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Difference in patterns of retinal ganglion cell damage between primary open-angle glaucoma and non-arteritic anterior ischaemic optic neuropathy

PURPOSE: To compare the patterns of retinal ganglion cell damage between primary open-angle glaucoma (POAG) and non-arteritic anterior ischaemic optic neuropathy (NAION). METHODS: In total, 35 eyes with unilateral NAION, and 70 age- and average peripapillary retinal nerve fibre layer (RNFL) thicknes...

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Autores principales: Lee, Yeon Hee, Kim, Kyoung Nam, Heo, Dong Won, Kang, Tae Seen, Lee, Sung Bok, Kim, Chang-sik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658149/
https://www.ncbi.nlm.nih.gov/pubmed/29073261
http://dx.doi.org/10.1371/journal.pone.0187093
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author Lee, Yeon Hee
Kim, Kyoung Nam
Heo, Dong Won
Kang, Tae Seen
Lee, Sung Bok
Kim, Chang-sik
author_facet Lee, Yeon Hee
Kim, Kyoung Nam
Heo, Dong Won
Kang, Tae Seen
Lee, Sung Bok
Kim, Chang-sik
author_sort Lee, Yeon Hee
collection PubMed
description PURPOSE: To compare the patterns of retinal ganglion cell damage between primary open-angle glaucoma (POAG) and non-arteritic anterior ischaemic optic neuropathy (NAION). METHODS: In total, 35 eyes with unilateral NAION, and 70 age- and average peripapillary retinal nerve fibre layer (RNFL) thickness-matched eyes with POAG, were enrolled as disease groups; 35 unaffected fellow eyes of the NAION, and 70 age- and refractive error-matched normal subjects for the POAG, were enrolled as their control groups, respectively. The peripapillary RNFL thickness and macular ganglion cell plus inner plexiform layer (GCIPL) thickness were compared between the disease groups and their controls, and between the two disease groups. RESULTS: Mean RNFL thicknesses at the 1 and 2 o’clock (superonasal) positions were thinner in NAION than in POAG (both p < 0.05). Mean RNFL thickness at 7 o’clock (inferotemporal) was thinner in POAG than in NAION (p = 0.001). Although there was no significant difference between NAION and POAG in average GCIPL thickness, all of the sectoral GCIPL thicknesses were thinner in NAION (all p < 0.05), except in the inferior and inferotemporal sectors. The ranges of the clock-hour RNFL with damage greater than the average RNFL thickness reduction, versus fellow eyes and control eyes, were 7 hours in NAION and 4 hours in POAG. CONCLUSIONS: The more damaged clock-hour RNFL regions differed between NAION (1 and 2 o’clock) and POAG (7 o’clock). Most sectoral GCIPL thicknesses were thinner in NAION than in POAG.
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spelling pubmed-56581492017-11-09 Difference in patterns of retinal ganglion cell damage between primary open-angle glaucoma and non-arteritic anterior ischaemic optic neuropathy Lee, Yeon Hee Kim, Kyoung Nam Heo, Dong Won Kang, Tae Seen Lee, Sung Bok Kim, Chang-sik PLoS One Research Article PURPOSE: To compare the patterns of retinal ganglion cell damage between primary open-angle glaucoma (POAG) and non-arteritic anterior ischaemic optic neuropathy (NAION). METHODS: In total, 35 eyes with unilateral NAION, and 70 age- and average peripapillary retinal nerve fibre layer (RNFL) thickness-matched eyes with POAG, were enrolled as disease groups; 35 unaffected fellow eyes of the NAION, and 70 age- and refractive error-matched normal subjects for the POAG, were enrolled as their control groups, respectively. The peripapillary RNFL thickness and macular ganglion cell plus inner plexiform layer (GCIPL) thickness were compared between the disease groups and their controls, and between the two disease groups. RESULTS: Mean RNFL thicknesses at the 1 and 2 o’clock (superonasal) positions were thinner in NAION than in POAG (both p < 0.05). Mean RNFL thickness at 7 o’clock (inferotemporal) was thinner in POAG than in NAION (p = 0.001). Although there was no significant difference between NAION and POAG in average GCIPL thickness, all of the sectoral GCIPL thicknesses were thinner in NAION (all p < 0.05), except in the inferior and inferotemporal sectors. The ranges of the clock-hour RNFL with damage greater than the average RNFL thickness reduction, versus fellow eyes and control eyes, were 7 hours in NAION and 4 hours in POAG. CONCLUSIONS: The more damaged clock-hour RNFL regions differed between NAION (1 and 2 o’clock) and POAG (7 o’clock). Most sectoral GCIPL thicknesses were thinner in NAION than in POAG. Public Library of Science 2017-10-26 /pmc/articles/PMC5658149/ /pubmed/29073261 http://dx.doi.org/10.1371/journal.pone.0187093 Text en © 2017 Lee et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lee, Yeon Hee
Kim, Kyoung Nam
Heo, Dong Won
Kang, Tae Seen
Lee, Sung Bok
Kim, Chang-sik
Difference in patterns of retinal ganglion cell damage between primary open-angle glaucoma and non-arteritic anterior ischaemic optic neuropathy
title Difference in patterns of retinal ganglion cell damage between primary open-angle glaucoma and non-arteritic anterior ischaemic optic neuropathy
title_full Difference in patterns of retinal ganglion cell damage between primary open-angle glaucoma and non-arteritic anterior ischaemic optic neuropathy
title_fullStr Difference in patterns of retinal ganglion cell damage between primary open-angle glaucoma and non-arteritic anterior ischaemic optic neuropathy
title_full_unstemmed Difference in patterns of retinal ganglion cell damage between primary open-angle glaucoma and non-arteritic anterior ischaemic optic neuropathy
title_short Difference in patterns of retinal ganglion cell damage between primary open-angle glaucoma and non-arteritic anterior ischaemic optic neuropathy
title_sort difference in patterns of retinal ganglion cell damage between primary open-angle glaucoma and non-arteritic anterior ischaemic optic neuropathy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658149/
https://www.ncbi.nlm.nih.gov/pubmed/29073261
http://dx.doi.org/10.1371/journal.pone.0187093
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