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Predicting risk of late age-related macular degeneration using deep learning
By 2040, age-related macular degeneration (AMD) will affect ~288 million people worldwide. Identifying individuals at high risk of progression to late AMD, the sight-threatening stage, is critical for clinical actions, including medical interventions and timely monitoring. Although deep learning has...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453007/ https://www.ncbi.nlm.nih.gov/pubmed/32904246 http://dx.doi.org/10.1038/s41746-020-00317-z |
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author | Peng, Yifan Keenan, Tiarnan D. Chen, Qingyu Agrón, Elvira Allot, Alexis Wong, Wai T. Chew, Emily Y. Lu, Zhiyong |
author_facet | Peng, Yifan Keenan, Tiarnan D. Chen, Qingyu Agrón, Elvira Allot, Alexis Wong, Wai T. Chew, Emily Y. Lu, Zhiyong |
author_sort | Peng, Yifan |
collection | PubMed |
description | By 2040, age-related macular degeneration (AMD) will affect ~288 million people worldwide. Identifying individuals at high risk of progression to late AMD, the sight-threatening stage, is critical for clinical actions, including medical interventions and timely monitoring. Although deep learning has shown promise in diagnosing/screening AMD using color fundus photographs, it remains difficult to predict individuals’ risks of late AMD accurately. For both tasks, these initial deep learning attempts have remained largely unvalidated in independent cohorts. Here, we demonstrate how deep learning and survival analysis can predict the probability of progression to late AMD using 3298 participants (over 80,000 images) from the Age-Related Eye Disease Studies AREDS and AREDS2, the largest longitudinal clinical trials in AMD. When validated against an independent test data set of 601 participants, our model achieved high prognostic accuracy (5-year C-statistic 86.4 (95% confidence interval 86.2–86.6)) that substantially exceeded that of retinal specialists using two existing clinical standards (81.3 (81.1–81.5) and 82.0 (81.8–82.3), respectively). Interestingly, our approach offers additional strengths over the existing clinical standards in AMD prognosis (e.g., risk ascertainment above 50%) and is likely to be highly generalizable, given the breadth of training data from 82 US retinal specialty clinics. Indeed, during external validation through training on AREDS and testing on AREDS2 as an independent cohort, our model retained substantially higher prognostic accuracy than existing clinical standards. These results highlight the potential of deep learning systems to enhance clinical decision-making in AMD patients. |
format | Online Article Text |
id | pubmed-7453007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74530072020-09-03 Predicting risk of late age-related macular degeneration using deep learning Peng, Yifan Keenan, Tiarnan D. Chen, Qingyu Agrón, Elvira Allot, Alexis Wong, Wai T. Chew, Emily Y. Lu, Zhiyong NPJ Digit Med Article By 2040, age-related macular degeneration (AMD) will affect ~288 million people worldwide. Identifying individuals at high risk of progression to late AMD, the sight-threatening stage, is critical for clinical actions, including medical interventions and timely monitoring. Although deep learning has shown promise in diagnosing/screening AMD using color fundus photographs, it remains difficult to predict individuals’ risks of late AMD accurately. For both tasks, these initial deep learning attempts have remained largely unvalidated in independent cohorts. Here, we demonstrate how deep learning and survival analysis can predict the probability of progression to late AMD using 3298 participants (over 80,000 images) from the Age-Related Eye Disease Studies AREDS and AREDS2, the largest longitudinal clinical trials in AMD. When validated against an independent test data set of 601 participants, our model achieved high prognostic accuracy (5-year C-statistic 86.4 (95% confidence interval 86.2–86.6)) that substantially exceeded that of retinal specialists using two existing clinical standards (81.3 (81.1–81.5) and 82.0 (81.8–82.3), respectively). Interestingly, our approach offers additional strengths over the existing clinical standards in AMD prognosis (e.g., risk ascertainment above 50%) and is likely to be highly generalizable, given the breadth of training data from 82 US retinal specialty clinics. Indeed, during external validation through training on AREDS and testing on AREDS2 as an independent cohort, our model retained substantially higher prognostic accuracy than existing clinical standards. These results highlight the potential of deep learning systems to enhance clinical decision-making in AMD patients. Nature Publishing Group UK 2020-08-27 /pmc/articles/PMC7453007/ /pubmed/32904246 http://dx.doi.org/10.1038/s41746-020-00317-z Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2020 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 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Peng, Yifan Keenan, Tiarnan D. Chen, Qingyu Agrón, Elvira Allot, Alexis Wong, Wai T. Chew, Emily Y. Lu, Zhiyong Predicting risk of late age-related macular degeneration using deep learning |
title | Predicting risk of late age-related macular degeneration using deep learning |
title_full | Predicting risk of late age-related macular degeneration using deep learning |
title_fullStr | Predicting risk of late age-related macular degeneration using deep learning |
title_full_unstemmed | Predicting risk of late age-related macular degeneration using deep learning |
title_short | Predicting risk of late age-related macular degeneration using deep learning |
title_sort | predicting risk of late age-related macular degeneration using deep learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7453007/ https://www.ncbi.nlm.nih.gov/pubmed/32904246 http://dx.doi.org/10.1038/s41746-020-00317-z |
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