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Automated detection and classification of early AMD biomarkers using deep learning

Age-related macular degeneration (AMD) affects millions of people and is a leading cause of blindness throughout the world. Ideally, affected individuals would be identified at an early stage before late sequelae such as outer retinal atrophy or exudative neovascular membranes develop, which could p...

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Autores principales: Saha, Sajib, Nassisi, Marco, Wang, Mo, Lindenberg, Sophiana, kanagasingam, Yogi, Sadda, Srinivas, Hu, Zhihong Jewel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662691/
https://www.ncbi.nlm.nih.gov/pubmed/31358808
http://dx.doi.org/10.1038/s41598-019-47390-3
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author Saha, Sajib
Nassisi, Marco
Wang, Mo
Lindenberg, Sophiana
kanagasingam, Yogi
Sadda, Srinivas
Hu, Zhihong Jewel
author_facet Saha, Sajib
Nassisi, Marco
Wang, Mo
Lindenberg, Sophiana
kanagasingam, Yogi
Sadda, Srinivas
Hu, Zhihong Jewel
author_sort Saha, Sajib
collection PubMed
description Age-related macular degeneration (AMD) affects millions of people and is a leading cause of blindness throughout the world. Ideally, affected individuals would be identified at an early stage before late sequelae such as outer retinal atrophy or exudative neovascular membranes develop, which could produce irreversible visual loss. Early identification could allow patients to be staged and appropriate monitoring intervals to be established. Accurate staging of earlier AMD stages could also facilitate the development of new preventative therapeutics. However, accurate and precise staging of AMD, particularly using newer optical coherence tomography (OCT)-based biomarkers may be time-intensive and requires expert training which may not feasible in many circumstances, particularly in screening settings. In this work we develop deep learning method for automated detection and classification of early AMD OCT biomarker. Deep convolution neural networks (CNN) were explicitly trained for performing automated detection and classification of hyperreflective foci, hyporeflective foci within the drusen, and subretinal drusenoid deposits from OCT B-scans. Numerous experiments were conducted to evaluate the performance of several state-of-the-art CNNs and different transfer learning protocols on an image dataset containing approximately 20000 OCT B-scans from 153 patients. An overall accuracy of 87% for identifying the presence of early AMD biomarkers was achieved.
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spelling pubmed-66626912019-08-02 Automated detection and classification of early AMD biomarkers using deep learning Saha, Sajib Nassisi, Marco Wang, Mo Lindenberg, Sophiana kanagasingam, Yogi Sadda, Srinivas Hu, Zhihong Jewel Sci Rep Article Age-related macular degeneration (AMD) affects millions of people and is a leading cause of blindness throughout the world. Ideally, affected individuals would be identified at an early stage before late sequelae such as outer retinal atrophy or exudative neovascular membranes develop, which could produce irreversible visual loss. Early identification could allow patients to be staged and appropriate monitoring intervals to be established. Accurate staging of earlier AMD stages could also facilitate the development of new preventative therapeutics. However, accurate and precise staging of AMD, particularly using newer optical coherence tomography (OCT)-based biomarkers may be time-intensive and requires expert training which may not feasible in many circumstances, particularly in screening settings. In this work we develop deep learning method for automated detection and classification of early AMD OCT biomarker. Deep convolution neural networks (CNN) were explicitly trained for performing automated detection and classification of hyperreflective foci, hyporeflective foci within the drusen, and subretinal drusenoid deposits from OCT B-scans. Numerous experiments were conducted to evaluate the performance of several state-of-the-art CNNs and different transfer learning protocols on an image dataset containing approximately 20000 OCT B-scans from 153 patients. An overall accuracy of 87% for identifying the presence of early AMD biomarkers was achieved. Nature Publishing Group UK 2019-07-29 /pmc/articles/PMC6662691/ /pubmed/31358808 http://dx.doi.org/10.1038/s41598-019-47390-3 Text en © The Author(s) 2019 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Saha, Sajib
Nassisi, Marco
Wang, Mo
Lindenberg, Sophiana
kanagasingam, Yogi
Sadda, Srinivas
Hu, Zhihong Jewel
Automated detection and classification of early AMD biomarkers using deep learning
title Automated detection and classification of early AMD biomarkers using deep learning
title_full Automated detection and classification of early AMD biomarkers using deep learning
title_fullStr Automated detection and classification of early AMD biomarkers using deep learning
title_full_unstemmed Automated detection and classification of early AMD biomarkers using deep learning
title_short Automated detection and classification of early AMD biomarkers using deep learning
title_sort automated detection and classification of early amd biomarkers using deep learning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662691/
https://www.ncbi.nlm.nih.gov/pubmed/31358808
http://dx.doi.org/10.1038/s41598-019-47390-3
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