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Modeling absolute zone size in retinopathy of prematurity in relation to axial length

Treatment outcomes in retinopathy of prematurity (ROP) are closely correlated with the location (i.e. zone) of disease, with more posterior zones having poorer outcomes. The most posterior zone, Zone I, is defined as a circle centered on the optic nerve with radius twice the distance from nerve to f...

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Autores principales: Wang, Sean K., Korot, Edward, Zaidi, Moosa, Ji, Marco H., Al-Moujahed, Ahmad, Callaway, Natalia F., Kumm, Jochen, Moshfeghi, Darius M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933429/
https://www.ncbi.nlm.nih.gov/pubmed/35304549
http://dx.doi.org/10.1038/s41598-022-08680-5
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author Wang, Sean K.
Korot, Edward
Zaidi, Moosa
Ji, Marco H.
Al-Moujahed, Ahmad
Callaway, Natalia F.
Kumm, Jochen
Moshfeghi, Darius M.
author_facet Wang, Sean K.
Korot, Edward
Zaidi, Moosa
Ji, Marco H.
Al-Moujahed, Ahmad
Callaway, Natalia F.
Kumm, Jochen
Moshfeghi, Darius M.
author_sort Wang, Sean K.
collection PubMed
description Treatment outcomes in retinopathy of prematurity (ROP) are closely correlated with the location (i.e. zone) of disease, with more posterior zones having poorer outcomes. The most posterior zone, Zone I, is defined as a circle centered on the optic nerve with radius twice the distance from nerve to fovea, or subtending an angle of 30 degrees. Because the eye enlarges and undergoes refractive changes during the period of ROP screening, the absolute area of Zone I according to these definitions may likewise change. It is possible that these differences may confound accurate assessment of risk in patients with ROP. In this study, we estimated the area of Zone I in relation to different ocular parameters to determine how variability in the size and refractive power of the eye may affect zoning. Using Gaussian optics, a model was constructed to calculate the absolute area of Zone I as a function of corneal power, anterior chamber depth, lens power, lens thickness, and axial length (AL), with Zone I defined as a circle with radius set by a 30-degree visual angle. Our model predicted Zone I area to be most sensitive to changes in AL; for example, an increase of AL from 14.20 to 16.58 mm at postmenstrual age 32 weeks was calculated to expand the area of Zone I by up to 72%. These findings motivate several hypotheses which upon future testing may help optimize treatment decisions for ROP.
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spelling pubmed-89334292022-03-28 Modeling absolute zone size in retinopathy of prematurity in relation to axial length Wang, Sean K. Korot, Edward Zaidi, Moosa Ji, Marco H. Al-Moujahed, Ahmad Callaway, Natalia F. Kumm, Jochen Moshfeghi, Darius M. Sci Rep Article Treatment outcomes in retinopathy of prematurity (ROP) are closely correlated with the location (i.e. zone) of disease, with more posterior zones having poorer outcomes. The most posterior zone, Zone I, is defined as a circle centered on the optic nerve with radius twice the distance from nerve to fovea, or subtending an angle of 30 degrees. Because the eye enlarges and undergoes refractive changes during the period of ROP screening, the absolute area of Zone I according to these definitions may likewise change. It is possible that these differences may confound accurate assessment of risk in patients with ROP. In this study, we estimated the area of Zone I in relation to different ocular parameters to determine how variability in the size and refractive power of the eye may affect zoning. Using Gaussian optics, a model was constructed to calculate the absolute area of Zone I as a function of corneal power, anterior chamber depth, lens power, lens thickness, and axial length (AL), with Zone I defined as a circle with radius set by a 30-degree visual angle. Our model predicted Zone I area to be most sensitive to changes in AL; for example, an increase of AL from 14.20 to 16.58 mm at postmenstrual age 32 weeks was calculated to expand the area of Zone I by up to 72%. These findings motivate several hypotheses which upon future testing may help optimize treatment decisions for ROP. Nature Publishing Group UK 2022-03-18 /pmc/articles/PMC8933429/ /pubmed/35304549 http://dx.doi.org/10.1038/s41598-022-08680-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Sean K.
Korot, Edward
Zaidi, Moosa
Ji, Marco H.
Al-Moujahed, Ahmad
Callaway, Natalia F.
Kumm, Jochen
Moshfeghi, Darius M.
Modeling absolute zone size in retinopathy of prematurity in relation to axial length
title Modeling absolute zone size in retinopathy of prematurity in relation to axial length
title_full Modeling absolute zone size in retinopathy of prematurity in relation to axial length
title_fullStr Modeling absolute zone size in retinopathy of prematurity in relation to axial length
title_full_unstemmed Modeling absolute zone size in retinopathy of prematurity in relation to axial length
title_short Modeling absolute zone size in retinopathy of prematurity in relation to axial length
title_sort modeling absolute zone size in retinopathy of prematurity in relation to axial length
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933429/
https://www.ncbi.nlm.nih.gov/pubmed/35304549
http://dx.doi.org/10.1038/s41598-022-08680-5
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