicker decreased interictal epileptiform discharges, a pathological biomarker of epilepsy and degenerative diseases, most strongly in regions where potentials were flicker-modulated, especially the visual cortex and medial temporal lobe. This trial met the scientific goal and is now closed. Our findings reveal how multi-sensory stimulation may modulate cortical structures to mitigate pathological activity in humans.
Repetitive audio-visual stimulation, or sensory flicker, can modulate oscillations in a non-invasive manner. Here the authors demonstrate the potential of flicker in individuals with epilepsy undergoing intracranial seizure monitoring.
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1 Emory University School of Medicine, Department of Neurosurgery, Atlanta, USA (GRID:grid.189967.8) (ISNI:0000 0001 0941 6502); Emory University, Neuroscience Graduate Program, Graduate Division of Biological and Biomedical Sciences, Atlanta, USA (GRID:grid.189967.8) (ISNI:0000 0004 1936 7398); Georgia Institute of Technology & Emory University, Coulter Department of Biomedical Engineering, Atlanta, USA (GRID:grid.470935.c)
2 Emory University School of Medicine, Department of Neurosurgery, Atlanta, USA (GRID:grid.189967.8) (ISNI:0000 0001 0941 6502); Georgia Institute of Technology & Emory University, Coulter Department of Biomedical Engineering, Atlanta, USA (GRID:grid.470935.c)
3 Emory University School of Medicine, Department of Neurosurgery, Atlanta, USA (GRID:grid.189967.8) (ISNI:0000 0001 0941 6502)
4 Georgia Institute of Technology, Department of Electrical and Computer Engineering, Atlanta, USA (GRID:grid.213917.f) (ISNI:0000 0001 2097 4943)
5 Emory University School of Medicine, Department of Neurosurgery, Atlanta, USA (GRID:grid.189967.8) (ISNI:0000 0001 0941 6502); New Brunswick and New Jersey Medical School, Departments of Neurosurgery and Neuroscience and Cell Biology, Rutgers Robert Wood Johnson Medical School, Newark, USA (GRID:grid.430387.b) (ISNI:0000 0004 1936 8796)
6 Emory University School of Medicine, Department of Neurology, Atlanta, USA (GRID:grid.189967.8) (ISNI:0000 0001 0941 6502)
7 Washington University, Departments of Neurological Surgery, Neurology, Psychiatry, and Biomedical Engineering, St. Louis, USA (GRID:grid.4367.6) (ISNI:0000 0001 2355 7002)
8 Emory University, Neuroscience Graduate Program, Graduate Division of Biological and Biomedical Sciences, Atlanta, USA (GRID:grid.189967.8) (ISNI:0000 0004 1936 7398); Georgia Institute of Technology & Emory University, Coulter Department of Biomedical Engineering, Atlanta, USA (GRID:grid.470935.c)