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Automatic Deep-Learning Segmentation of Epicardial Adipose Tissue from Low-Dose Chest CT and Prognosis Impact on COVID-19

Background: To develop a deep-learning (DL) pipeline that allowed an automated segmentation of epicardial adipose tissue (EAT) from low-dose computed tomography (LDCT) and investigate the link between EAT and COVID-19 clinical outcomes. Methods: This monocentric retrospective study included 353 pati...

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Autores principales: Bartoli, Axel, Fournel, Joris, Ait-Yahia, Léa, Cadour, Farah, Tradi, Farouk, Ghattas, Badih, Cortaredona, Sébastien, Million, Matthieu, Lasbleiz, Adèle, Dutour, Anne, Gaborit, Bénédicte, Jacquier, Alexis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947414/
https://www.ncbi.nlm.nih.gov/pubmed/35326485
http://dx.doi.org/10.3390/cells11061034
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author Bartoli, Axel
Fournel, Joris
Ait-Yahia, Léa
Cadour, Farah
Tradi, Farouk
Ghattas, Badih
Cortaredona, Sébastien
Million, Matthieu
Lasbleiz, Adèle
Dutour, Anne
Gaborit, Bénédicte
Jacquier, Alexis
author_facet Bartoli, Axel
Fournel, Joris
Ait-Yahia, Léa
Cadour, Farah
Tradi, Farouk
Ghattas, Badih
Cortaredona, Sébastien
Million, Matthieu
Lasbleiz, Adèle
Dutour, Anne
Gaborit, Bénédicte
Jacquier, Alexis
author_sort Bartoli, Axel
collection PubMed
description Background: To develop a deep-learning (DL) pipeline that allowed an automated segmentation of epicardial adipose tissue (EAT) from low-dose computed tomography (LDCT) and investigate the link between EAT and COVID-19 clinical outcomes. Methods: This monocentric retrospective study included 353 patients: 95 for training, 20 for testing, and 238 for prognosis evaluation. EAT segmentation was obtained after thresholding on a manually segmented pericardial volume. The model was evaluated with Dice coefficient (DSC), inter-and intraobserver reproducibility, and clinical measures. Uni-and multi-variate analyzes were conducted to assess the prognosis value of the EAT volume, EAT extent, and lung lesion extent on clinical outcomes, including hospitalization, oxygen therapy, intensive care unit admission and death. Results: The mean DSC for EAT volumes was 0.85 ± 0.05. For EAT volume, the mean absolute error was 11.7 ± 8.1 cm(3) with a non-significant bias of −4.0 ± 13.9 cm(3) and a correlation of 0.963 with the manual measures (p < 0.01). The multivariate model providing the higher AUC to predict adverse outcome include both EAT extent and lung lesion extent (AUC = 0.805). Conclusions: A DL algorithm was developed and evaluated to obtain reproducible and precise EAT segmentation on LDCT. EAT extent in association with lung lesion extent was associated with adverse clinical outcomes with an AUC = 0.805.
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spelling pubmed-89474142022-03-25 Automatic Deep-Learning Segmentation of Epicardial Adipose Tissue from Low-Dose Chest CT and Prognosis Impact on COVID-19 Bartoli, Axel Fournel, Joris Ait-Yahia, Léa Cadour, Farah Tradi, Farouk Ghattas, Badih Cortaredona, Sébastien Million, Matthieu Lasbleiz, Adèle Dutour, Anne Gaborit, Bénédicte Jacquier, Alexis Cells Article Background: To develop a deep-learning (DL) pipeline that allowed an automated segmentation of epicardial adipose tissue (EAT) from low-dose computed tomography (LDCT) and investigate the link between EAT and COVID-19 clinical outcomes. Methods: This monocentric retrospective study included 353 patients: 95 for training, 20 for testing, and 238 for prognosis evaluation. EAT segmentation was obtained after thresholding on a manually segmented pericardial volume. The model was evaluated with Dice coefficient (DSC), inter-and intraobserver reproducibility, and clinical measures. Uni-and multi-variate analyzes were conducted to assess the prognosis value of the EAT volume, EAT extent, and lung lesion extent on clinical outcomes, including hospitalization, oxygen therapy, intensive care unit admission and death. Results: The mean DSC for EAT volumes was 0.85 ± 0.05. For EAT volume, the mean absolute error was 11.7 ± 8.1 cm(3) with a non-significant bias of −4.0 ± 13.9 cm(3) and a correlation of 0.963 with the manual measures (p < 0.01). The multivariate model providing the higher AUC to predict adverse outcome include both EAT extent and lung lesion extent (AUC = 0.805). Conclusions: A DL algorithm was developed and evaluated to obtain reproducible and precise EAT segmentation on LDCT. EAT extent in association with lung lesion extent was associated with adverse clinical outcomes with an AUC = 0.805. MDPI 2022-03-18 /pmc/articles/PMC8947414/ /pubmed/35326485 http://dx.doi.org/10.3390/cells11061034 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bartoli, Axel
Fournel, Joris
Ait-Yahia, Léa
Cadour, Farah
Tradi, Farouk
Ghattas, Badih
Cortaredona, Sébastien
Million, Matthieu
Lasbleiz, Adèle
Dutour, Anne
Gaborit, Bénédicte
Jacquier, Alexis
Automatic Deep-Learning Segmentation of Epicardial Adipose Tissue from Low-Dose Chest CT and Prognosis Impact on COVID-19
title Automatic Deep-Learning Segmentation of Epicardial Adipose Tissue from Low-Dose Chest CT and Prognosis Impact on COVID-19
title_full Automatic Deep-Learning Segmentation of Epicardial Adipose Tissue from Low-Dose Chest CT and Prognosis Impact on COVID-19
title_fullStr Automatic Deep-Learning Segmentation of Epicardial Adipose Tissue from Low-Dose Chest CT and Prognosis Impact on COVID-19
title_full_unstemmed Automatic Deep-Learning Segmentation of Epicardial Adipose Tissue from Low-Dose Chest CT and Prognosis Impact on COVID-19
title_short Automatic Deep-Learning Segmentation of Epicardial Adipose Tissue from Low-Dose Chest CT and Prognosis Impact on COVID-19
title_sort automatic deep-learning segmentation of epicardial adipose tissue from low-dose chest ct and prognosis impact on covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947414/
https://www.ncbi.nlm.nih.gov/pubmed/35326485
http://dx.doi.org/10.3390/cells11061034
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