Analysis of Peripapillary Atrophy Using Spectral Domain Optical Coherence Tomography

Objective To study retinal morphologic changes around the optic disc in patients with peripapillary atrophy (PPA) with high-resolution spectral domain optical coherence tomography (SD OCT). Design Cross-sectional, retrospective analysis. Participants A total of 103 eyes of 73 patients with PPA...

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Main Authors: Manjunath, Varsha, Shah, Heeral, Fujimoto, James G., Duker, Jay S.
Other Authors: Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
Format: Article
Language:en_US
Published: Elsevier 2015
Online Access:http://hdl.handle.net/1721.1/98863
https://orcid.org/0000-0002-0828-4357
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author Manjunath, Varsha
Shah, Heeral
Fujimoto, James G.
Duker, Jay S.
author2 Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
author_facet Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science
Manjunath, Varsha
Shah, Heeral
Fujimoto, James G.
Duker, Jay S.
author_sort Manjunath, Varsha
collection MIT
description Objective To study retinal morphologic changes around the optic disc in patients with peripapillary atrophy (PPA) with high-resolution spectral domain optical coherence tomography (SD OCT). Design Cross-sectional, retrospective analysis. Participants A total of 103 eyes of 73 patients with PPA and 21 eyes of 12 normal patients seen at the New England Eye Center, Tufts Medical Center, between January 2007 and August 2009. Methods Spectral domain optical coherence tomography images taken through the region of PPA were quantitatively and qualitatively analyzed. Inclusion criteria included eyes with at least 300 μm of temporal PPA as detected on color fundus photographs. The study population was divided into subgroups according to the following clinical diagnoses: glaucoma (n=13), age-related macular degeneration (n=11), high myopia (n=11), glaucoma and high myopia (n=3), and optic neuropathy (n=11). Fifty-four patients were classified with other diagnoses. By using OCT software, retinal thickness and retinal nerve fiber layer (RNFL) thickness were both manually measured perpendicular to the internal limiting membrane and retinal pigment epithelium (RPE) 300 μm temporal to the optic disc, within the region of PPA. Qualitative analysis for morphologic changes in the atrophic area was also performed. Main Outcome Measures Qualitative assessment and quantitative measures of retinal and RNFL thickness in PPA. Results The study group was categorized by 6 characteristics demonstrated in the area of PPA by SD OCT: RPE loss with accompanying photoreceptor loss, RPE disruption, RNFL thickening with plaque-like formation, intraretinal cystic changes, inner and outer retinal thinning, and abnormal retinal sloping. Statistical analysis of measurements revealed a statistically significant difference in the total retinal thickness between normal eyes and eyes with PPA (P=0.0005), with normal eyes 15% thicker than the eyes with PPA; however, the RNFL thickness was not significantly different between the normal eyes and the eyes with PPA (P=0.05). Conclusions Eyes with PPA manifest characteristic retinal changes that can be described via SD OCT.
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spelling mit-1721.1/988632022-10-01T04:58:47Z Analysis of Peripapillary Atrophy Using Spectral Domain Optical Coherence Tomography Manjunath, Varsha Shah, Heeral Fujimoto, James G. Duker, Jay S. Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science Massachusetts Institute of Technology. Research Laboratory of Electronics Fujimoto, James G. Objective To study retinal morphologic changes around the optic disc in patients with peripapillary atrophy (PPA) with high-resolution spectral domain optical coherence tomography (SD OCT). Design Cross-sectional, retrospective analysis. Participants A total of 103 eyes of 73 patients with PPA and 21 eyes of 12 normal patients seen at the New England Eye Center, Tufts Medical Center, between January 2007 and August 2009. Methods Spectral domain optical coherence tomography images taken through the region of PPA were quantitatively and qualitatively analyzed. Inclusion criteria included eyes with at least 300 μm of temporal PPA as detected on color fundus photographs. The study population was divided into subgroups according to the following clinical diagnoses: glaucoma (n=13), age-related macular degeneration (n=11), high myopia (n=11), glaucoma and high myopia (n=3), and optic neuropathy (n=11). Fifty-four patients were classified with other diagnoses. By using OCT software, retinal thickness and retinal nerve fiber layer (RNFL) thickness were both manually measured perpendicular to the internal limiting membrane and retinal pigment epithelium (RPE) 300 μm temporal to the optic disc, within the region of PPA. Qualitative analysis for morphologic changes in the atrophic area was also performed. Main Outcome Measures Qualitative assessment and quantitative measures of retinal and RNFL thickness in PPA. Results The study group was categorized by 6 characteristics demonstrated in the area of PPA by SD OCT: RPE loss with accompanying photoreceptor loss, RPE disruption, RNFL thickening with plaque-like formation, intraretinal cystic changes, inner and outer retinal thinning, and abnormal retinal sloping. Statistical analysis of measurements revealed a statistically significant difference in the total retinal thickness between normal eyes and eyes with PPA (P=0.0005), with normal eyes 15% thicker than the eyes with PPA; however, the RNFL thickness was not significantly different between the normal eyes and the eyes with PPA (P=0.05). Conclusions Eyes with PPA manifest characteristic retinal changes that can be described via SD OCT. National Institutes of Health (U.S.) (Contract R01-EY11289-24) National Institutes of Health (U.S.) (Contract R01-EY13178-10) National Institutes of Health (U.S.) (Contract R01-EY013516-07) United States. Air Force Office of Scientific Research (FA9550-07-1-0101) United States. Air Force Office of Scientific Research (FA9550-07-1-0014) Massachusetts Lions Eye Research Fund, Inc. 2015-09-22T17:11:06Z 2015-09-22T17:11:06Z 2010-10 2010-06 Article http://purl.org/eprint/type/JournalArticle 01616420 http://hdl.handle.net/1721.1/98863 Manjunath, Varsha, Heeral Shah, James G. Fujimoto, and Jay S. Duker. “Analysis of Peripapillary Atrophy Using Spectral Domain Optical Coherence Tomography.” Ophthalmology 118, no. 3 (March 2011): 531–536. https://orcid.org/0000-0002-0828-4357 en_US http://dx.doi.org/10.1016/j.ophtha.2010.07.013 Ophthalmology Creative Commons Attribution-Noncommercial-NoDerivatives http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Elsevier PMC
spellingShingle Manjunath, Varsha
Shah, Heeral
Fujimoto, James G.
Duker, Jay S.
Analysis of Peripapillary Atrophy Using Spectral Domain Optical Coherence Tomography
title Analysis of Peripapillary Atrophy Using Spectral Domain Optical Coherence Tomography
title_full Analysis of Peripapillary Atrophy Using Spectral Domain Optical Coherence Tomography
title_fullStr Analysis of Peripapillary Atrophy Using Spectral Domain Optical Coherence Tomography
title_full_unstemmed Analysis of Peripapillary Atrophy Using Spectral Domain Optical Coherence Tomography
title_short Analysis of Peripapillary Atrophy Using Spectral Domain Optical Coherence Tomography
title_sort analysis of peripapillary atrophy using spectral domain optical coherence tomography
url http://hdl.handle.net/1721.1/98863
https://orcid.org/0000-0002-0828-4357
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