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Single-trial ERP Quantification Using Neural Networks

Traditional approaches to quantify components in event-related potentials (ERPs) are based on averaging EEG responses. However, this method ignores the trial-to-trial variability in the component’s latency, resulting in a smeared version of the component and underestimates of its amplitude. Differen...

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Autores principales: Depuydt, Emma, Criel, Yana, De Letter, Miet, van Mierlo, Pieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522773/
https://www.ncbi.nlm.nih.gov/pubmed/37552434
http://dx.doi.org/10.1007/s10548-023-00991-8
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author Depuydt, Emma
Criel, Yana
De Letter, Miet
van Mierlo, Pieter
author_facet Depuydt, Emma
Criel, Yana
De Letter, Miet
van Mierlo, Pieter
author_sort Depuydt, Emma
collection PubMed
description Traditional approaches to quantify components in event-related potentials (ERPs) are based on averaging EEG responses. However, this method ignores the trial-to-trial variability in the component’s latency, resulting in a smeared version of the component and underestimates of its amplitude. Different techniques to quantify ERP components in single trials have therefore been described in literature. In this study, two approaches based on neural networks are proposed and their performance was compared with other techniques using simulated data and two experimental datasets. On the simulated dataset, the neural networks outperformed other techniques for most signal-to-noise ratios and resulted in better estimates of the topography and shape of the ERP component. In the first experimental dataset, the highest correlation values between the estimated latencies of the P300 component and the reaction times were obtained using the neural networks. In the second dataset, the single-trial latency estimation techniques showed an amplitude reduction of the N400 effect with age and ascertained this effect could not be attributed to differences in latency variability. These results illustrate the applicability and the added value of neural networks for the quantification of ERP components in individual trials. A limitation, however, is that simulated data is needed to train the neural networks, which can be difficult when the ERP components to be found are not known a priori. Nevertheless, the neural networks-based approaches offer more information on the variability of the timing of the component and result in better estimates of the shape and topography of ERP components.
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spelling pubmed-105227732023-09-28 Single-trial ERP Quantification Using Neural Networks Depuydt, Emma Criel, Yana De Letter, Miet van Mierlo, Pieter Brain Topogr Original Paper Traditional approaches to quantify components in event-related potentials (ERPs) are based on averaging EEG responses. However, this method ignores the trial-to-trial variability in the component’s latency, resulting in a smeared version of the component and underestimates of its amplitude. Different techniques to quantify ERP components in single trials have therefore been described in literature. In this study, two approaches based on neural networks are proposed and their performance was compared with other techniques using simulated data and two experimental datasets. On the simulated dataset, the neural networks outperformed other techniques for most signal-to-noise ratios and resulted in better estimates of the topography and shape of the ERP component. In the first experimental dataset, the highest correlation values between the estimated latencies of the P300 component and the reaction times were obtained using the neural networks. In the second dataset, the single-trial latency estimation techniques showed an amplitude reduction of the N400 effect with age and ascertained this effect could not be attributed to differences in latency variability. These results illustrate the applicability and the added value of neural networks for the quantification of ERP components in individual trials. A limitation, however, is that simulated data is needed to train the neural networks, which can be difficult when the ERP components to be found are not known a priori. Nevertheless, the neural networks-based approaches offer more information on the variability of the timing of the component and result in better estimates of the shape and topography of ERP components. Springer US 2023-08-08 2023 /pmc/articles/PMC10522773/ /pubmed/37552434 http://dx.doi.org/10.1007/s10548-023-00991-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Paper
Depuydt, Emma
Criel, Yana
De Letter, Miet
van Mierlo, Pieter
Single-trial ERP Quantification Using Neural Networks
title Single-trial ERP Quantification Using Neural Networks
title_full Single-trial ERP Quantification Using Neural Networks
title_fullStr Single-trial ERP Quantification Using Neural Networks
title_full_unstemmed Single-trial ERP Quantification Using Neural Networks
title_short Single-trial ERP Quantification Using Neural Networks
title_sort single-trial erp quantification using neural networks
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10522773/
https://www.ncbi.nlm.nih.gov/pubmed/37552434
http://dx.doi.org/10.1007/s10548-023-00991-8
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