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Retinal vessel architecture and geometry are not impaired in normal-tension glaucoma

To investigate the associations between retinal vessel parameters and normal-tension glaucoma (NTG). We conducted a case–control study with a prospective cohort, allowing to record 23 cases of NTG. We matched NTG patient with one primary open-angle glaucoma (POAG) and one control per case by age, sy...

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Autores principales: Leveque, Anne-Sophie, Bouisse, Magali, Labarere, José, Trucco, Emanuele, Hogg, Stephen, MacGillivray, Tom, Aptel, Florent, Chiquet, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130140/
https://www.ncbi.nlm.nih.gov/pubmed/37185916
http://dx.doi.org/10.1038/s41598-023-33361-2
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author Leveque, Anne-Sophie
Bouisse, Magali
Labarere, José
Trucco, Emanuele
Hogg, Stephen
MacGillivray, Tom
Aptel, Florent
Chiquet, Christophe
author_facet Leveque, Anne-Sophie
Bouisse, Magali
Labarere, José
Trucco, Emanuele
Hogg, Stephen
MacGillivray, Tom
Aptel, Florent
Chiquet, Christophe
author_sort Leveque, Anne-Sophie
collection PubMed
description To investigate the associations between retinal vessel parameters and normal-tension glaucoma (NTG). We conducted a case–control study with a prospective cohort, allowing to record 23 cases of NTG. We matched NTG patient with one primary open-angle glaucoma (POAG) and one control per case by age, systemic hypertension, diabetes, and refraction. Central retinal artery equivalent (CRAE), central retinal venule equivalent (CRVE), Arteriole-To-Venule ratio (AVR), Fractal Dimension and tortuosity of the vascular network were measured using VAMPIRE software. Our sample consisted of 23 NTG, 23 POAG, and 23 control individuals, with a median age of 65 years (25–75th percentile, 56–74). No significant differences were observed in median values for CRAE (130.6 µm (25–75th percentile, 122.8; 137.0) for NTG, 128.4 µm (124.0; 132.9) for POAG, and 135.3 µm (123.3; 144.8) for controls, P = .23), CRVE (172.1 µm (160.0; 188.3), 172.8 µm (163.3; 181.6), and 175.9 µm (167.6; 188.4), P = .43), AVR (0.76, 0.75, 0.74, P = .71), tortuosity and fractal parameters across study groups. Vascular morphological parameters were not significantly associated with retinal nerve fiber layer thickness or mean deviation for the NTG and POAG groups. Our results suggest that vascular dysregulation in NTG does not modify the architecture and geometry of the retinal vessel network.
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spelling pubmed-101301402023-04-27 Retinal vessel architecture and geometry are not impaired in normal-tension glaucoma Leveque, Anne-Sophie Bouisse, Magali Labarere, José Trucco, Emanuele Hogg, Stephen MacGillivray, Tom Aptel, Florent Chiquet, Christophe Sci Rep Article To investigate the associations between retinal vessel parameters and normal-tension glaucoma (NTG). We conducted a case–control study with a prospective cohort, allowing to record 23 cases of NTG. We matched NTG patient with one primary open-angle glaucoma (POAG) and one control per case by age, systemic hypertension, diabetes, and refraction. Central retinal artery equivalent (CRAE), central retinal venule equivalent (CRVE), Arteriole-To-Venule ratio (AVR), Fractal Dimension and tortuosity of the vascular network were measured using VAMPIRE software. Our sample consisted of 23 NTG, 23 POAG, and 23 control individuals, with a median age of 65 years (25–75th percentile, 56–74). No significant differences were observed in median values for CRAE (130.6 µm (25–75th percentile, 122.8; 137.0) for NTG, 128.4 µm (124.0; 132.9) for POAG, and 135.3 µm (123.3; 144.8) for controls, P = .23), CRVE (172.1 µm (160.0; 188.3), 172.8 µm (163.3; 181.6), and 175.9 µm (167.6; 188.4), P = .43), AVR (0.76, 0.75, 0.74, P = .71), tortuosity and fractal parameters across study groups. Vascular morphological parameters were not significantly associated with retinal nerve fiber layer thickness or mean deviation for the NTG and POAG groups. Our results suggest that vascular dysregulation in NTG does not modify the architecture and geometry of the retinal vessel network. Nature Publishing Group UK 2023-04-25 /pmc/articles/PMC10130140/ /pubmed/37185916 http://dx.doi.org/10.1038/s41598-023-33361-2 Text en © The Author(s) 2023 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
Leveque, Anne-Sophie
Bouisse, Magali
Labarere, José
Trucco, Emanuele
Hogg, Stephen
MacGillivray, Tom
Aptel, Florent
Chiquet, Christophe
Retinal vessel architecture and geometry are not impaired in normal-tension glaucoma
title Retinal vessel architecture and geometry are not impaired in normal-tension glaucoma
title_full Retinal vessel architecture and geometry are not impaired in normal-tension glaucoma
title_fullStr Retinal vessel architecture and geometry are not impaired in normal-tension glaucoma
title_full_unstemmed Retinal vessel architecture and geometry are not impaired in normal-tension glaucoma
title_short Retinal vessel architecture and geometry are not impaired in normal-tension glaucoma
title_sort retinal vessel architecture and geometry are not impaired in normal-tension glaucoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130140/
https://www.ncbi.nlm.nih.gov/pubmed/37185916
http://dx.doi.org/10.1038/s41598-023-33361-2
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