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Maximum-likelihood estimation of channel-dependent trial-to-trial variability of auditory evoked brain responses in MEG

BACKGROUND: We propose a mathematical model for multichannel assessment of the trial-to-trial variability of auditory evoked brain responses in magnetoencephalography (MEG). METHODS: Following the work of de Munck et al., our approach is based on the maximum likelihood estimation and involves an app...

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Autores principales: SieluŻycki, Cezary, Kordowski, Paweł
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060856/
https://www.ncbi.nlm.nih.gov/pubmed/24939398
http://dx.doi.org/10.1186/1475-925X-13-75
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author SieluŻycki, Cezary
Kordowski, Paweł
author_facet SieluŻycki, Cezary
Kordowski, Paweł
author_sort SieluŻycki, Cezary
collection PubMed
description BACKGROUND: We propose a mathematical model for multichannel assessment of the trial-to-trial variability of auditory evoked brain responses in magnetoencephalography (MEG). METHODS: Following the work of de Munck et al., our approach is based on the maximum likelihood estimation and involves an approximation of the spatio-temporal covariance of the contaminating background noise by means of the Kronecker product of its spatial and temporal covariance matrices. Extending the work of de Munck et al., where the trial-to-trial variability of the responses was considered identical to all channels, we evaluate it for each individual channel. RESULTS: Simulations with two equivalent current dipoles (ECDs) with different trial-to-trial variability, one seeded in each of the auditory cortices, were used to study the applicability of the proposed methodology on the sensor level and revealed spatial selectivity of the trial-to-trial estimates. In addition, we simulated a scenario with neighboring ECDs, to show limitations of the method. We also present an illustrative example of the application of this methodology to real MEG data taken from an auditory experimental paradigm, where we found hemispheric lateralization of the habituation effect to multiple stimulus presentation. CONCLUSIONS: The proposed algorithm is capable of reconstructing lateralization effects of the trial-to-trial variability of evoked responses, i.e. when an ECD of only one hemisphere habituates, whereas the activity of the other hemisphere is not subject to habituation. Hence, it may be a useful tool in paradigms that assume lateralization effects, like, e.g., those involving language processing.
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spelling pubmed-40608562014-06-30 Maximum-likelihood estimation of channel-dependent trial-to-trial variability of auditory evoked brain responses in MEG SieluŻycki, Cezary Kordowski, Paweł Biomed Eng Online Research BACKGROUND: We propose a mathematical model for multichannel assessment of the trial-to-trial variability of auditory evoked brain responses in magnetoencephalography (MEG). METHODS: Following the work of de Munck et al., our approach is based on the maximum likelihood estimation and involves an approximation of the spatio-temporal covariance of the contaminating background noise by means of the Kronecker product of its spatial and temporal covariance matrices. Extending the work of de Munck et al., where the trial-to-trial variability of the responses was considered identical to all channels, we evaluate it for each individual channel. RESULTS: Simulations with two equivalent current dipoles (ECDs) with different trial-to-trial variability, one seeded in each of the auditory cortices, were used to study the applicability of the proposed methodology on the sensor level and revealed spatial selectivity of the trial-to-trial estimates. In addition, we simulated a scenario with neighboring ECDs, to show limitations of the method. We also present an illustrative example of the application of this methodology to real MEG data taken from an auditory experimental paradigm, where we found hemispheric lateralization of the habituation effect to multiple stimulus presentation. CONCLUSIONS: The proposed algorithm is capable of reconstructing lateralization effects of the trial-to-trial variability of evoked responses, i.e. when an ECD of only one hemisphere habituates, whereas the activity of the other hemisphere is not subject to habituation. Hence, it may be a useful tool in paradigms that assume lateralization effects, like, e.g., those involving language processing. BioMed Central 2014-06-16 /pmc/articles/PMC4060856/ /pubmed/24939398 http://dx.doi.org/10.1186/1475-925X-13-75 Text en Copyright © 2014 SieluŻycki and Kordowski; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
SieluŻycki, Cezary
Kordowski, Paweł
Maximum-likelihood estimation of channel-dependent trial-to-trial variability of auditory evoked brain responses in MEG
title Maximum-likelihood estimation of channel-dependent trial-to-trial variability of auditory evoked brain responses in MEG
title_full Maximum-likelihood estimation of channel-dependent trial-to-trial variability of auditory evoked brain responses in MEG
title_fullStr Maximum-likelihood estimation of channel-dependent trial-to-trial variability of auditory evoked brain responses in MEG
title_full_unstemmed Maximum-likelihood estimation of channel-dependent trial-to-trial variability of auditory evoked brain responses in MEG
title_short Maximum-likelihood estimation of channel-dependent trial-to-trial variability of auditory evoked brain responses in MEG
title_sort maximum-likelihood estimation of channel-dependent trial-to-trial variability of auditory evoked brain responses in meg
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060856/
https://www.ncbi.nlm.nih.gov/pubmed/24939398
http://dx.doi.org/10.1186/1475-925X-13-75
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