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Abstract
Patients suffering from debilitating neurodegenerative diseases often lose the ability to communicate, detrimentally affecting their quality of life. One solution to restore communication is to decode signals directly from the brain to enable neural speech prostheses. However, decoding has been limited by coarse neural recordings which inadequately capture the rich spatio-temporal structure of human brain signals. To resolve this limitation, we performed high-resolution, micro-electrocorticographic (µECoG) neural recordings during intra-operative speech production. We obtained neural signals with 57× higher spatial resolution and 48% higher signal-to-noise ratio compared to macro-ECoG and SEEG. This increased signal quality improved decoding by 35% compared to standard intracranial signals. Accurate decoding was dependent on the high-spatial resolution of the neural interface. Non-linear decoding models designed to utilize enhanced spatio-temporal neural information produced better results than linear techniques. We show that high-density µECoG can enable high-quality speech decoding for future neural speech prostheses.
Previous work has shown speech decoding in the human brain for the development of neural speech prostheses. Here the authors show that high density µECoG electrodes can record at micro-scale spatial resolution to improve neural speech decoding.
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1 Duke University, Department of Biomedical Engineering, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961)
2 Duke School of Medicine, Department of Neurosurgery, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961); University of Utah, Department of Neurosurgery, Clinical Neuroscience Center, Salt Lake City, USA (GRID:grid.223827.e) (ISNI:0000 0001 2193 0096)
3 Duke School of Medicine, Department of Neurosurgery, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961); Duke School of Medicine, Duke Comprehensive Epilepsy Center, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961)
4 Duke School of Medicine, Department of Neurosurgery, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961)
5 Duke University, Department of Biomedical Engineering, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961); Duke School of Medicine, Department of Neurosurgery, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961); Duke School of Medicine, Duke Comprehensive Epilepsy Center, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961); Duke School of Medicine, Department of Neurobiology, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961)
6 University of Pennsylvania, Penn Epilepsy Center, Perelman School of Medicine, Philadelphia, USA (GRID:grid.25879.31) (ISNI:0000 0004 1936 8972)
7 Duke University, Department of Biomedical Engineering, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961); Duke School of Medicine, Department of Neurosurgery, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961); Duke School of Medicine, Duke Comprehensive Epilepsy Center, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961); Duke School of Medicine, Department of Neurology, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961); Duke University, Department of Psychology and Neuroscience, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961); Duke University, Center for Cognitive Neuroscience, Durham, USA (GRID:grid.26009.3d) (ISNI:0000 0004 1936 7961)