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Fully-automated atrophy segmentation in dry age-related macular degeneration in optical coherence tomography

Age-related macular degeneration (AMD) is a progressive retinal disease, causing vision loss. A more detailed characterization of its atrophic form became possible thanks to the introduction of Optical Coherence Tomography (OCT). However, manual atrophy quantification in 3D retinal scans is a tediou...

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Autores principales: Derradji, Yasmine, Mosinska, Agata, Apostolopoulos, Stefanos, Ciller, Carlos, De Zanet, Sandro, Mantel, Irmela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8575929/
https://www.ncbi.nlm.nih.gov/pubmed/34751189
http://dx.doi.org/10.1038/s41598-021-01227-0
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author Derradji, Yasmine
Mosinska, Agata
Apostolopoulos, Stefanos
Ciller, Carlos
De Zanet, Sandro
Mantel, Irmela
author_facet Derradji, Yasmine
Mosinska, Agata
Apostolopoulos, Stefanos
Ciller, Carlos
De Zanet, Sandro
Mantel, Irmela
author_sort Derradji, Yasmine
collection PubMed
description Age-related macular degeneration (AMD) is a progressive retinal disease, causing vision loss. A more detailed characterization of its atrophic form became possible thanks to the introduction of Optical Coherence Tomography (OCT). However, manual atrophy quantification in 3D retinal scans is a tedious task and prevents taking full advantage of the accurate retina depiction. In this study we developed a fully automated algorithm segmenting Retinal Pigment Epithelial and Outer Retinal Atrophy (RORA) in dry AMD on macular OCT. 62 SD-OCT scans from eyes with atrophic AMD (57 patients) were collected and split into train and test sets. The training set was used to develop a Convolutional Neural Network (CNN). The performance of the algorithm was established by cross validation and comparison to the test set with ground-truth annotated by two graders. Additionally, the effect of using retinal layer segmentation during training was investigated. The algorithm achieved mean Dice scores of 0.881 and 0.844, sensitivity of 0.850 and 0.915 and precision of 0.928 and 0.799 in comparison with Expert 1 and Expert 2, respectively. Using retinal layer segmentation improved the model performance. The proposed model identified RORA with performance matching human experts. It has a potential to rapidly identify atrophy with high consistency.
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spelling pubmed-85759292021-11-09 Fully-automated atrophy segmentation in dry age-related macular degeneration in optical coherence tomography Derradji, Yasmine Mosinska, Agata Apostolopoulos, Stefanos Ciller, Carlos De Zanet, Sandro Mantel, Irmela Sci Rep Article Age-related macular degeneration (AMD) is a progressive retinal disease, causing vision loss. A more detailed characterization of its atrophic form became possible thanks to the introduction of Optical Coherence Tomography (OCT). However, manual atrophy quantification in 3D retinal scans is a tedious task and prevents taking full advantage of the accurate retina depiction. In this study we developed a fully automated algorithm segmenting Retinal Pigment Epithelial and Outer Retinal Atrophy (RORA) in dry AMD on macular OCT. 62 SD-OCT scans from eyes with atrophic AMD (57 patients) were collected and split into train and test sets. The training set was used to develop a Convolutional Neural Network (CNN). The performance of the algorithm was established by cross validation and comparison to the test set with ground-truth annotated by two graders. Additionally, the effect of using retinal layer segmentation during training was investigated. The algorithm achieved mean Dice scores of 0.881 and 0.844, sensitivity of 0.850 and 0.915 and precision of 0.928 and 0.799 in comparison with Expert 1 and Expert 2, respectively. Using retinal layer segmentation improved the model performance. The proposed model identified RORA with performance matching human experts. It has a potential to rapidly identify atrophy with high consistency. Nature Publishing Group UK 2021-11-08 /pmc/articles/PMC8575929/ /pubmed/34751189 http://dx.doi.org/10.1038/s41598-021-01227-0 Text en © The Author(s) 2021 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
Derradji, Yasmine
Mosinska, Agata
Apostolopoulos, Stefanos
Ciller, Carlos
De Zanet, Sandro
Mantel, Irmela
Fully-automated atrophy segmentation in dry age-related macular degeneration in optical coherence tomography
title Fully-automated atrophy segmentation in dry age-related macular degeneration in optical coherence tomography
title_full Fully-automated atrophy segmentation in dry age-related macular degeneration in optical coherence tomography
title_fullStr Fully-automated atrophy segmentation in dry age-related macular degeneration in optical coherence tomography
title_full_unstemmed Fully-automated atrophy segmentation in dry age-related macular degeneration in optical coherence tomography
title_short Fully-automated atrophy segmentation in dry age-related macular degeneration in optical coherence tomography
title_sort fully-automated atrophy segmentation in dry age-related macular degeneration in optical coherence tomography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8575929/
https://www.ncbi.nlm.nih.gov/pubmed/34751189
http://dx.doi.org/10.1038/s41598-021-01227-0
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