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Quantification of Retinal Ganglion Cell Morphology in Human Glaucomatous Eyes

PURPOSE: To characterize retinal ganglion cell morphological changes in patients with primary open-angle glaucoma associated with hemifield defect (HD) using adaptive optics–optical coherence tomography (AO-OCT). METHODS: Six patients with early to moderate primary open-angle glaucoma with an averag...

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Autores principales: Liu, Zhuolin, Saeedi, Osamah, Zhang, Furu, Villanueva, Ricardo, Asanad, Samuel, Agrawal, Anant, Hammer, Daniel X.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995922/
https://www.ncbi.nlm.nih.gov/pubmed/33760041
http://dx.doi.org/10.1167/iovs.62.3.34
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author Liu, Zhuolin
Saeedi, Osamah
Zhang, Furu
Villanueva, Ricardo
Asanad, Samuel
Agrawal, Anant
Hammer, Daniel X.
author_facet Liu, Zhuolin
Saeedi, Osamah
Zhang, Furu
Villanueva, Ricardo
Asanad, Samuel
Agrawal, Anant
Hammer, Daniel X.
author_sort Liu, Zhuolin
collection PubMed
description PURPOSE: To characterize retinal ganglion cell morphological changes in patients with primary open-angle glaucoma associated with hemifield defect (HD) using adaptive optics–optical coherence tomography (AO-OCT). METHODS: Six patients with early to moderate primary open-angle glaucoma with an average age of 58 years associated with HD and six age-matched healthy controls with an average age of 61 years were included. All participants underwent in vivo retinal ganglion cell (RGC) imaging at six primary locations across the macula with AO-OCT. Ganglion cell layer (GCL) somas were manually counted, and morphological parameters of GCL soma density, size, and symmetry were calculated. RGC cellular characteristics were correlated with functional visual field measurements. RESULTS: GCL soma density was 12,799 ± 7747 cells/mm(2), 9370 ± 5572 cells/mm(2), and 2134 ± 1494 cells/mm(2) at 3°, 6°, and 12°, respectively, in glaucoma patients compared with 25,058 ± 4649 cells/mm(2), 15,551 ± 2301 cells/mm(2), and 3891 ± 1105 cells/mm(2) (P < 0.05 for all locations) at the corresponding retinal locations in healthy participants. Mean soma diameter was significantly larger in glaucoma patients (14.20 ± 2.30 µm) compared with the health controls (12.32 ± 1.94 µm, P < 0.05 for all locations); symmetry was 0.36 ± 0.32 and 0.86 ± 0.13 in glaucoma and control cohorts, respectively. CONCLUSIONS: Glaucoma patients had lower GCL soma density and symmetry, greater soma size, and increased variation of GCL soma reflectance compared with age-matched control subjects. The morphological changes corresponded with HD, and the cellular level structural loss correlated with visual function loss in glaucoma. AO-based morphological parameters could be potential sensitive biomarkers for glaucoma.
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spelling pubmed-79959222021-04-01 Quantification of Retinal Ganglion Cell Morphology in Human Glaucomatous Eyes Liu, Zhuolin Saeedi, Osamah Zhang, Furu Villanueva, Ricardo Asanad, Samuel Agrawal, Anant Hammer, Daniel X. Invest Ophthalmol Vis Sci Multidisciplinary Ophthalmic Imaging PURPOSE: To characterize retinal ganglion cell morphological changes in patients with primary open-angle glaucoma associated with hemifield defect (HD) using adaptive optics–optical coherence tomography (AO-OCT). METHODS: Six patients with early to moderate primary open-angle glaucoma with an average age of 58 years associated with HD and six age-matched healthy controls with an average age of 61 years were included. All participants underwent in vivo retinal ganglion cell (RGC) imaging at six primary locations across the macula with AO-OCT. Ganglion cell layer (GCL) somas were manually counted, and morphological parameters of GCL soma density, size, and symmetry were calculated. RGC cellular characteristics were correlated with functional visual field measurements. RESULTS: GCL soma density was 12,799 ± 7747 cells/mm(2), 9370 ± 5572 cells/mm(2), and 2134 ± 1494 cells/mm(2) at 3°, 6°, and 12°, respectively, in glaucoma patients compared with 25,058 ± 4649 cells/mm(2), 15,551 ± 2301 cells/mm(2), and 3891 ± 1105 cells/mm(2) (P < 0.05 for all locations) at the corresponding retinal locations in healthy participants. Mean soma diameter was significantly larger in glaucoma patients (14.20 ± 2.30 µm) compared with the health controls (12.32 ± 1.94 µm, P < 0.05 for all locations); symmetry was 0.36 ± 0.32 and 0.86 ± 0.13 in glaucoma and control cohorts, respectively. CONCLUSIONS: Glaucoma patients had lower GCL soma density and symmetry, greater soma size, and increased variation of GCL soma reflectance compared with age-matched control subjects. The morphological changes corresponded with HD, and the cellular level structural loss correlated with visual function loss in glaucoma. AO-based morphological parameters could be potential sensitive biomarkers for glaucoma. The Association for Research in Vision and Ophthalmology 2021-03-24 /pmc/articles/PMC7995922/ /pubmed/33760041 http://dx.doi.org/10.1167/iovs.62.3.34 Text en Copyright 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
spellingShingle Multidisciplinary Ophthalmic Imaging
Liu, Zhuolin
Saeedi, Osamah
Zhang, Furu
Villanueva, Ricardo
Asanad, Samuel
Agrawal, Anant
Hammer, Daniel X.
Quantification of Retinal Ganglion Cell Morphology in Human Glaucomatous Eyes
title Quantification of Retinal Ganglion Cell Morphology in Human Glaucomatous Eyes
title_full Quantification of Retinal Ganglion Cell Morphology in Human Glaucomatous Eyes
title_fullStr Quantification of Retinal Ganglion Cell Morphology in Human Glaucomatous Eyes
title_full_unstemmed Quantification of Retinal Ganglion Cell Morphology in Human Glaucomatous Eyes
title_short Quantification of Retinal Ganglion Cell Morphology in Human Glaucomatous Eyes
title_sort quantification of retinal ganglion cell morphology in human glaucomatous eyes
topic Multidisciplinary Ophthalmic Imaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995922/
https://www.ncbi.nlm.nih.gov/pubmed/33760041
http://dx.doi.org/10.1167/iovs.62.3.34
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