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Retinotopic mapping of the primary visual cortex – a challenge for MEG imaging of the human cortex

Magnetoencephalography (MEG) can be used to reconstruct neuronal activity with high spatial and temporal resolution. However, this reconstruction problem is ill-posed, and requires the use of prior constraints in order to produce a unique solution. At present there are a multitude of inversion algor...

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Autores principales: Perry, Gavin, Adjamian, Peyman, Thai, Ngoc J, Holliday, Ian E, Hillebrand, Arjan, Barnes, Gareth R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178797/
https://www.ncbi.nlm.nih.gov/pubmed/21749494
http://dx.doi.org/10.1111/j.1460-9568.2011.07777.x
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author Perry, Gavin
Adjamian, Peyman
Thai, Ngoc J
Holliday, Ian E
Hillebrand, Arjan
Barnes, Gareth R
author_facet Perry, Gavin
Adjamian, Peyman
Thai, Ngoc J
Holliday, Ian E
Hillebrand, Arjan
Barnes, Gareth R
author_sort Perry, Gavin
collection PubMed
description Magnetoencephalography (MEG) can be used to reconstruct neuronal activity with high spatial and temporal resolution. However, this reconstruction problem is ill-posed, and requires the use of prior constraints in order to produce a unique solution. At present there are a multitude of inversion algorithms, each employing different assumptions, but one major problem when comparing the accuracy of these different approaches is that often the true underlying electrical state of the brain is unknown. In this study, we explore one paradigm, retinotopic mapping in the primary visual cortex (V1), for which the ground truth is known to a reasonable degree of accuracy, enabling the comparison of MEG source reconstructions with the true electrical state of the brain. Specifically, we attempted to localize, using a beanforming method, the induced responses in the visual cortex generated by a high contrast, retinotopically varying stimulus. Although well described in primate studies, it has been an open question whether the induced gamma power in humans due to high contrast gratings derives from V1 rather than the prestriate cortex (V2). We show that the beanformer source estimate in the gamma and theta bands does vary in a manner consistent with the known retinotopy of V1. However, these peak locations, although retinotopically organized, did not accurately localize to the cortical surface. We considered possible causes for this discrepancy and suggest that improved MEG/magnetic resonance imaging co-registration and the use of more accurate source models that take into account the spatial extent and shape of the active cortex may, in future, improve the accuracy of the source reconstructions.
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spelling pubmed-31787972011-09-28 Retinotopic mapping of the primary visual cortex – a challenge for MEG imaging of the human cortex Perry, Gavin Adjamian, Peyman Thai, Ngoc J Holliday, Ian E Hillebrand, Arjan Barnes, Gareth R Eur J Neurosci Cognitive Neuroscience Magnetoencephalography (MEG) can be used to reconstruct neuronal activity with high spatial and temporal resolution. However, this reconstruction problem is ill-posed, and requires the use of prior constraints in order to produce a unique solution. At present there are a multitude of inversion algorithms, each employing different assumptions, but one major problem when comparing the accuracy of these different approaches is that often the true underlying electrical state of the brain is unknown. In this study, we explore one paradigm, retinotopic mapping in the primary visual cortex (V1), for which the ground truth is known to a reasonable degree of accuracy, enabling the comparison of MEG source reconstructions with the true electrical state of the brain. Specifically, we attempted to localize, using a beanforming method, the induced responses in the visual cortex generated by a high contrast, retinotopically varying stimulus. Although well described in primate studies, it has been an open question whether the induced gamma power in humans due to high contrast gratings derives from V1 rather than the prestriate cortex (V2). We show that the beanformer source estimate in the gamma and theta bands does vary in a manner consistent with the known retinotopy of V1. However, these peak locations, although retinotopically organized, did not accurately localize to the cortical surface. We considered possible causes for this discrepancy and suggest that improved MEG/magnetic resonance imaging co-registration and the use of more accurate source models that take into account the spatial extent and shape of the active cortex may, in future, improve the accuracy of the source reconstructions. Blackwell Publishing Ltd 2011-08 /pmc/articles/PMC3178797/ /pubmed/21749494 http://dx.doi.org/10.1111/j.1460-9568.2011.07777.x Text en European Journal of Neuroscience © 2011 Federation of European Neuroscience Societies and Blackwell Publishing Ltd http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Cognitive Neuroscience
Perry, Gavin
Adjamian, Peyman
Thai, Ngoc J
Holliday, Ian E
Hillebrand, Arjan
Barnes, Gareth R
Retinotopic mapping of the primary visual cortex – a challenge for MEG imaging of the human cortex
title Retinotopic mapping of the primary visual cortex – a challenge for MEG imaging of the human cortex
title_full Retinotopic mapping of the primary visual cortex – a challenge for MEG imaging of the human cortex
title_fullStr Retinotopic mapping of the primary visual cortex – a challenge for MEG imaging of the human cortex
title_full_unstemmed Retinotopic mapping of the primary visual cortex – a challenge for MEG imaging of the human cortex
title_short Retinotopic mapping of the primary visual cortex – a challenge for MEG imaging of the human cortex
title_sort retinotopic mapping of the primary visual cortex – a challenge for meg imaging of the human cortex
topic Cognitive Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178797/
https://www.ncbi.nlm.nih.gov/pubmed/21749494
http://dx.doi.org/10.1111/j.1460-9568.2011.07777.x
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