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Predicting OCT biological marker localization from weak annotations
Recent developments in deep learning have shown success in accurately predicting the location of biological markers in Optical Coherence Tomography (OCT) volumes of patients with Age-Related Macular Degeneration (AMD) and Diabetic Retinopathy (DR). We propose a method that automatically locates biol...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10640596/ https://www.ncbi.nlm.nih.gov/pubmed/37952011 http://dx.doi.org/10.1038/s41598-023-47019-6 |
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author | Tejero, Javier Gamazo Neila, Pablo Márquez Kurmann, Thomas Gallardo, Mathias Zinkernagel, Martin Wolf, Sebastian Sznitman, Raphael |
author_facet | Tejero, Javier Gamazo Neila, Pablo Márquez Kurmann, Thomas Gallardo, Mathias Zinkernagel, Martin Wolf, Sebastian Sznitman, Raphael |
author_sort | Tejero, Javier Gamazo |
collection | PubMed |
description | Recent developments in deep learning have shown success in accurately predicting the location of biological markers in Optical Coherence Tomography (OCT) volumes of patients with Age-Related Macular Degeneration (AMD) and Diabetic Retinopathy (DR). We propose a method that automatically locates biological markers to the Early Treatment Diabetic Retinopathy Study (ETDRS) rings, only requiring B-scan-level presence annotations. We trained a neural network using 22,723 OCT B-Scans of 460 eyes (433 patients) with AMD and DR, annotated with slice-level labels for Intraretinal Fluid (IRF) and Subretinal Fluid (SRF). The neural network outputs were mapped into the corresponding ETDRS rings. We incorporated the class annotations and domain knowledge into a loss function to constrain the output with biologically plausible solutions. The method was tested on a set of OCT volumes with 322 eyes (189 patients) with Diabetic Macular Edema, with slice-level SRF and IRF presence annotations for the ETDRS rings. Our method accurately predicted the presence of IRF and SRF in each ETDRS ring, outperforming previous baselines even in the most challenging scenarios. Our model was also successfully applied to en-face marker segmentation and showed consistency within C-scans, despite not incorporating volume information in the training process. We achieved a correlation coefficient of 0.946 for the prediction of the IRF area. |
format | Online Article Text |
id | pubmed-10640596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-106405962023-11-11 Predicting OCT biological marker localization from weak annotations Tejero, Javier Gamazo Neila, Pablo Márquez Kurmann, Thomas Gallardo, Mathias Zinkernagel, Martin Wolf, Sebastian Sznitman, Raphael Sci Rep Article Recent developments in deep learning have shown success in accurately predicting the location of biological markers in Optical Coherence Tomography (OCT) volumes of patients with Age-Related Macular Degeneration (AMD) and Diabetic Retinopathy (DR). We propose a method that automatically locates biological markers to the Early Treatment Diabetic Retinopathy Study (ETDRS) rings, only requiring B-scan-level presence annotations. We trained a neural network using 22,723 OCT B-Scans of 460 eyes (433 patients) with AMD and DR, annotated with slice-level labels for Intraretinal Fluid (IRF) and Subretinal Fluid (SRF). The neural network outputs were mapped into the corresponding ETDRS rings. We incorporated the class annotations and domain knowledge into a loss function to constrain the output with biologically plausible solutions. The method was tested on a set of OCT volumes with 322 eyes (189 patients) with Diabetic Macular Edema, with slice-level SRF and IRF presence annotations for the ETDRS rings. Our method accurately predicted the presence of IRF and SRF in each ETDRS ring, outperforming previous baselines even in the most challenging scenarios. Our model was also successfully applied to en-face marker segmentation and showed consistency within C-scans, despite not incorporating volume information in the training process. We achieved a correlation coefficient of 0.946 for the prediction of the IRF area. Nature Publishing Group UK 2023-11-11 /pmc/articles/PMC10640596/ /pubmed/37952011 http://dx.doi.org/10.1038/s41598-023-47019-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Tejero, Javier Gamazo Neila, Pablo Márquez Kurmann, Thomas Gallardo, Mathias Zinkernagel, Martin Wolf, Sebastian Sznitman, Raphael Predicting OCT biological marker localization from weak annotations |
title | Predicting OCT biological marker localization from weak annotations |
title_full | Predicting OCT biological marker localization from weak annotations |
title_fullStr | Predicting OCT biological marker localization from weak annotations |
title_full_unstemmed | Predicting OCT biological marker localization from weak annotations |
title_short | Predicting OCT biological marker localization from weak annotations |
title_sort | predicting oct biological marker localization from weak annotations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10640596/ https://www.ncbi.nlm.nih.gov/pubmed/37952011 http://dx.doi.org/10.1038/s41598-023-47019-6 |
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