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Glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography

Changes in retinal vasculature and ocular circulation may play an important role in the glaucoma development and progression. We evaluated the vertical asymmetry across the temporal raphe of the deep retinal layer vessel density, using swept-source optical coherence tomography angiography (SS-OCTA),...

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Autores principales: Yoshikawa, Yuji, Shoji, Takuhei, Kanno, Junji, Ibuki, Hisashi, Weinreb, Robert N., Araie, Makoto, Shinoda, Kei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176726/
https://www.ncbi.nlm.nih.gov/pubmed/32322012
http://dx.doi.org/10.1038/s41598-020-63931-7
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author Yoshikawa, Yuji
Shoji, Takuhei
Kanno, Junji
Ibuki, Hisashi
Weinreb, Robert N.
Araie, Makoto
Shinoda, Kei
author_facet Yoshikawa, Yuji
Shoji, Takuhei
Kanno, Junji
Ibuki, Hisashi
Weinreb, Robert N.
Araie, Makoto
Shinoda, Kei
author_sort Yoshikawa, Yuji
collection PubMed
description Changes in retinal vasculature and ocular circulation may play an important role in the glaucoma development and progression. We evaluated the vertical asymmetry across the temporal raphe of the deep retinal layer vessel density, using swept-source optical coherence tomography angiography (SS-OCTA), and its relationship with the central visual field (VF) loss. Thirty-four eyes of 27 patients with open-angle glaucoma were included. SS-OCTA macular scanning was performed within a 3 × 3 mm (300 × 300 pixels) volume, centred on the fovea. The relationships between the vertical asymmetrical deep retinal vessel density reduction (ADRVD) across the temporal raphe and various ocular parameters were analysed. Twenty-two glaucomatous eyes with ADRVDs had central VF loss. Contrarily, ADRVDs were not found in any of the 12 eyes without central VF loss. Thirteen eyes (59.1%) with central VF loss had ADRVDs topographically corresponding to the central VF loss and macular ganglion cell complex thinning. The glaucomatous eyes with ADRVDs exhibited inferior rather than superior central VF loss (P = 0.032). Thus, ADRVD specifically indicates the glaucomatous central visual loss. Further analysis of ADRVD may improve our understanding on glaucoma pathogenesis, offering new treatment insights.
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spelling pubmed-71767262020-04-27 Glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography Yoshikawa, Yuji Shoji, Takuhei Kanno, Junji Ibuki, Hisashi Weinreb, Robert N. Araie, Makoto Shinoda, Kei Sci Rep Article Changes in retinal vasculature and ocular circulation may play an important role in the glaucoma development and progression. We evaluated the vertical asymmetry across the temporal raphe of the deep retinal layer vessel density, using swept-source optical coherence tomography angiography (SS-OCTA), and its relationship with the central visual field (VF) loss. Thirty-four eyes of 27 patients with open-angle glaucoma were included. SS-OCTA macular scanning was performed within a 3 × 3 mm (300 × 300 pixels) volume, centred on the fovea. The relationships between the vertical asymmetrical deep retinal vessel density reduction (ADRVD) across the temporal raphe and various ocular parameters were analysed. Twenty-two glaucomatous eyes with ADRVDs had central VF loss. Contrarily, ADRVDs were not found in any of the 12 eyes without central VF loss. Thirteen eyes (59.1%) with central VF loss had ADRVDs topographically corresponding to the central VF loss and macular ganglion cell complex thinning. The glaucomatous eyes with ADRVDs exhibited inferior rather than superior central VF loss (P = 0.032). Thus, ADRVD specifically indicates the glaucomatous central visual loss. Further analysis of ADRVD may improve our understanding on glaucoma pathogenesis, offering new treatment insights. Nature Publishing Group UK 2020-04-22 /pmc/articles/PMC7176726/ /pubmed/32322012 http://dx.doi.org/10.1038/s41598-020-63931-7 Text en © The Author(s) 2020 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
Yoshikawa, Yuji
Shoji, Takuhei
Kanno, Junji
Ibuki, Hisashi
Weinreb, Robert N.
Araie, Makoto
Shinoda, Kei
Glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography
title Glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography
title_full Glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography
title_fullStr Glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography
title_full_unstemmed Glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography
title_short Glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography
title_sort glaucomatous vertical vessel density asymmetry of the temporal raphe detected with optical coherence tomography angiography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176726/
https://www.ncbi.nlm.nih.gov/pubmed/32322012
http://dx.doi.org/10.1038/s41598-020-63931-7
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