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Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in USH2A Retinopathy

PURPOSE: Microperimetry is commonly used to assess retinal function. We perform cross-sectional and longitudinal analysis on microperimetry parameters in USH2A retinopathy and explore end points suitable for future clinical trials. METHODS: Microperimetry was performed using two grids, Grid 1 (18° d...

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Autores principales: Charng, Jason, Lamey, Tina M., Thompson, Jennifer A., McLaren, Terri L., Attia, Mary S., McAllister, Ian L., Constable, Ian J., Mackey, David A., De Roach, John N., Chen, Fred K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488629/
https://www.ncbi.nlm.nih.gov/pubmed/32974081
http://dx.doi.org/10.1167/tvst.9.10.9
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author Charng, Jason
Lamey, Tina M.
Thompson, Jennifer A.
McLaren, Terri L.
Attia, Mary S.
McAllister, Ian L.
Constable, Ian J.
Mackey, David A.
De Roach, John N.
Chen, Fred K.
author_facet Charng, Jason
Lamey, Tina M.
Thompson, Jennifer A.
McLaren, Terri L.
Attia, Mary S.
McAllister, Ian L.
Constable, Ian J.
Mackey, David A.
De Roach, John N.
Chen, Fred K.
author_sort Charng, Jason
collection PubMed
description PURPOSE: Microperimetry is commonly used to assess retinal function. We perform cross-sectional and longitudinal analysis on microperimetry parameters in USH2A retinopathy and explore end points suitable for future clinical trials. METHODS: Microperimetry was performed using two grids, Grid 1 (18° diameter) and Grid 2 (6° diameter). In Grid 1, four parameters (number of nonscotomatous loci, mean sensitivity [MS], responding point sensitivity [RPS], and edge of scotoma sensitivity [ESS]) were analyzed. In Grid 2, number of nonscotomatous loci and MS were examined. Interocular symmetry was also examined. Longitudinal analysis was conducted in a subset of eyes. RESULTS: Microperimetry could be performed in 16 of 21 patients. In Grid 1 (n = 15; average age, 35.6 years), average number of nonscotomatous loci, MS, RPS, and ESS were 46.6 loci, 10.0 dB, 14.7 and 9.6 dB, respectively. In Grid 2 (n = 13; average age, 37.4 years), 12 eyes had measurable sensitivity across the entire grid. Average MS was 23.8 dB. Interocular analysis revealed large 95% confidence intervals for all parameters. Longitudinally, Grid 1 (n = 12, average follow-up 2.6 years) ESS showed the fastest rate of decline (–1.84 dB/y) compared with MS (–0.34 dB/y) and RPS (–0.90 dB/y). CONCLUSIONS: Our data suggest that ESS may be more useful than MS and RPS in test grids that cover a large extent of the macula. We caution the use of contralateral eye as an internal control. TRANSLATIONAL RELEVANCE: ESS may decrease the duration or sample size of treatment trials in USH2A retinopathy.
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spelling pubmed-74886292020-09-23 Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in USH2A Retinopathy Charng, Jason Lamey, Tina M. Thompson, Jennifer A. McLaren, Terri L. Attia, Mary S. McAllister, Ian L. Constable, Ian J. Mackey, David A. De Roach, John N. Chen, Fred K. Transl Vis Sci Technol Article PURPOSE: Microperimetry is commonly used to assess retinal function. We perform cross-sectional and longitudinal analysis on microperimetry parameters in USH2A retinopathy and explore end points suitable for future clinical trials. METHODS: Microperimetry was performed using two grids, Grid 1 (18° diameter) and Grid 2 (6° diameter). In Grid 1, four parameters (number of nonscotomatous loci, mean sensitivity [MS], responding point sensitivity [RPS], and edge of scotoma sensitivity [ESS]) were analyzed. In Grid 2, number of nonscotomatous loci and MS were examined. Interocular symmetry was also examined. Longitudinal analysis was conducted in a subset of eyes. RESULTS: Microperimetry could be performed in 16 of 21 patients. In Grid 1 (n = 15; average age, 35.6 years), average number of nonscotomatous loci, MS, RPS, and ESS were 46.6 loci, 10.0 dB, 14.7 and 9.6 dB, respectively. In Grid 2 (n = 13; average age, 37.4 years), 12 eyes had measurable sensitivity across the entire grid. Average MS was 23.8 dB. Interocular analysis revealed large 95% confidence intervals for all parameters. Longitudinally, Grid 1 (n = 12, average follow-up 2.6 years) ESS showed the fastest rate of decline (–1.84 dB/y) compared with MS (–0.34 dB/y) and RPS (–0.90 dB/y). CONCLUSIONS: Our data suggest that ESS may be more useful than MS and RPS in test grids that cover a large extent of the macula. We caution the use of contralateral eye as an internal control. TRANSLATIONAL RELEVANCE: ESS may decrease the duration or sample size of treatment trials in USH2A retinopathy. The Association for Research in Vision and Ophthalmology 2020-09-09 /pmc/articles/PMC7488629/ /pubmed/32974081 http://dx.doi.org/10.1167/tvst.9.10.9 Text en Copyright 2020 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 Article
Charng, Jason
Lamey, Tina M.
Thompson, Jennifer A.
McLaren, Terri L.
Attia, Mary S.
McAllister, Ian L.
Constable, Ian J.
Mackey, David A.
De Roach, John N.
Chen, Fred K.
Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in USH2A Retinopathy
title Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in USH2A Retinopathy
title_full Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in USH2A Retinopathy
title_fullStr Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in USH2A Retinopathy
title_full_unstemmed Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in USH2A Retinopathy
title_short Edge of Scotoma Sensitivity as a Microperimetry Clinical Trial End Point in USH2A Retinopathy
title_sort edge of scotoma sensitivity as a microperimetry clinical trial end point in ush2a retinopathy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7488629/
https://www.ncbi.nlm.nih.gov/pubmed/32974081
http://dx.doi.org/10.1167/tvst.9.10.9
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