Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Tejero, Javier Gamazo, Neila, Pablo Márquez, Kurmann, Thomas, Gallardo, Mathias, Zinkernagel, Martin, Wolf, Sebastian, Sznitman, Raphael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
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
_version_ 1785133790608228352
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
work_keys_str_mv AT tejerojaviergamazo predictingoctbiologicalmarkerlocalizationfromweakannotations
AT neilapablomarquez predictingoctbiologicalmarkerlocalizationfromweakannotations
AT kurmannthomas predictingoctbiologicalmarkerlocalizationfromweakannotations
AT gallardomathias predictingoctbiologicalmarkerlocalizationfromweakannotations
AT zinkernagelmartin predictingoctbiologicalmarkerlocalizationfromweakannotations
AT wolfsebastian predictingoctbiologicalmarkerlocalizationfromweakannotations
AT sznitmanraphael predictingoctbiologicalmarkerlocalizationfromweakannotations