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Relationship between Retinal Inner Nuclear Layer Thickness and Severity of Visual Field Loss in Glaucoma
Glaucoma is a disease characterized by pathologic changes in inner retinal layers, which are comprised of retinal ganglion cells (RGCs). As retinal ganglion cells (RGCs) cross over other retinal neurons that are connected by synapses, it is meaningful to investigate the outer retinal changes in glau...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514146/ https://www.ncbi.nlm.nih.gov/pubmed/28717139 http://dx.doi.org/10.1038/s41598-017-05282-4 |
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author | Kim, Eun Kyoung Park, Hae-Young Lopilly Park, Chan Kee |
author_facet | Kim, Eun Kyoung Park, Hae-Young Lopilly Park, Chan Kee |
author_sort | Kim, Eun Kyoung |
collection | PubMed |
description | Glaucoma is a disease characterized by pathologic changes in inner retinal layers, which are comprised of retinal ganglion cells (RGCs). As retinal ganglion cells (RGCs) cross over other retinal neurons that are connected by synapses, it is meaningful to investigate the outer retinal changes in glaucoma. We evaluated the association between thicknesses of segmented retinal layers in macular region and severity of visual field loss in open-angle glaucoma (OAG). This study involved 103 glaucomatous eyes. Retinal nerve fiber layer (RNFL), ganglion cell layer (GCL), inner plexiform layer (IPL), inner nuclear layer (INL), outer plexiform layer (OPL), and outer nuclear layer (ONL) thicknesses were measured at the macular level using the Spectral-domain optical coherence tomography with segmentation software. The functional losses were measured using 24-2 standard automated perimetry. Macular structure losses were positively correlated with functional loss for RNFL, GCL, and IPL (R = 0.550, 0.637, and 0.649, respectively, P < 0.001) and negatively correlated with INL (R = −0.295, P = 0.041). By multivariate regression analysis, INL thickness was significantly associated with visual field mean deviation (dB) and optic disc hemorrhage. These finding carefully suggest reactive responses of neuronal or glial cells located in the INL occur during glaucoma progression. |
format | Online Article Text |
id | pubmed-5514146 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55141462017-07-19 Relationship between Retinal Inner Nuclear Layer Thickness and Severity of Visual Field Loss in Glaucoma Kim, Eun Kyoung Park, Hae-Young Lopilly Park, Chan Kee Sci Rep Article Glaucoma is a disease characterized by pathologic changes in inner retinal layers, which are comprised of retinal ganglion cells (RGCs). As retinal ganglion cells (RGCs) cross over other retinal neurons that are connected by synapses, it is meaningful to investigate the outer retinal changes in glaucoma. We evaluated the association between thicknesses of segmented retinal layers in macular region and severity of visual field loss in open-angle glaucoma (OAG). This study involved 103 glaucomatous eyes. Retinal nerve fiber layer (RNFL), ganglion cell layer (GCL), inner plexiform layer (IPL), inner nuclear layer (INL), outer plexiform layer (OPL), and outer nuclear layer (ONL) thicknesses were measured at the macular level using the Spectral-domain optical coherence tomography with segmentation software. The functional losses were measured using 24-2 standard automated perimetry. Macular structure losses were positively correlated with functional loss for RNFL, GCL, and IPL (R = 0.550, 0.637, and 0.649, respectively, P < 0.001) and negatively correlated with INL (R = −0.295, P = 0.041). By multivariate regression analysis, INL thickness was significantly associated with visual field mean deviation (dB) and optic disc hemorrhage. These finding carefully suggest reactive responses of neuronal or glial cells located in the INL occur during glaucoma progression. Nature Publishing Group UK 2017-07-17 /pmc/articles/PMC5514146/ /pubmed/28717139 http://dx.doi.org/10.1038/s41598-017-05282-4 Text en © The Author(s) 2017 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 Kim, Eun Kyoung Park, Hae-Young Lopilly Park, Chan Kee Relationship between Retinal Inner Nuclear Layer Thickness and Severity of Visual Field Loss in Glaucoma |
title | Relationship between Retinal Inner Nuclear Layer Thickness and Severity of Visual Field Loss in Glaucoma |
title_full | Relationship between Retinal Inner Nuclear Layer Thickness and Severity of Visual Field Loss in Glaucoma |
title_fullStr | Relationship between Retinal Inner Nuclear Layer Thickness and Severity of Visual Field Loss in Glaucoma |
title_full_unstemmed | Relationship between Retinal Inner Nuclear Layer Thickness and Severity of Visual Field Loss in Glaucoma |
title_short | Relationship between Retinal Inner Nuclear Layer Thickness and Severity of Visual Field Loss in Glaucoma |
title_sort | relationship between retinal inner nuclear layer thickness and severity of visual field loss in glaucoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514146/ https://www.ncbi.nlm.nih.gov/pubmed/28717139 http://dx.doi.org/10.1038/s41598-017-05282-4 |
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