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Trial by trial EEG based BCI for distress versus non distress classification in individuals with ASD
Autism spectrum disorder (ASD) is a neurodevelopmental disorder that is often accompanied by impaired emotion regulation (ER). There has been increasing emphasis on developing evidence-based approaches to improve ER in ASD. Electroencephalography (EEG) has shown success in reducing ASD symptoms when...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971030/ https://www.ncbi.nlm.nih.gov/pubmed/33727625 http://dx.doi.org/10.1038/s41598-021-85362-8 |
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author | Eldeeb, Safaa Susam, Busra T. Akcakaya, Murat Conner, Caitlin M. White, Susan W. Mazefsky, Carla A. |
author_facet | Eldeeb, Safaa Susam, Busra T. Akcakaya, Murat Conner, Caitlin M. White, Susan W. Mazefsky, Carla A. |
author_sort | Eldeeb, Safaa |
collection | PubMed |
description | Autism spectrum disorder (ASD) is a neurodevelopmental disorder that is often accompanied by impaired emotion regulation (ER). There has been increasing emphasis on developing evidence-based approaches to improve ER in ASD. Electroencephalography (EEG) has shown success in reducing ASD symptoms when used in neurofeedback-based interventions. Also, certain EEG components are associated with ER. Our overarching goal is to develop a technology that will use EEG to monitor real-time changes in ER and perform intervention based on these changes. As a first step, an EEG-based brain computer interface that is based on an Affective Posner task was developed to identify patterns associated with ER on a single trial basis, and EEG data collected from 21 individuals with ASD. Accordingly, our aim in this study is to investigate EEG features that could differentiate between distress and non-distress conditions. Specifically, we investigate if the EEG time-locked to the visual feedback presentation could be used to classify between WIN (non-distress) and LOSE (distress) conditions in a game with deception. Results showed that the extracted EEG features could differentiate between WIN and LOSE conditions (average accuracy of 81%), LOSE and rest-EEG conditions (average accuracy 94.8%), and WIN and rest-EEG conditions (average accuracy 94.9%). |
format | Online Article Text |
id | pubmed-7971030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79710302021-03-19 Trial by trial EEG based BCI for distress versus non distress classification in individuals with ASD Eldeeb, Safaa Susam, Busra T. Akcakaya, Murat Conner, Caitlin M. White, Susan W. Mazefsky, Carla A. Sci Rep Article Autism spectrum disorder (ASD) is a neurodevelopmental disorder that is often accompanied by impaired emotion regulation (ER). There has been increasing emphasis on developing evidence-based approaches to improve ER in ASD. Electroencephalography (EEG) has shown success in reducing ASD symptoms when used in neurofeedback-based interventions. Also, certain EEG components are associated with ER. Our overarching goal is to develop a technology that will use EEG to monitor real-time changes in ER and perform intervention based on these changes. As a first step, an EEG-based brain computer interface that is based on an Affective Posner task was developed to identify patterns associated with ER on a single trial basis, and EEG data collected from 21 individuals with ASD. Accordingly, our aim in this study is to investigate EEG features that could differentiate between distress and non-distress conditions. Specifically, we investigate if the EEG time-locked to the visual feedback presentation could be used to classify between WIN (non-distress) and LOSE (distress) conditions in a game with deception. Results showed that the extracted EEG features could differentiate between WIN and LOSE conditions (average accuracy of 81%), LOSE and rest-EEG conditions (average accuracy 94.8%), and WIN and rest-EEG conditions (average accuracy 94.9%). Nature Publishing Group UK 2021-03-16 /pmc/articles/PMC7971030/ /pubmed/33727625 http://dx.doi.org/10.1038/s41598-021-85362-8 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Eldeeb, Safaa Susam, Busra T. Akcakaya, Murat Conner, Caitlin M. White, Susan W. Mazefsky, Carla A. Trial by trial EEG based BCI for distress versus non distress classification in individuals with ASD |
title | Trial by trial EEG based BCI for distress versus non distress classification in individuals with ASD |
title_full | Trial by trial EEG based BCI for distress versus non distress classification in individuals with ASD |
title_fullStr | Trial by trial EEG based BCI for distress versus non distress classification in individuals with ASD |
title_full_unstemmed | Trial by trial EEG based BCI for distress versus non distress classification in individuals with ASD |
title_short | Trial by trial EEG based BCI for distress versus non distress classification in individuals with ASD |
title_sort | trial by trial eeg based bci for distress versus non distress classification in individuals with asd |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7971030/ https://www.ncbi.nlm.nih.gov/pubmed/33727625 http://dx.doi.org/10.1038/s41598-021-85362-8 |
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