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Comparison of glaucoma diagnostic ability of ganglion cell-inner plexiform layer according to the range around the fovea

BACKGROUND: To compare the glaucoma diagnostic ability of the ganglion cell-inner plexiform layer (GCIPL) thickness depending on the range around the fovea using wide-angle, swept-source optical coherence tomography (SS-OCT). METHODS: We compared the glaucoma diagnostic utility of GCIPL parameters a...

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Autores principales: Jung, Jae Ho, Seo, Je Hyun, Kang, Min Seung, Shin, Jonghoon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937720/
https://www.ncbi.nlm.nih.gov/pubmed/31888556
http://dx.doi.org/10.1186/s12886-019-1283-y
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author Jung, Jae Ho
Seo, Je Hyun
Kang, Min Seung
Shin, Jonghoon
author_facet Jung, Jae Ho
Seo, Je Hyun
Kang, Min Seung
Shin, Jonghoon
author_sort Jung, Jae Ho
collection PubMed
description BACKGROUND: To compare the glaucoma diagnostic ability of the ganglion cell-inner plexiform layer (GCIPL) thickness depending on the range around the fovea using wide-angle, swept-source optical coherence tomography (SS-OCT). METHODS: We compared the glaucoma diagnostic utility of GCIPL parameters across multiple regions while centered on the fovea. In a wide-angle scan, the GCIPL for each 1-mm(2) grid square of a 12 × 9 mm(2) scan resulted in 108 data points. With respect to the range of the GCIPL measurements around the macula, the wide-angle scan images were classified into three zones. Zone 1 was defined as a narrow area; zone 2 was defined as a mid-sized area; and zone 3 was defined as a wide area. We recorded the quadrant GCIPL thickness, average, and minimum quadrant GCIPL within each zone. The areas under the receiver operating characteristic (AUROCs) curves were calculated to evaluate the glaucoma diagnostic utility. RESULTS: Sixty-one eyes with glaucoma and 59 normal eyes were assessed. The minimum and average GCIPL measurements in zones 1–3 in eyes with glaucoma were significantly lower than those in normal eyes (P <  0.001). The AUROCs for the minimum and inferotemporal GCIPL in zone 1 and the inferotemporal GCIPL thickness in zone 2 were greater than 0.9 (0.945, 0.931, and 0.918, respectively). CONCLUSIONS: Wide-angle scanning using SS-OCT will contribute to improvements in the detection of glaucomatous damage. The minimum and inferotemporal GCIPL in zone 1 may be more useful for detecting glaucoma than those in the conventional area.
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spelling pubmed-69377202019-12-31 Comparison of glaucoma diagnostic ability of ganglion cell-inner plexiform layer according to the range around the fovea Jung, Jae Ho Seo, Je Hyun Kang, Min Seung Shin, Jonghoon BMC Ophthalmol Research Article BACKGROUND: To compare the glaucoma diagnostic ability of the ganglion cell-inner plexiform layer (GCIPL) thickness depending on the range around the fovea using wide-angle, swept-source optical coherence tomography (SS-OCT). METHODS: We compared the glaucoma diagnostic utility of GCIPL parameters across multiple regions while centered on the fovea. In a wide-angle scan, the GCIPL for each 1-mm(2) grid square of a 12 × 9 mm(2) scan resulted in 108 data points. With respect to the range of the GCIPL measurements around the macula, the wide-angle scan images were classified into three zones. Zone 1 was defined as a narrow area; zone 2 was defined as a mid-sized area; and zone 3 was defined as a wide area. We recorded the quadrant GCIPL thickness, average, and minimum quadrant GCIPL within each zone. The areas under the receiver operating characteristic (AUROCs) curves were calculated to evaluate the glaucoma diagnostic utility. RESULTS: Sixty-one eyes with glaucoma and 59 normal eyes were assessed. The minimum and average GCIPL measurements in zones 1–3 in eyes with glaucoma were significantly lower than those in normal eyes (P <  0.001). The AUROCs for the minimum and inferotemporal GCIPL in zone 1 and the inferotemporal GCIPL thickness in zone 2 were greater than 0.9 (0.945, 0.931, and 0.918, respectively). CONCLUSIONS: Wide-angle scanning using SS-OCT will contribute to improvements in the detection of glaucomatous damage. The minimum and inferotemporal GCIPL in zone 1 may be more useful for detecting glaucoma than those in the conventional area. BioMed Central 2019-12-30 /pmc/articles/PMC6937720/ /pubmed/31888556 http://dx.doi.org/10.1186/s12886-019-1283-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Jung, Jae Ho
Seo, Je Hyun
Kang, Min Seung
Shin, Jonghoon
Comparison of glaucoma diagnostic ability of ganglion cell-inner plexiform layer according to the range around the fovea
title Comparison of glaucoma diagnostic ability of ganglion cell-inner plexiform layer according to the range around the fovea
title_full Comparison of glaucoma diagnostic ability of ganglion cell-inner plexiform layer according to the range around the fovea
title_fullStr Comparison of glaucoma diagnostic ability of ganglion cell-inner plexiform layer according to the range around the fovea
title_full_unstemmed Comparison of glaucoma diagnostic ability of ganglion cell-inner plexiform layer according to the range around the fovea
title_short Comparison of glaucoma diagnostic ability of ganglion cell-inner plexiform layer according to the range around the fovea
title_sort comparison of glaucoma diagnostic ability of ganglion cell-inner plexiform layer according to the range around the fovea
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6937720/
https://www.ncbi.nlm.nih.gov/pubmed/31888556
http://dx.doi.org/10.1186/s12886-019-1283-y
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