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Spatial Characteristics of Peripheral Visual Islands in Retinitis Pigmentosa
PURPOSE: Retinitis pigmentosa (RP) is typified by progressive peripheral visual field (pVF) loss in patterns that can vary between individuals. Greater understanding of pVF preservation may inform research on therapeutic targets. However, characteristics of retained pVF are incompletely understood....
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857617/ https://www.ncbi.nlm.nih.gov/pubmed/35175279 http://dx.doi.org/10.1167/iovs.63.2.26 |
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author | Patel, Tapan P. Vongsachang, Hursuong Schilling, Andrew Kong, Xiangrong Singh, Mandeep S. |
author_facet | Patel, Tapan P. Vongsachang, Hursuong Schilling, Andrew Kong, Xiangrong Singh, Mandeep S. |
author_sort | Patel, Tapan P. |
collection | PubMed |
description | PURPOSE: Retinitis pigmentosa (RP) is typified by progressive peripheral visual field (pVF) loss in patterns that can vary between individuals. Greater understanding of pVF preservation may inform research on therapeutic targets. However, characteristics of retained pVF are incompletely understood. We aimed to evaluate the spatial characteristics of retained pVF in RP. METHODS: We developed a computational platform to generate a probability map of the spatial distribution of retained pVF loci using the Goldmann V4e isopter. RP subjects were grouped into cross-sectional and longitudinal datasets. Probability maps of retained pVF were generated for categories of symptomatic disease duration (SDD). We applied a mathematical model to determine the anatomical correlate of the retained pVF. RESULTS: A total of 152 subjects were included. The mean age was 46.7 years. SDD was <20 years (47.4%), 20 to 40 years (39.5%), or >40 years (13.2%). Longitudinal data (3.2–5.7 years of follow up) were available for 65 subjects. In the cross-sectional dataset, retained pVF loci were most likely to be located between the 50° and 80° isoeccentric meridians and between the 30° to 50° radial axes. In the longitudinal dataset, inferotemporal pVF loci were the most likely to be preserved over time. The area of pVF retention corresponded anatomically to the pre-equatorial superonasal retina. CONCLUSIONS: Semiautomated quantitation of pVF may be a useful tool to analyze spatial characteristics of VF in RP. Retinal cells in the superonasal periphery may be resilient to RP-related functional decline. Understanding the cellular and molecular basis of pVF resilience in the retina may inform efforts to develop treatment modalities for RP. |
format | Online Article Text |
id | pubmed-8857617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Association for Research in Vision and Ophthalmology |
record_format | MEDLINE/PubMed |
spelling | pubmed-88576172022-02-20 Spatial Characteristics of Peripheral Visual Islands in Retinitis Pigmentosa Patel, Tapan P. Vongsachang, Hursuong Schilling, Andrew Kong, Xiangrong Singh, Mandeep S. Invest Ophthalmol Vis Sci Retina PURPOSE: Retinitis pigmentosa (RP) is typified by progressive peripheral visual field (pVF) loss in patterns that can vary between individuals. Greater understanding of pVF preservation may inform research on therapeutic targets. However, characteristics of retained pVF are incompletely understood. We aimed to evaluate the spatial characteristics of retained pVF in RP. METHODS: We developed a computational platform to generate a probability map of the spatial distribution of retained pVF loci using the Goldmann V4e isopter. RP subjects were grouped into cross-sectional and longitudinal datasets. Probability maps of retained pVF were generated for categories of symptomatic disease duration (SDD). We applied a mathematical model to determine the anatomical correlate of the retained pVF. RESULTS: A total of 152 subjects were included. The mean age was 46.7 years. SDD was <20 years (47.4%), 20 to 40 years (39.5%), or >40 years (13.2%). Longitudinal data (3.2–5.7 years of follow up) were available for 65 subjects. In the cross-sectional dataset, retained pVF loci were most likely to be located between the 50° and 80° isoeccentric meridians and between the 30° to 50° radial axes. In the longitudinal dataset, inferotemporal pVF loci were the most likely to be preserved over time. The area of pVF retention corresponded anatomically to the pre-equatorial superonasal retina. CONCLUSIONS: Semiautomated quantitation of pVF may be a useful tool to analyze spatial characteristics of VF in RP. Retinal cells in the superonasal periphery may be resilient to RP-related functional decline. Understanding the cellular and molecular basis of pVF resilience in the retina may inform efforts to develop treatment modalities for RP. The Association for Research in Vision and Ophthalmology 2022-02-17 /pmc/articles/PMC8857617/ /pubmed/35175279 http://dx.doi.org/10.1167/iovs.63.2.26 Text en Copyright 2022 The Authors https://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 Patel, Tapan P. Vongsachang, Hursuong Schilling, Andrew Kong, Xiangrong Singh, Mandeep S. Spatial Characteristics of Peripheral Visual Islands in Retinitis Pigmentosa |
title | Spatial Characteristics of Peripheral Visual Islands in Retinitis Pigmentosa |
title_full | Spatial Characteristics of Peripheral Visual Islands in Retinitis Pigmentosa |
title_fullStr | Spatial Characteristics of Peripheral Visual Islands in Retinitis Pigmentosa |
title_full_unstemmed | Spatial Characteristics of Peripheral Visual Islands in Retinitis Pigmentosa |
title_short | Spatial Characteristics of Peripheral Visual Islands in Retinitis Pigmentosa |
title_sort | spatial characteristics of peripheral visual islands in retinitis pigmentosa |
topic | Retina |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857617/ https://www.ncbi.nlm.nih.gov/pubmed/35175279 http://dx.doi.org/10.1167/iovs.63.2.26 |
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