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author Trebaul, Lena
Deman, Pierre
Tuyisenge, Viateur
Jedynak, Maciej
Hugues, Etienne
Rudrauf, David
Bhattacharjee, Manik
Tadel, François
Chanteloup-Foret, Blandine
Saubat, Carole
Reyes Mejia, Gina Catalina
Adam, Claude
Nica, Anca
Pail, Martin
Dubeau, François
Rheims, Sylvain
Trébuchon, Agnès
Wang, Haixiang
Liu, Sinclair
Blauwblomme, Thomas
Garcés, Mercedes
De Palma, Luca
Valentin, Antonio
Metsähonkala, Eeva-Liisa
Petrescu, Ana Maria
Landré, Elizabeth
Szurhaj, William
Hirsch, Edouard
Valton, Luc
Rocamora, Rodrigo
Schulze-Bonhage, Andreas
Mindruta, Ioana
Francione, Stefano
Maillard, Louis
Taussig, Delphine
Kahane, Philippe
David, Olivier
author_facet Trebaul, Lena
Deman, Pierre
Tuyisenge, Viateur
Jedynak, Maciej
Hugues, Etienne
Rudrauf, David
Bhattacharjee, Manik
Tadel, François
Chanteloup-Foret, Blandine
Saubat, Carole
Reyes Mejia, Gina Catalina
Adam, Claude
Nica, Anca
Pail, Martin
Dubeau, François
Rheims, Sylvain
Trébuchon, Agnès
Wang, Haixiang
Liu, Sinclair
Blauwblomme, Thomas
Garcés, Mercedes
De Palma, Luca
Valentin, Antonio
Metsähonkala, Eeva-Liisa
Petrescu, Ana Maria
Landré, Elizabeth
Szurhaj, William
Hirsch, Edouard
Valton, Luc
Rocamora, Rodrigo
Schulze-Bonhage, Andreas
Mindruta, Ioana
Francione, Stefano
Maillard, Louis
Taussig, Delphine
Kahane, Philippe
David, Olivier
author_sort Trebaul, Lena
collection PubMed
description In patients with pharmaco-resistant focal epilepsies investigated with intracranial electroencephalography (iEEG), direct electrical stimulations of a cortical region induce cortico-cortical evoked potentials (CCEP) in distant cerebral cortex, which properties can be used to infer large scale brain connectivity. In 2013, we proposed a new probabilistic functional tractography methodology to study human brain connectivity. We have now been revisiting this method in the F-TRACT project (f-tract.eu) by developing a large multicenter CCEP database of several thousand stimulation runs performed in several hundred patients, and associated processing tools to create a probabilistic atlas of human cortico-cortical connections. Here, we wish to present a snapshot of the methods and data of F-TRACT using a pool of 213 epilepsy patients, all studied by stereo-encephalography with intracerebral depth electrodes. The CCEPs were processed using an automated pipeline with the following consecutive steps: detection of each stimulation run from stimulation artifacts in raw intracranial EEG (iEEG) files, bad channels detection with a machine learning approach, model-based stimulation artifact correction, robust averaging over stimulation pulses. Effective connectivity between the stimulated and recording areas is then inferred from the properties of the first CCEP component, i.e. onset and peak latency, amplitude, duration and integral of the significant part. Finally, group statistics of CCEP features are implemented for each brain parcel explored by iEEG electrodes. The localization (coordinates, white/gray matter relative positioning) of electrode contacts were obtained from imaging data (anatomical MRI or CT scans before and after electrodes implantation). The iEEG contacts were repositioned in different brain parcellations from the segmentation of patients' anatomical MRI or from templates in the MNI coordinate system. The F-TRACT database using the first pool of 213 patients provided connectivity probability values for 95% of possible intrahemispheric and 56% of interhemispheric connections and CCEP features for 78% of intrahemisheric and 14% of interhemispheric connections. In this report, we show some examples of anatomo-functional connectivity matrices, and associated directional maps. We also indicate how CCEP features, especially latencies, are related to spatial distances, and allow estimating the velocity distribution of neuronal signals at a large scale. Finally, we describe the impact on the estimated connectivity of the stimulation charge and of the contact localization according to the white or gray matter. The most relevant maps for the scientific community are available for download on f-tract. eu (David et al., 2017) and will be regularly updated during the following months with the addition of more data in the F-TRACT database. This will provide an unprecedented knowledge on the dynamical properties of large fiber tracts in human.
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spelling pubmed-61509492018-11-01 Probabilistic functional tractography of the human cortex revisited Trebaul, Lena Deman, Pierre Tuyisenge, Viateur Jedynak, Maciej Hugues, Etienne Rudrauf, David Bhattacharjee, Manik Tadel, François Chanteloup-Foret, Blandine Saubat, Carole Reyes Mejia, Gina Catalina Adam, Claude Nica, Anca Pail, Martin Dubeau, François Rheims, Sylvain Trébuchon, Agnès Wang, Haixiang Liu, Sinclair Blauwblomme, Thomas Garcés, Mercedes De Palma, Luca Valentin, Antonio Metsähonkala, Eeva-Liisa Petrescu, Ana Maria Landré, Elizabeth Szurhaj, William Hirsch, Edouard Valton, Luc Rocamora, Rodrigo Schulze-Bonhage, Andreas Mindruta, Ioana Francione, Stefano Maillard, Louis Taussig, Delphine Kahane, Philippe David, Olivier Neuroimage Article In patients with pharmaco-resistant focal epilepsies investigated with intracranial electroencephalography (iEEG), direct electrical stimulations of a cortical region induce cortico-cortical evoked potentials (CCEP) in distant cerebral cortex, which properties can be used to infer large scale brain connectivity. In 2013, we proposed a new probabilistic functional tractography methodology to study human brain connectivity. We have now been revisiting this method in the F-TRACT project (f-tract.eu) by developing a large multicenter CCEP database of several thousand stimulation runs performed in several hundred patients, and associated processing tools to create a probabilistic atlas of human cortico-cortical connections. Here, we wish to present a snapshot of the methods and data of F-TRACT using a pool of 213 epilepsy patients, all studied by stereo-encephalography with intracerebral depth electrodes. The CCEPs were processed using an automated pipeline with the following consecutive steps: detection of each stimulation run from stimulation artifacts in raw intracranial EEG (iEEG) files, bad channels detection with a machine learning approach, model-based stimulation artifact correction, robust averaging over stimulation pulses. Effective connectivity between the stimulated and recording areas is then inferred from the properties of the first CCEP component, i.e. onset and peak latency, amplitude, duration and integral of the significant part. Finally, group statistics of CCEP features are implemented for each brain parcel explored by iEEG electrodes. The localization (coordinates, white/gray matter relative positioning) of electrode contacts were obtained from imaging data (anatomical MRI or CT scans before and after electrodes implantation). The iEEG contacts were repositioned in different brain parcellations from the segmentation of patients' anatomical MRI or from templates in the MNI coordinate system. The F-TRACT database using the first pool of 213 patients provided connectivity probability values for 95% of possible intrahemispheric and 56% of interhemispheric connections and CCEP features for 78% of intrahemisheric and 14% of interhemispheric connections. In this report, we show some examples of anatomo-functional connectivity matrices, and associated directional maps. We also indicate how CCEP features, especially latencies, are related to spatial distances, and allow estimating the velocity distribution of neuronal signals at a large scale. Finally, we describe the impact on the estimated connectivity of the stimulation charge and of the contact localization according to the white or gray matter. The most relevant maps for the scientific community are available for download on f-tract. eu (David et al., 2017) and will be regularly updated during the following months with the addition of more data in the F-TRACT database. This will provide an unprecedented knowledge on the dynamical properties of large fiber tracts in human. Academic Press 2018-11-01 /pmc/articles/PMC6150949/ /pubmed/30025851 http://dx.doi.org/10.1016/j.neuroimage.2018.07.039 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Trebaul, Lena
Deman, Pierre
Tuyisenge, Viateur
Jedynak, Maciej
Hugues, Etienne
Rudrauf, David
Bhattacharjee, Manik
Tadel, François
Chanteloup-Foret, Blandine
Saubat, Carole
Reyes Mejia, Gina Catalina
Adam, Claude
Nica, Anca
Pail, Martin
Dubeau, François
Rheims, Sylvain
Trébuchon, Agnès
Wang, Haixiang
Liu, Sinclair
Blauwblomme, Thomas
Garcés, Mercedes
De Palma, Luca
Valentin, Antonio
Metsähonkala, Eeva-Liisa
Petrescu, Ana Maria
Landré, Elizabeth
Szurhaj, William
Hirsch, Edouard
Valton, Luc
Rocamora, Rodrigo
Schulze-Bonhage, Andreas
Mindruta, Ioana
Francione, Stefano
Maillard, Louis
Taussig, Delphine
Kahane, Philippe
David, Olivier
Probabilistic functional tractography of the human cortex revisited
title Probabilistic functional tractography of the human cortex revisited
title_full Probabilistic functional tractography of the human cortex revisited
title_fullStr Probabilistic functional tractography of the human cortex revisited
title_full_unstemmed Probabilistic functional tractography of the human cortex revisited
title_short Probabilistic functional tractography of the human cortex revisited
title_sort probabilistic functional tractography of the human cortex revisited
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150949/
https://www.ncbi.nlm.nih.gov/pubmed/30025851
http://dx.doi.org/10.1016/j.neuroimage.2018.07.039
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