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Associations Between Retinal Pigment Epithelium and Drusen Volume Changes During the Lifecycle of Large Drusenoid Pigment Epithelial Detachments

PURPOSE: Drusenoid pigment epithelial detachments (PEDs) are a defined path to atrophy in age-related macular degeneration (AMD). We analyzed the relationships between retinal pigment epithelium (RPE) and drusen volume changes during the PED lifecycle, using spectral-domain optical coherence tomogra...

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Autores principales: Balaratnasingam, Chandrakumar, Yannuzzi, Lawrence A., Curcio, Christine A., Morgan, William H., Querques, Giuseppe, Capuano, Vittorio, Souied, Eric, Jung, Jesse, Freund, K. Bailey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072538/
https://www.ncbi.nlm.nih.gov/pubmed/27760262
http://dx.doi.org/10.1167/iovs.16-19816
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author Balaratnasingam, Chandrakumar
Yannuzzi, Lawrence A.
Curcio, Christine A.
Morgan, William H.
Querques, Giuseppe
Capuano, Vittorio
Souied, Eric
Jung, Jesse
Freund, K. Bailey
author_facet Balaratnasingam, Chandrakumar
Yannuzzi, Lawrence A.
Curcio, Christine A.
Morgan, William H.
Querques, Giuseppe
Capuano, Vittorio
Souied, Eric
Jung, Jesse
Freund, K. Bailey
author_sort Balaratnasingam, Chandrakumar
collection PubMed
description PURPOSE: Drusenoid pigment epithelial detachments (PEDs) are a defined path to atrophy in age-related macular degeneration (AMD). We analyzed the relationships between retinal pigment epithelium (RPE) and drusen volume changes during the PED lifecycle, using spectral-domain optical coherence tomography (SD-OCT). METHODS: Twenty-one cases of drusenoid PED tracked using SD-OCT through periods of growth and collapse were evaluated. Volumetric calculations and piece-wise linear regression analysis were used to determine the breakpoint between growth and collapse. Spectral-domain OCT scans were independently evaluated for the appearance of intraretinal hyperreflective foci, acquired vitelliform lesions (AVLs), and disruptions to the RPE+basal lamina band. Timing of these events with respect to the breakpoint was statistically evaluated. Morphometric characteristics of drusenoid PEDs were correlated with rate of PED collapse and final visual acuity. RESULTS: Mean age of subjects was 75.3 years and mean period of follow up was 4.1 years (median 4.5 years; range, 0.6–6.6 years). The lifecycle of drusenoid PEDs was asymmetric, in that the rate of collapse (0.199 mm(3)/month) is significantly faster (P < 0.001) than the rate of growth (0.022 mm(3)/month). Appearance of intraretinal hyperreflective foci and AVLs preceded the breakpoint (both P < 0.001). The timing of disruptions to the RPE+basal lamina band did not differ from the breakpoint (P = 0.510). Maximal height, volume, and diameter of drusenoid PEDs were inversely correlated with final visual acuity (all P < 0.001) and positively correlated with the rate of PED collapse (all P < 0.001). CONCLUSIONS: Spectral-domain OCT signatures, plausibly attributable to anteriorly migrated RPE and disintegration of the RPE layer, precede or occur simultaneously with changes in volume of drusenoid PED during the lifecycle of this lesion.
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spelling pubmed-50725382016-10-27 Associations Between Retinal Pigment Epithelium and Drusen Volume Changes During the Lifecycle of Large Drusenoid Pigment Epithelial Detachments Balaratnasingam, Chandrakumar Yannuzzi, Lawrence A. Curcio, Christine A. Morgan, William H. Querques, Giuseppe Capuano, Vittorio Souied, Eric Jung, Jesse Freund, K. Bailey Invest Ophthalmol Vis Sci Retina PURPOSE: Drusenoid pigment epithelial detachments (PEDs) are a defined path to atrophy in age-related macular degeneration (AMD). We analyzed the relationships between retinal pigment epithelium (RPE) and drusen volume changes during the PED lifecycle, using spectral-domain optical coherence tomography (SD-OCT). METHODS: Twenty-one cases of drusenoid PED tracked using SD-OCT through periods of growth and collapse were evaluated. Volumetric calculations and piece-wise linear regression analysis were used to determine the breakpoint between growth and collapse. Spectral-domain OCT scans were independently evaluated for the appearance of intraretinal hyperreflective foci, acquired vitelliform lesions (AVLs), and disruptions to the RPE+basal lamina band. Timing of these events with respect to the breakpoint was statistically evaluated. Morphometric characteristics of drusenoid PEDs were correlated with rate of PED collapse and final visual acuity. RESULTS: Mean age of subjects was 75.3 years and mean period of follow up was 4.1 years (median 4.5 years; range, 0.6–6.6 years). The lifecycle of drusenoid PEDs was asymmetric, in that the rate of collapse (0.199 mm(3)/month) is significantly faster (P < 0.001) than the rate of growth (0.022 mm(3)/month). Appearance of intraretinal hyperreflective foci and AVLs preceded the breakpoint (both P < 0.001). The timing of disruptions to the RPE+basal lamina band did not differ from the breakpoint (P = 0.510). Maximal height, volume, and diameter of drusenoid PEDs were inversely correlated with final visual acuity (all P < 0.001) and positively correlated with the rate of PED collapse (all P < 0.001). CONCLUSIONS: Spectral-domain OCT signatures, plausibly attributable to anteriorly migrated RPE and disintegration of the RPE layer, precede or occur simultaneously with changes in volume of drusenoid PED during the lifecycle of this lesion. The Association for Research in Vision and Ophthalmology 2016-10 /pmc/articles/PMC5072538/ /pubmed/27760262 http://dx.doi.org/10.1167/iovs.16-19816 Text en 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 Retina
Balaratnasingam, Chandrakumar
Yannuzzi, Lawrence A.
Curcio, Christine A.
Morgan, William H.
Querques, Giuseppe
Capuano, Vittorio
Souied, Eric
Jung, Jesse
Freund, K. Bailey
Associations Between Retinal Pigment Epithelium and Drusen Volume Changes During the Lifecycle of Large Drusenoid Pigment Epithelial Detachments
title Associations Between Retinal Pigment Epithelium and Drusen Volume Changes During the Lifecycle of Large Drusenoid Pigment Epithelial Detachments
title_full Associations Between Retinal Pigment Epithelium and Drusen Volume Changes During the Lifecycle of Large Drusenoid Pigment Epithelial Detachments
title_fullStr Associations Between Retinal Pigment Epithelium and Drusen Volume Changes During the Lifecycle of Large Drusenoid Pigment Epithelial Detachments
title_full_unstemmed Associations Between Retinal Pigment Epithelium and Drusen Volume Changes During the Lifecycle of Large Drusenoid Pigment Epithelial Detachments
title_short Associations Between Retinal Pigment Epithelium and Drusen Volume Changes During the Lifecycle of Large Drusenoid Pigment Epithelial Detachments
title_sort associations between retinal pigment epithelium and drusen volume changes during the lifecycle of large drusenoid pigment epithelial detachments
topic Retina
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072538/
https://www.ncbi.nlm.nih.gov/pubmed/27760262
http://dx.doi.org/10.1167/iovs.16-19816
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