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Stability of ECoG High Gamma Signals During Speech and Implications for a Speech BCI System in an Individual with ALS: a Year-long Longitudinal Study

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Journal J Neural Eng
Date 2024 Jun 26
PMID 38925110
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Abstract

Speech brain-computer interfaces (BCIs) have the potential to augment communication in individuals with impaired speech due to muscle weakness, for example in amyotrophic lateral sclerosis (ALS) and other neurological disorders. However, to achieve long-term, reliable use of a speech BCI, it is essential for speech-related neural signal changes to be stable over long periods of time. Here we study, for the first time, the stability of speech-related electrocorticographic (ECoG) signals recorded from a chronically implanted ECoG BCI over a 12 month period.ECoG signals were recorded by an ECoG array implanted over the ventral sensorimotor cortex in a clinical trial participant with ALS. Because ECoG-based speech decoding has most often relied on broadband high gamma (HG) signal changes relative to baseline (non-speech) conditions, we studied longitudinal changes of HG band power at baseline and during speech, and we compared these with residual high frequency noise levels at baseline. Stability was further assessed by longitudinal measurements of signal-to-noise ratio, activation ratio, and peak speech-related HG response magnitude (HG response peaks). Lastly, we analyzed the stability of the event-related HG power changes (HG responses) for individual syllables at each electrode.We found that speech-related ECoG signal responses were stable over a range of syllables activating different articulators for the first year after implantation.Together, our results indicate that ECoG can be a stable recording modality for long-term speech BCI systems for those living with severe paralysis.ClinicalTrials.gov, registration number NCT03567213.

Citing Articles

Real-time detection of spoken speech from unlabeled ECoG signals: A pilot study with an ALS participant.

Angrick M, Luo S, Rabbani Q, Joshi S, Candrea D, Milsap G medRxiv. 2024; .

PMID: 39371161 PMC: 11451764. DOI: 10.1101/2024.09.18.24313755.

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