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Deep learning distinguishes connectomes from focal epilepsy patients and controls: feasibility and clinical implications
The application of deep learning models to evaluate connectome data is gaining interest in epilepsy research. Deep learning may be a useful initial tool to partition connectome data into network subsets for further analysis. Few prior works have used deep learning to examine structural connectomes f...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644981/ https://www.ncbi.nlm.nih.gov/pubmed/38025275 http://dx.doi.org/10.1093/braincomms/fcad294 |
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author | Maher, Christina Tang, Zihao D’Souza, Arkiev Cabezas, Mariano Cai, Weidong Barnett, Michael Kavehei, Omid Wang, Chenyu Nikpour, Armin |
author_facet | Maher, Christina Tang, Zihao D’Souza, Arkiev Cabezas, Mariano Cai, Weidong Barnett, Michael Kavehei, Omid Wang, Chenyu Nikpour, Armin |
author_sort | Maher, Christina |
collection | PubMed |
description | The application of deep learning models to evaluate connectome data is gaining interest in epilepsy research. Deep learning may be a useful initial tool to partition connectome data into network subsets for further analysis. Few prior works have used deep learning to examine structural connectomes from patients with focal epilepsy. We evaluated whether a deep learning model applied to whole-brain connectomes could classify 28 participants with focal epilepsy from 20 controls and identify nodal importance for each group. Participants with epilepsy were further grouped based on whether they had focal seizures that evolved into bilateral tonic-clonic seizures (17 with, 11 without). The trained neural network classified patients from controls with an accuracy of 72.92%, while the seizure subtype groups achieved a classification accuracy of 67.86%. In the patient subgroups, the nodes and edges deemed important for accurate classification were also clinically relevant, indicating the model’s interpretability. The current work expands the evidence for the potential of deep learning to extract relevant markers from clinical datasets. Our findings offer a rationale for further research interrogating structural connectomes to obtain features that can be biomarkers and aid the diagnosis of seizure subtypes. |
format | Online Article Text |
id | pubmed-10644981 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-106449812023-10-31 Deep learning distinguishes connectomes from focal epilepsy patients and controls: feasibility and clinical implications Maher, Christina Tang, Zihao D’Souza, Arkiev Cabezas, Mariano Cai, Weidong Barnett, Michael Kavehei, Omid Wang, Chenyu Nikpour, Armin Brain Commun Original Article The application of deep learning models to evaluate connectome data is gaining interest in epilepsy research. Deep learning may be a useful initial tool to partition connectome data into network subsets for further analysis. Few prior works have used deep learning to examine structural connectomes from patients with focal epilepsy. We evaluated whether a deep learning model applied to whole-brain connectomes could classify 28 participants with focal epilepsy from 20 controls and identify nodal importance for each group. Participants with epilepsy were further grouped based on whether they had focal seizures that evolved into bilateral tonic-clonic seizures (17 with, 11 without). The trained neural network classified patients from controls with an accuracy of 72.92%, while the seizure subtype groups achieved a classification accuracy of 67.86%. In the patient subgroups, the nodes and edges deemed important for accurate classification were also clinically relevant, indicating the model’s interpretability. The current work expands the evidence for the potential of deep learning to extract relevant markers from clinical datasets. Our findings offer a rationale for further research interrogating structural connectomes to obtain features that can be biomarkers and aid the diagnosis of seizure subtypes. Oxford University Press 2023-10-31 /pmc/articles/PMC10644981/ /pubmed/38025275 http://dx.doi.org/10.1093/braincomms/fcad294 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Maher, Christina Tang, Zihao D’Souza, Arkiev Cabezas, Mariano Cai, Weidong Barnett, Michael Kavehei, Omid Wang, Chenyu Nikpour, Armin Deep learning distinguishes connectomes from focal epilepsy patients and controls: feasibility and clinical implications |
title | Deep learning distinguishes connectomes from focal epilepsy patients and controls: feasibility and clinical implications |
title_full | Deep learning distinguishes connectomes from focal epilepsy patients and controls: feasibility and clinical implications |
title_fullStr | Deep learning distinguishes connectomes from focal epilepsy patients and controls: feasibility and clinical implications |
title_full_unstemmed | Deep learning distinguishes connectomes from focal epilepsy patients and controls: feasibility and clinical implications |
title_short | Deep learning distinguishes connectomes from focal epilepsy patients and controls: feasibility and clinical implications |
title_sort | deep learning distinguishes connectomes from focal epilepsy patients and controls: feasibility and clinical implications |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644981/ https://www.ncbi.nlm.nih.gov/pubmed/38025275 http://dx.doi.org/10.1093/braincomms/fcad294 |
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