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Association between peripapillary scleral deformation and choroidal microvascular circulation in glaucoma
Peripapillary vessel density, which is reduced in eyes with glaucoma, has been proposed as a diagnostic tool for the desease and peripapillary choroidal microvasculature dropout(MvD) is considered one of pathophysiological manifestation of glaucomatous damage. However, little is known about the unde...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6898378/ https://www.ncbi.nlm.nih.gov/pubmed/31811238 http://dx.doi.org/10.1038/s41598-019-54882-9 |
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author | Shin, Da Young Jeon, Soo Ji Kim, Eun Kyoung Jung, Kyoung In Park, Hae Young Lopilly Park, Chan Kee |
author_facet | Shin, Da Young Jeon, Soo Ji Kim, Eun Kyoung Jung, Kyoung In Park, Hae Young Lopilly Park, Chan Kee |
author_sort | Shin, Da Young |
collection | PubMed |
description | Peripapillary vessel density, which is reduced in eyes with glaucoma, has been proposed as a diagnostic tool for the desease and peripapillary choroidal microvasculature dropout(MvD) is considered one of pathophysiological manifestation of glaucomatous damage. However, little is known about the underlying pathogenic mechanism of dropout. According to recent studies, MvD is associated with structural changes in ONH structures. Therefore, we investigated the association between peripapillary scleral deformation and MvD. Data from 62 open-angle glaucoma (OAG) eyes with MvD and 36 eyes without MvD were analyzed in this study. And eyes with MvD were classified into two groups based on location: a juxtapapillary group and a non-juxtapapillary group for further analysis. More eyes with MvD had focal scleral deformation than did those without MvD (64.5% versus 2.8%; P < 0.001). Peripapillary choroidal thickness and focal scleral deformation were significantly associated with MvD. And juxtapapillary group was more associated with focal scleral deformation and coincidental RNFL defects than non-juxtapapillary groups. Peripapillary choroidal MvD was associated with the presence of scleral deformation, especially with juxtapapillary MvD, which was related to corresponding RNFL defects. |
format | Online Article Text |
id | pubmed-6898378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68983782019-12-12 Association between peripapillary scleral deformation and choroidal microvascular circulation in glaucoma Shin, Da Young Jeon, Soo Ji Kim, Eun Kyoung Jung, Kyoung In Park, Hae Young Lopilly Park, Chan Kee Sci Rep Article Peripapillary vessel density, which is reduced in eyes with glaucoma, has been proposed as a diagnostic tool for the desease and peripapillary choroidal microvasculature dropout(MvD) is considered one of pathophysiological manifestation of glaucomatous damage. However, little is known about the underlying pathogenic mechanism of dropout. According to recent studies, MvD is associated with structural changes in ONH structures. Therefore, we investigated the association between peripapillary scleral deformation and MvD. Data from 62 open-angle glaucoma (OAG) eyes with MvD and 36 eyes without MvD were analyzed in this study. And eyes with MvD were classified into two groups based on location: a juxtapapillary group and a non-juxtapapillary group for further analysis. More eyes with MvD had focal scleral deformation than did those without MvD (64.5% versus 2.8%; P < 0.001). Peripapillary choroidal thickness and focal scleral deformation were significantly associated with MvD. And juxtapapillary group was more associated with focal scleral deformation and coincidental RNFL defects than non-juxtapapillary groups. Peripapillary choroidal MvD was associated with the presence of scleral deformation, especially with juxtapapillary MvD, which was related to corresponding RNFL defects. Nature Publishing Group UK 2019-12-06 /pmc/articles/PMC6898378/ /pubmed/31811238 http://dx.doi.org/10.1038/s41598-019-54882-9 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 Shin, Da Young Jeon, Soo Ji Kim, Eun Kyoung Jung, Kyoung In Park, Hae Young Lopilly Park, Chan Kee Association between peripapillary scleral deformation and choroidal microvascular circulation in glaucoma |
title | Association between peripapillary scleral deformation and choroidal microvascular circulation in glaucoma |
title_full | Association between peripapillary scleral deformation and choroidal microvascular circulation in glaucoma |
title_fullStr | Association between peripapillary scleral deformation and choroidal microvascular circulation in glaucoma |
title_full_unstemmed | Association between peripapillary scleral deformation and choroidal microvascular circulation in glaucoma |
title_short | Association between peripapillary scleral deformation and choroidal microvascular circulation in glaucoma |
title_sort | association between peripapillary scleral deformation and choroidal microvascular circulation in glaucoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6898378/ https://www.ncbi.nlm.nih.gov/pubmed/31811238 http://dx.doi.org/10.1038/s41598-019-54882-9 |
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