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Automated evaluation of retinal pigment epithelium disease area in eyes with age-related macular degeneration

The retinal pigment epithelium (RPE) is essential for the survival and function of retinal photoreceptor cells. RPE dysfunction causes various retinal diseases including age-related macular degeneration (AMD). Clinical studies on ES/iPS cell-derived RPE transplantation for RPE dysfunction-triggered...

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Autores principales: Motozawa, Naohiro, Miura, Takuya, Ochiai, Koji, Yamamoto, Midori, Horinouchi, Takaaki, Tsuzuki, Taku, Kanda, Genki N., Ozawa, Yosuke, Tsujikawa, Akitaka, Takahashi, Koichi, Takahashi, Masayo, Kurimoto, Yasuo, Maeda, Tadao, Mandai, Michiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766591/
https://www.ncbi.nlm.nih.gov/pubmed/35042966
http://dx.doi.org/10.1038/s41598-022-05006-3
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author Motozawa, Naohiro
Miura, Takuya
Ochiai, Koji
Yamamoto, Midori
Horinouchi, Takaaki
Tsuzuki, Taku
Kanda, Genki N.
Ozawa, Yosuke
Tsujikawa, Akitaka
Takahashi, Koichi
Takahashi, Masayo
Kurimoto, Yasuo
Maeda, Tadao
Mandai, Michiko
author_facet Motozawa, Naohiro
Miura, Takuya
Ochiai, Koji
Yamamoto, Midori
Horinouchi, Takaaki
Tsuzuki, Taku
Kanda, Genki N.
Ozawa, Yosuke
Tsujikawa, Akitaka
Takahashi, Koichi
Takahashi, Masayo
Kurimoto, Yasuo
Maeda, Tadao
Mandai, Michiko
author_sort Motozawa, Naohiro
collection PubMed
description The retinal pigment epithelium (RPE) is essential for the survival and function of retinal photoreceptor cells. RPE dysfunction causes various retinal diseases including age-related macular degeneration (AMD). Clinical studies on ES/iPS cell-derived RPE transplantation for RPE dysfunction-triggered diseases are currently underway. Quantification of the diseased RPE area is important to evaluate disease progression or the therapeutic effect of RPE transplantation. However, there are no standard protocols. To address this issue, we developed a 2-step software that enables objective and efficient quantification of RPE-disease area changes by analyzing the early-phase hyperfluorescent area in fluorescein angiography (FA) images. We extracted the Abnormal region. This extraction was based on deep learning-based discrimination. We scored the binarized extracted area using an automated program. Our program’s performance for the same eye from the serial image captures was within 3.1 ± 7.8% error. In progressive AMD, the trend was consistent with human assessment, even when FA images from two different visits were compared. This method was applicable to quantifying RPE-disease area changes over time, evaluating iPSC-RPE transplantation images, and a disease other than AMD. Our program may contribute to the assessment of the clinical course of RPE-disease areas in routine clinics and reduce the workload of researchers.
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spelling pubmed-87665912022-01-20 Automated evaluation of retinal pigment epithelium disease area in eyes with age-related macular degeneration Motozawa, Naohiro Miura, Takuya Ochiai, Koji Yamamoto, Midori Horinouchi, Takaaki Tsuzuki, Taku Kanda, Genki N. Ozawa, Yosuke Tsujikawa, Akitaka Takahashi, Koichi Takahashi, Masayo Kurimoto, Yasuo Maeda, Tadao Mandai, Michiko Sci Rep Article The retinal pigment epithelium (RPE) is essential for the survival and function of retinal photoreceptor cells. RPE dysfunction causes various retinal diseases including age-related macular degeneration (AMD). Clinical studies on ES/iPS cell-derived RPE transplantation for RPE dysfunction-triggered diseases are currently underway. Quantification of the diseased RPE area is important to evaluate disease progression or the therapeutic effect of RPE transplantation. However, there are no standard protocols. To address this issue, we developed a 2-step software that enables objective and efficient quantification of RPE-disease area changes by analyzing the early-phase hyperfluorescent area in fluorescein angiography (FA) images. We extracted the Abnormal region. This extraction was based on deep learning-based discrimination. We scored the binarized extracted area using an automated program. Our program’s performance for the same eye from the serial image captures was within 3.1 ± 7.8% error. In progressive AMD, the trend was consistent with human assessment, even when FA images from two different visits were compared. This method was applicable to quantifying RPE-disease area changes over time, evaluating iPSC-RPE transplantation images, and a disease other than AMD. Our program may contribute to the assessment of the clinical course of RPE-disease areas in routine clinics and reduce the workload of researchers. Nature Publishing Group UK 2022-01-18 /pmc/articles/PMC8766591/ /pubmed/35042966 http://dx.doi.org/10.1038/s41598-022-05006-3 Text en © The Author(s) 2022 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
Motozawa, Naohiro
Miura, Takuya
Ochiai, Koji
Yamamoto, Midori
Horinouchi, Takaaki
Tsuzuki, Taku
Kanda, Genki N.
Ozawa, Yosuke
Tsujikawa, Akitaka
Takahashi, Koichi
Takahashi, Masayo
Kurimoto, Yasuo
Maeda, Tadao
Mandai, Michiko
Automated evaluation of retinal pigment epithelium disease area in eyes with age-related macular degeneration
title Automated evaluation of retinal pigment epithelium disease area in eyes with age-related macular degeneration
title_full Automated evaluation of retinal pigment epithelium disease area in eyes with age-related macular degeneration
title_fullStr Automated evaluation of retinal pigment epithelium disease area in eyes with age-related macular degeneration
title_full_unstemmed Automated evaluation of retinal pigment epithelium disease area in eyes with age-related macular degeneration
title_short Automated evaluation of retinal pigment epithelium disease area in eyes with age-related macular degeneration
title_sort automated evaluation of retinal pigment epithelium disease area in eyes with age-related macular degeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766591/
https://www.ncbi.nlm.nih.gov/pubmed/35042966
http://dx.doi.org/10.1038/s41598-022-05006-3
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