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Evaluation of retinal pigment epithelium changes in serous pigment epithelial detachment in age-related macular degeneration

The purpose of this study was to quantitatively evaluate retinal pigment epithelium (RPE) changes in serous pigment epithelial detachment (PED) among patients with age-related macular degeneration by means of prototype multi-contrast optical coherence tomography (OCT), which is capable of simultaneo...

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Autores principales: Miura, Masahiro, Makita, Shuichi, Yasuno, Yoshiaki, Iwasaki, Takuya, Azuma, Shinnosuke, Mino, Toshihiro, Yamaguchi, Tatsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854605/
https://www.ncbi.nlm.nih.gov/pubmed/33531591
http://dx.doi.org/10.1038/s41598-021-82563-z
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author Miura, Masahiro
Makita, Shuichi
Yasuno, Yoshiaki
Iwasaki, Takuya
Azuma, Shinnosuke
Mino, Toshihiro
Yamaguchi, Tatsuo
author_facet Miura, Masahiro
Makita, Shuichi
Yasuno, Yoshiaki
Iwasaki, Takuya
Azuma, Shinnosuke
Mino, Toshihiro
Yamaguchi, Tatsuo
author_sort Miura, Masahiro
collection PubMed
description The purpose of this study was to quantitatively evaluate retinal pigment epithelium (RPE) changes in serous pigment epithelial detachment (PED) among patients with age-related macular degeneration by means of prototype multi-contrast optical coherence tomography (OCT), which is capable of simultaneous collection of OCT angiography, polarization-sensitive OCT, and standard OCT images. We evaluated 26 eyes of 21 patients with serous PED. RPE-melanin OCT images were calculated from the multi-contrast OCT dataset and compared with near-infrared autofluorescence images. An active RPE lesion was defined as an area of thickened RPE-melanin (≥ 70 μm; RPE(70)) on RPE-melanin OCT. Each PED area was divided into peak and slope regions. RPE(70) area ratios were compared with the maximum PED height, PED area, PED volume, and slope area ratio (area of slope region/area of whole PED). RPE-melanin OCT images were consistent with near-infrared autofluorescence images. The RPE(70) area ratio in the slope region was significantly negatively correlated with the slope area ratio. Development of active RPE lesions in the slope region was correlated with the PED configuration. Multi-contrast OCT is useful for objective evaluation of changes in the RPE in patients with age-related macular degeneration.
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spelling pubmed-78546052021-02-03 Evaluation of retinal pigment epithelium changes in serous pigment epithelial detachment in age-related macular degeneration Miura, Masahiro Makita, Shuichi Yasuno, Yoshiaki Iwasaki, Takuya Azuma, Shinnosuke Mino, Toshihiro Yamaguchi, Tatsuo Sci Rep Article The purpose of this study was to quantitatively evaluate retinal pigment epithelium (RPE) changes in serous pigment epithelial detachment (PED) among patients with age-related macular degeneration by means of prototype multi-contrast optical coherence tomography (OCT), which is capable of simultaneous collection of OCT angiography, polarization-sensitive OCT, and standard OCT images. We evaluated 26 eyes of 21 patients with serous PED. RPE-melanin OCT images were calculated from the multi-contrast OCT dataset and compared with near-infrared autofluorescence images. An active RPE lesion was defined as an area of thickened RPE-melanin (≥ 70 μm; RPE(70)) on RPE-melanin OCT. Each PED area was divided into peak and slope regions. RPE(70) area ratios were compared with the maximum PED height, PED area, PED volume, and slope area ratio (area of slope region/area of whole PED). RPE-melanin OCT images were consistent with near-infrared autofluorescence images. The RPE(70) area ratio in the slope region was significantly negatively correlated with the slope area ratio. Development of active RPE lesions in the slope region was correlated with the PED configuration. Multi-contrast OCT is useful for objective evaluation of changes in the RPE in patients with age-related macular degeneration. Nature Publishing Group UK 2021-02-02 /pmc/articles/PMC7854605/ /pubmed/33531591 http://dx.doi.org/10.1038/s41598-021-82563-z Text en © The Author(s) 2021 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/.
spellingShingle Article
Miura, Masahiro
Makita, Shuichi
Yasuno, Yoshiaki
Iwasaki, Takuya
Azuma, Shinnosuke
Mino, Toshihiro
Yamaguchi, Tatsuo
Evaluation of retinal pigment epithelium changes in serous pigment epithelial detachment in age-related macular degeneration
title Evaluation of retinal pigment epithelium changes in serous pigment epithelial detachment in age-related macular degeneration
title_full Evaluation of retinal pigment epithelium changes in serous pigment epithelial detachment in age-related macular degeneration
title_fullStr Evaluation of retinal pigment epithelium changes in serous pigment epithelial detachment in age-related macular degeneration
title_full_unstemmed Evaluation of retinal pigment epithelium changes in serous pigment epithelial detachment in age-related macular degeneration
title_short Evaluation of retinal pigment epithelium changes in serous pigment epithelial detachment in age-related macular degeneration
title_sort evaluation of retinal pigment epithelium changes in serous pigment epithelial detachment in age-related macular degeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854605/
https://www.ncbi.nlm.nih.gov/pubmed/33531591
http://dx.doi.org/10.1038/s41598-021-82563-z
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