Cargando…
Structure predicts function: Combining non-invasive electrophysiology with in-vivo histology
We present an approach for combining high resolution MRI-based myelin mapping with functional information from electroencephalography (EEG) or magnetoencephalography (MEG). The main contribution to the primary currents detectable with EEG and MEG comes from ionic currents in the apical dendrites of...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334663/ https://www.ncbi.nlm.nih.gov/pubmed/25529007 http://dx.doi.org/10.1016/j.neuroimage.2014.12.030 |
_version_ | 1782358227340492800 |
---|---|
author | Helbling, Saskia Teki, Sundeep Callaghan, Martina F. Sedley, William Mohammadi, Siawoosh Griffiths, Timothy D. Weiskopf, Nikolaus Barnes, Gareth R. |
author_facet | Helbling, Saskia Teki, Sundeep Callaghan, Martina F. Sedley, William Mohammadi, Siawoosh Griffiths, Timothy D. Weiskopf, Nikolaus Barnes, Gareth R. |
author_sort | Helbling, Saskia |
collection | PubMed |
description | We present an approach for combining high resolution MRI-based myelin mapping with functional information from electroencephalography (EEG) or magnetoencephalography (MEG). The main contribution to the primary currents detectable with EEG and MEG comes from ionic currents in the apical dendrites of cortical pyramidal cells, aligned perpendicularly to the local cortical surface. We provide evidence from an in-vivo experiment that the variation in MRI-based myeloarchitecture measures across the cortex predicts the variation of the current density over individuals and thus is of functional relevance. Equivalent current dipole locations and moments due to pitch onset evoked response fields (ERFs) were estimated by means of a variational Bayesian algorithm. The myeloarchitecture was estimated indirectly from individual high resolution quantitative multi-parameter maps (MPMs) acquired at 800 μm isotropic resolution. Myelin estimates across cortical areas correlated positively with dipole magnitude. This correlation was spatially specific: regions of interest in the auditory cortex provided significantly better models than those covering whole hemispheres. Based on the MPM data we identified the auditory cortical area TE1.2 as the most likely origin of the pitch ERFs measured by MEG. We can now proceed to exploit the higher spatial resolution of quantitative MPMs to identify the cortical origin of M/EEG signals, inform M/EEG source reconstruction and explore structure–function relationships at a fine structural level in the living human brain. |
format | Online Article Text |
id | pubmed-4334663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43346632015-03-03 Structure predicts function: Combining non-invasive electrophysiology with in-vivo histology Helbling, Saskia Teki, Sundeep Callaghan, Martina F. Sedley, William Mohammadi, Siawoosh Griffiths, Timothy D. Weiskopf, Nikolaus Barnes, Gareth R. Neuroimage Article We present an approach for combining high resolution MRI-based myelin mapping with functional information from electroencephalography (EEG) or magnetoencephalography (MEG). The main contribution to the primary currents detectable with EEG and MEG comes from ionic currents in the apical dendrites of cortical pyramidal cells, aligned perpendicularly to the local cortical surface. We provide evidence from an in-vivo experiment that the variation in MRI-based myeloarchitecture measures across the cortex predicts the variation of the current density over individuals and thus is of functional relevance. Equivalent current dipole locations and moments due to pitch onset evoked response fields (ERFs) were estimated by means of a variational Bayesian algorithm. The myeloarchitecture was estimated indirectly from individual high resolution quantitative multi-parameter maps (MPMs) acquired at 800 μm isotropic resolution. Myelin estimates across cortical areas correlated positively with dipole magnitude. This correlation was spatially specific: regions of interest in the auditory cortex provided significantly better models than those covering whole hemispheres. Based on the MPM data we identified the auditory cortical area TE1.2 as the most likely origin of the pitch ERFs measured by MEG. We can now proceed to exploit the higher spatial resolution of quantitative MPMs to identify the cortical origin of M/EEG signals, inform M/EEG source reconstruction and explore structure–function relationships at a fine structural level in the living human brain. Academic Press 2015-03 /pmc/articles/PMC4334663/ /pubmed/25529007 http://dx.doi.org/10.1016/j.neuroimage.2014.12.030 Text en © 2014 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Helbling, Saskia Teki, Sundeep Callaghan, Martina F. Sedley, William Mohammadi, Siawoosh Griffiths, Timothy D. Weiskopf, Nikolaus Barnes, Gareth R. Structure predicts function: Combining non-invasive electrophysiology with in-vivo histology |
title | Structure predicts function: Combining non-invasive electrophysiology with in-vivo histology |
title_full | Structure predicts function: Combining non-invasive electrophysiology with in-vivo histology |
title_fullStr | Structure predicts function: Combining non-invasive electrophysiology with in-vivo histology |
title_full_unstemmed | Structure predicts function: Combining non-invasive electrophysiology with in-vivo histology |
title_short | Structure predicts function: Combining non-invasive electrophysiology with in-vivo histology |
title_sort | structure predicts function: combining non-invasive electrophysiology with in-vivo histology |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4334663/ https://www.ncbi.nlm.nih.gov/pubmed/25529007 http://dx.doi.org/10.1016/j.neuroimage.2014.12.030 |
work_keys_str_mv | AT helblingsaskia structurepredictsfunctioncombiningnoninvasiveelectrophysiologywithinvivohistology AT tekisundeep structurepredictsfunctioncombiningnoninvasiveelectrophysiologywithinvivohistology AT callaghanmartinaf structurepredictsfunctioncombiningnoninvasiveelectrophysiologywithinvivohistology AT sedleywilliam structurepredictsfunctioncombiningnoninvasiveelectrophysiologywithinvivohistology AT mohammadisiawoosh structurepredictsfunctioncombiningnoninvasiveelectrophysiologywithinvivohistology AT griffithstimothyd structurepredictsfunctioncombiningnoninvasiveelectrophysiologywithinvivohistology AT weiskopfnikolaus structurepredictsfunctioncombiningnoninvasiveelectrophysiologywithinvivohistology AT barnesgarethr structurepredictsfunctioncombiningnoninvasiveelectrophysiologywithinvivohistology |