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Cortical Topography of Error-Related High-Frequency Potentials During Erroneous Control in a Continuous Control Brain–Computer Interface
Brain–computer interfaces (BCIs) benefit greatly from performance feedback, but current systems lack automatic, task-independent feedback. Cortical responses elicited from user error have the potential to serve as state-based feedback to BCI decoders. To gain a better understanding of local error po...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541115/ https://www.ncbi.nlm.nih.gov/pubmed/31191218 http://dx.doi.org/10.3389/fnins.2019.00502 |
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author | Wilson, Nile R. Sarma, Devapratim Wander, Jeremiah D. Weaver, Kurt E. Ojemann, Jeffrey G. Rao, Rajesh P. N. |
author_facet | Wilson, Nile R. Sarma, Devapratim Wander, Jeremiah D. Weaver, Kurt E. Ojemann, Jeffrey G. Rao, Rajesh P. N. |
author_sort | Wilson, Nile R. |
collection | PubMed |
description | Brain–computer interfaces (BCIs) benefit greatly from performance feedback, but current systems lack automatic, task-independent feedback. Cortical responses elicited from user error have the potential to serve as state-based feedback to BCI decoders. To gain a better understanding of local error potentials, we investigate responsive cortical power underlying error-related potentials (ErrPs) from the human cortex during a one-dimensional center-out BCI task, tracking the topography of high-gamma (70–100 Hz) band power (HBP) specific to BCI error. We measured electrocorticography (ECoG) in three human subjects during dynamic, continuous control over BCI cursor velocity. Subjects used motor imagery and rest to move the cursor toward and subsequently dwell within a target region. We then identified and labeled epochs where the BCI decoder incorrectly moved the cursor in the direction opposite of the subject’s expectations (i.e., BCI error). We found increased HBP in various cortical areas 100–500 ms following BCI error with respect to epochs of correct, intended control. Significant responses were noted in primary somatosensory, motor, premotor, and parietal areas and generally regardless of whether the subject was using motor imagery or rest to move the cursor toward the target. Parts of somatosensory, temporal, and parietal areas exclusively had increased HBP when subjects were using motor imagery. In contrast, only part of the parietal cortex near the angular gyrus exclusively had an increase in HBP during rest. This investigation is, to our knowledge, the first to explore cortical fields changes in the context of continuous control in ECoG BCI. We present topographical changes in HBP characteristic specific to the generation of error. By focusing on continuous control, instead of on discrete control for simple selection, we investigate a more naturalistic setting and provide high ecological validity for characterizing error potentials. Such potentials could be considered as design elements for co-adaptive BCIs in the future as task-independent feedback to the decoder, allowing for more robust and individualized BCIs. |
format | Online Article Text |
id | pubmed-6541115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65411152019-06-12 Cortical Topography of Error-Related High-Frequency Potentials During Erroneous Control in a Continuous Control Brain–Computer Interface Wilson, Nile R. Sarma, Devapratim Wander, Jeremiah D. Weaver, Kurt E. Ojemann, Jeffrey G. Rao, Rajesh P. N. Front Neurosci Neuroscience Brain–computer interfaces (BCIs) benefit greatly from performance feedback, but current systems lack automatic, task-independent feedback. Cortical responses elicited from user error have the potential to serve as state-based feedback to BCI decoders. To gain a better understanding of local error potentials, we investigate responsive cortical power underlying error-related potentials (ErrPs) from the human cortex during a one-dimensional center-out BCI task, tracking the topography of high-gamma (70–100 Hz) band power (HBP) specific to BCI error. We measured electrocorticography (ECoG) in three human subjects during dynamic, continuous control over BCI cursor velocity. Subjects used motor imagery and rest to move the cursor toward and subsequently dwell within a target region. We then identified and labeled epochs where the BCI decoder incorrectly moved the cursor in the direction opposite of the subject’s expectations (i.e., BCI error). We found increased HBP in various cortical areas 100–500 ms following BCI error with respect to epochs of correct, intended control. Significant responses were noted in primary somatosensory, motor, premotor, and parietal areas and generally regardless of whether the subject was using motor imagery or rest to move the cursor toward the target. Parts of somatosensory, temporal, and parietal areas exclusively had increased HBP when subjects were using motor imagery. In contrast, only part of the parietal cortex near the angular gyrus exclusively had an increase in HBP during rest. This investigation is, to our knowledge, the first to explore cortical fields changes in the context of continuous control in ECoG BCI. We present topographical changes in HBP characteristic specific to the generation of error. By focusing on continuous control, instead of on discrete control for simple selection, we investigate a more naturalistic setting and provide high ecological validity for characterizing error potentials. Such potentials could be considered as design elements for co-adaptive BCIs in the future as task-independent feedback to the decoder, allowing for more robust and individualized BCIs. Frontiers Media S.A. 2019-05-22 /pmc/articles/PMC6541115/ /pubmed/31191218 http://dx.doi.org/10.3389/fnins.2019.00502 Text en Copyright © 2019 Wilson, Sarma, Wander, Weaver, Ojemann and Rao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Wilson, Nile R. Sarma, Devapratim Wander, Jeremiah D. Weaver, Kurt E. Ojemann, Jeffrey G. Rao, Rajesh P. N. Cortical Topography of Error-Related High-Frequency Potentials During Erroneous Control in a Continuous Control Brain–Computer Interface |
title | Cortical Topography of Error-Related High-Frequency Potentials During Erroneous Control in a Continuous Control Brain–Computer Interface |
title_full | Cortical Topography of Error-Related High-Frequency Potentials During Erroneous Control in a Continuous Control Brain–Computer Interface |
title_fullStr | Cortical Topography of Error-Related High-Frequency Potentials During Erroneous Control in a Continuous Control Brain–Computer Interface |
title_full_unstemmed | Cortical Topography of Error-Related High-Frequency Potentials During Erroneous Control in a Continuous Control Brain–Computer Interface |
title_short | Cortical Topography of Error-Related High-Frequency Potentials During Erroneous Control in a Continuous Control Brain–Computer Interface |
title_sort | cortical topography of error-related high-frequency potentials during erroneous control in a continuous control brain–computer interface |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541115/ https://www.ncbi.nlm.nih.gov/pubmed/31191218 http://dx.doi.org/10.3389/fnins.2019.00502 |
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