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Multiplex Networks to Characterize Seizure Development in Traumatic Brain Injury Patients

Traumatic brain injury (TBI) may cause secondary debilitating problems, such as post-traumatic epilepsy (PTE), which occurs with unprovoked recurrent seizures, months or even years after TBI. Currently, the Epilepsy Bioinformatics Study for Antiepileptogenic Therapy (EpiBioS4Rx) has been enrolling m...

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Autores principales: La Rocca, Marianna, Garner, Rachael, Amoroso, Nicola, Lutkenhoff, Evan S., Monti, Martin M., Vespa, Paul, Toga, Arthur W., Duncan, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734183/
https://www.ncbi.nlm.nih.gov/pubmed/33328863
http://dx.doi.org/10.3389/fnins.2020.591662
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author La Rocca, Marianna
Garner, Rachael
Amoroso, Nicola
Lutkenhoff, Evan S.
Monti, Martin M.
Vespa, Paul
Toga, Arthur W.
Duncan, Dominique
author_facet La Rocca, Marianna
Garner, Rachael
Amoroso, Nicola
Lutkenhoff, Evan S.
Monti, Martin M.
Vespa, Paul
Toga, Arthur W.
Duncan, Dominique
author_sort La Rocca, Marianna
collection PubMed
description Traumatic brain injury (TBI) may cause secondary debilitating problems, such as post-traumatic epilepsy (PTE), which occurs with unprovoked recurrent seizures, months or even years after TBI. Currently, the Epilepsy Bioinformatics Study for Antiepileptogenic Therapy (EpiBioS4Rx) has been enrolling moderate-severe TBI patients with the goal to identify biomarkers of epileptogenesis that may help to prevent seizure occurrence and better understand the mechanism underlying PTE. In this work, we used a novel complex network approach based on segmenting T1-weighted Magnetic Resonance Imaging (MRI) scans in patches of the same dimension (network nodes) and measured pairwise patch similarities using Pearson's correlation (network connections). This network model allowed us to obtain a series of single and multiplex network metrics to comprehensively analyze the different interactions between brain components and capture structural MRI alterations related to seizure development. We used these complex network features to train a Random Forest (RF) classifier and predict, with an accuracy of 70 and a 95% confidence interval of [67, 73%], which subjects from EpiBioS4Rx have had at least one seizure after a TBI. This complex network approach also allowed the identification of the most informative scales and brain areas for the discrimination between the two clinical groups: seizure-free and seizure-affected subjects, demonstrating to be a promising pilot study which, in the future, may serve to identify and validate biomarkers of PTE.
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spelling pubmed-77341832020-12-15 Multiplex Networks to Characterize Seizure Development in Traumatic Brain Injury Patients La Rocca, Marianna Garner, Rachael Amoroso, Nicola Lutkenhoff, Evan S. Monti, Martin M. Vespa, Paul Toga, Arthur W. Duncan, Dominique Front Neurosci Neuroscience Traumatic brain injury (TBI) may cause secondary debilitating problems, such as post-traumatic epilepsy (PTE), which occurs with unprovoked recurrent seizures, months or even years after TBI. Currently, the Epilepsy Bioinformatics Study for Antiepileptogenic Therapy (EpiBioS4Rx) has been enrolling moderate-severe TBI patients with the goal to identify biomarkers of epileptogenesis that may help to prevent seizure occurrence and better understand the mechanism underlying PTE. In this work, we used a novel complex network approach based on segmenting T1-weighted Magnetic Resonance Imaging (MRI) scans in patches of the same dimension (network nodes) and measured pairwise patch similarities using Pearson's correlation (network connections). This network model allowed us to obtain a series of single and multiplex network metrics to comprehensively analyze the different interactions between brain components and capture structural MRI alterations related to seizure development. We used these complex network features to train a Random Forest (RF) classifier and predict, with an accuracy of 70 and a 95% confidence interval of [67, 73%], which subjects from EpiBioS4Rx have had at least one seizure after a TBI. This complex network approach also allowed the identification of the most informative scales and brain areas for the discrimination between the two clinical groups: seizure-free and seizure-affected subjects, demonstrating to be a promising pilot study which, in the future, may serve to identify and validate biomarkers of PTE. Frontiers Media S.A. 2020-11-30 /pmc/articles/PMC7734183/ /pubmed/33328863 http://dx.doi.org/10.3389/fnins.2020.591662 Text en Copyright © 2020 La Rocca, Garner, Amoroso, Lutkenhoff, Monti, Vespa, Toga and Duncan. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
La Rocca, Marianna
Garner, Rachael
Amoroso, Nicola
Lutkenhoff, Evan S.
Monti, Martin M.
Vespa, Paul
Toga, Arthur W.
Duncan, Dominique
Multiplex Networks to Characterize Seizure Development in Traumatic Brain Injury Patients
title Multiplex Networks to Characterize Seizure Development in Traumatic Brain Injury Patients
title_full Multiplex Networks to Characterize Seizure Development in Traumatic Brain Injury Patients
title_fullStr Multiplex Networks to Characterize Seizure Development in Traumatic Brain Injury Patients
title_full_unstemmed Multiplex Networks to Characterize Seizure Development in Traumatic Brain Injury Patients
title_short Multiplex Networks to Characterize Seizure Development in Traumatic Brain Injury Patients
title_sort multiplex networks to characterize seizure development in traumatic brain injury patients
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734183/
https://www.ncbi.nlm.nih.gov/pubmed/33328863
http://dx.doi.org/10.3389/fnins.2020.591662
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