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Decoding Sequence Learning from Single-Trial Intracranial EEG in Humans
We propose and validate a multivariate classification algorithm for characterizing changes in human intracranial electroencephalographic data (iEEG) after learning motor sequences. The algorithm is based on a Hidden Markov Model (HMM) that captures spatio-temporal properties of the iEEG at the level...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235148/ https://www.ncbi.nlm.nih.gov/pubmed/22174850 http://dx.doi.org/10.1371/journal.pone.0028630 |
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author | De Lucia, Marzia Constantinescu, Irina Sterpenich, Virginie Pourtois, Gilles Seeck, Margitta Schwartz, Sophie |
author_facet | De Lucia, Marzia Constantinescu, Irina Sterpenich, Virginie Pourtois, Gilles Seeck, Margitta Schwartz, Sophie |
author_sort | De Lucia, Marzia |
collection | PubMed |
description | We propose and validate a multivariate classification algorithm for characterizing changes in human intracranial electroencephalographic data (iEEG) after learning motor sequences. The algorithm is based on a Hidden Markov Model (HMM) that captures spatio-temporal properties of the iEEG at the level of single trials. Continuous intracranial iEEG was acquired during two sessions (one before and one after a night of sleep) in two patients with depth electrodes implanted in several brain areas. They performed a visuomotor sequence (serial reaction time task, SRTT) using the fingers of their non-dominant hand. Our results show that the decoding algorithm correctly classified single iEEG trials from the trained sequence as belonging to either the initial training phase (day 1, before sleep) or a later consolidated phase (day 2, after sleep), whereas it failed to do so for trials belonging to a control condition (pseudo-random sequence). Accurate single-trial classification was achieved by taking advantage of the distributed pattern of neural activity. However, across all the contacts the hippocampus contributed most significantly to the classification accuracy for both patients, and one fronto-striatal contact for one patient. Together, these human intracranial findings demonstrate that a multivariate decoding approach can detect learning-related changes at the level of single-trial iEEG. Because it allows an unbiased identification of brain sites contributing to a behavioral effect (or experimental condition) at the level of single subject, this approach could be usefully applied to assess the neural correlates of other complex cognitive functions in patients implanted with multiple electrodes. |
format | Online Article Text |
id | pubmed-3235148 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32351482011-12-15 Decoding Sequence Learning from Single-Trial Intracranial EEG in Humans De Lucia, Marzia Constantinescu, Irina Sterpenich, Virginie Pourtois, Gilles Seeck, Margitta Schwartz, Sophie PLoS One Research Article We propose and validate a multivariate classification algorithm for characterizing changes in human intracranial electroencephalographic data (iEEG) after learning motor sequences. The algorithm is based on a Hidden Markov Model (HMM) that captures spatio-temporal properties of the iEEG at the level of single trials. Continuous intracranial iEEG was acquired during two sessions (one before and one after a night of sleep) in two patients with depth electrodes implanted in several brain areas. They performed a visuomotor sequence (serial reaction time task, SRTT) using the fingers of their non-dominant hand. Our results show that the decoding algorithm correctly classified single iEEG trials from the trained sequence as belonging to either the initial training phase (day 1, before sleep) or a later consolidated phase (day 2, after sleep), whereas it failed to do so for trials belonging to a control condition (pseudo-random sequence). Accurate single-trial classification was achieved by taking advantage of the distributed pattern of neural activity. However, across all the contacts the hippocampus contributed most significantly to the classification accuracy for both patients, and one fronto-striatal contact for one patient. Together, these human intracranial findings demonstrate that a multivariate decoding approach can detect learning-related changes at the level of single-trial iEEG. Because it allows an unbiased identification of brain sites contributing to a behavioral effect (or experimental condition) at the level of single subject, this approach could be usefully applied to assess the neural correlates of other complex cognitive functions in patients implanted with multiple electrodes. Public Library of Science 2011-12-09 /pmc/articles/PMC3235148/ /pubmed/22174850 http://dx.doi.org/10.1371/journal.pone.0028630 Text en De Lucia et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article De Lucia, Marzia Constantinescu, Irina Sterpenich, Virginie Pourtois, Gilles Seeck, Margitta Schwartz, Sophie Decoding Sequence Learning from Single-Trial Intracranial EEG in Humans |
title | Decoding Sequence Learning from Single-Trial Intracranial EEG in Humans |
title_full | Decoding Sequence Learning from Single-Trial Intracranial EEG in Humans |
title_fullStr | Decoding Sequence Learning from Single-Trial Intracranial EEG in Humans |
title_full_unstemmed | Decoding Sequence Learning from Single-Trial Intracranial EEG in Humans |
title_short | Decoding Sequence Learning from Single-Trial Intracranial EEG in Humans |
title_sort | decoding sequence learning from single-trial intracranial eeg in humans |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3235148/ https://www.ncbi.nlm.nih.gov/pubmed/22174850 http://dx.doi.org/10.1371/journal.pone.0028630 |
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