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Clinical Characteristics of Highly Myopic Patients With Asymmetric Myopic Atrophic Maculopathy–Analysis Using Multimodal Imaging

PURPOSE: To evaluate the factors associated with asymmetric myopic atrophic maculopathy (MAM) in highly myopic patients. METHODS: We enrolled highly myopic patients with asymmetric MAM according to the atrophy, traction, and neovascularization (ATN) classification. The results of color fundus photog...

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Autores principales: Hsia, Yun, Wang, Shih-Wen, Huang, Chien-Jung, Hung, Kuo-Chi, Chen, Muh-Shy, Ho, Tzyy-Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980047/
https://www.ncbi.nlm.nih.gov/pubmed/33724293
http://dx.doi.org/10.1167/iovs.62.3.21
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author Hsia, Yun
Wang, Shih-Wen
Huang, Chien-Jung
Hung, Kuo-Chi
Chen, Muh-Shy
Ho, Tzyy-Chang
author_facet Hsia, Yun
Wang, Shih-Wen
Huang, Chien-Jung
Hung, Kuo-Chi
Chen, Muh-Shy
Ho, Tzyy-Chang
author_sort Hsia, Yun
collection PubMed
description PURPOSE: To evaluate the factors associated with asymmetric myopic atrophic maculopathy (MAM) in highly myopic patients. METHODS: We enrolled highly myopic patients with asymmetric MAM according to the atrophy, traction, and neovascularization (ATN) classification. The results of color fundus photography, optical coherence tomography (OCT), OCT angiography, and corneal visualization Scheimpflug technology (Corvis ST tonometry) were reviewed. The association between inter-eye differences in clinical features and MAM grading was analyzed using logistic regression analysis. RESULTS: Among the 72 eyes of 36 patients 61.0 ± 9.3 years of age, 9, 33, 17, and 13 eyes had A1, A2, A3, and A4, respectively. The mean axial length was 30.44 ± 1.92 mm, and there was no significant difference between eyes with less severe and more severe MAM. The inter-eye differences in MAM grading were associated with the inter-eye differences in the presence of Bruch's membrane defects (P = 0.014), ellipsoid zone disruption (P = 0.013), vessel density of the deep retinal layer (P = 0.022), foveal avascular zone circularity (P = 0.012), foveal avascular zone area (P = 0.049), flow area of the choriocapillaris (P = 0.013), vessel diameter (P = 0.045), and fractal dimension (P = 0.015). No Corvis ST parameter was statistically significant. A higher difference in the choriocapillaris flow area (P = 0.013; adjusted odds ratio = 1.10 [1.02–1.18]) remained associated with higher inter-eye differences in MAM grading in the multivariable regression. CONCLUSIONS: A smaller choriocapillaris flow area was associated with more severe MAM, suggesting that vascular factors play pivotal roles in MAM.
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spelling pubmed-79800472021-03-26 Clinical Characteristics of Highly Myopic Patients With Asymmetric Myopic Atrophic Maculopathy–Analysis Using Multimodal Imaging Hsia, Yun Wang, Shih-Wen Huang, Chien-Jung Hung, Kuo-Chi Chen, Muh-Shy Ho, Tzyy-Chang Invest Ophthalmol Vis Sci Retina PURPOSE: To evaluate the factors associated with asymmetric myopic atrophic maculopathy (MAM) in highly myopic patients. METHODS: We enrolled highly myopic patients with asymmetric MAM according to the atrophy, traction, and neovascularization (ATN) classification. The results of color fundus photography, optical coherence tomography (OCT), OCT angiography, and corneal visualization Scheimpflug technology (Corvis ST tonometry) were reviewed. The association between inter-eye differences in clinical features and MAM grading was analyzed using logistic regression analysis. RESULTS: Among the 72 eyes of 36 patients 61.0 ± 9.3 years of age, 9, 33, 17, and 13 eyes had A1, A2, A3, and A4, respectively. The mean axial length was 30.44 ± 1.92 mm, and there was no significant difference between eyes with less severe and more severe MAM. The inter-eye differences in MAM grading were associated with the inter-eye differences in the presence of Bruch's membrane defects (P = 0.014), ellipsoid zone disruption (P = 0.013), vessel density of the deep retinal layer (P = 0.022), foveal avascular zone circularity (P = 0.012), foveal avascular zone area (P = 0.049), flow area of the choriocapillaris (P = 0.013), vessel diameter (P = 0.045), and fractal dimension (P = 0.015). No Corvis ST parameter was statistically significant. A higher difference in the choriocapillaris flow area (P = 0.013; adjusted odds ratio = 1.10 [1.02–1.18]) remained associated with higher inter-eye differences in MAM grading in the multivariable regression. CONCLUSIONS: A smaller choriocapillaris flow area was associated with more severe MAM, suggesting that vascular factors play pivotal roles in MAM. The Association for Research in Vision and Ophthalmology 2021-03-16 /pmc/articles/PMC7980047/ /pubmed/33724293 http://dx.doi.org/10.1167/iovs.62.3.21 Text en Copyright 2021 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 Retina
Hsia, Yun
Wang, Shih-Wen
Huang, Chien-Jung
Hung, Kuo-Chi
Chen, Muh-Shy
Ho, Tzyy-Chang
Clinical Characteristics of Highly Myopic Patients With Asymmetric Myopic Atrophic Maculopathy–Analysis Using Multimodal Imaging
title Clinical Characteristics of Highly Myopic Patients With Asymmetric Myopic Atrophic Maculopathy–Analysis Using Multimodal Imaging
title_full Clinical Characteristics of Highly Myopic Patients With Asymmetric Myopic Atrophic Maculopathy–Analysis Using Multimodal Imaging
title_fullStr Clinical Characteristics of Highly Myopic Patients With Asymmetric Myopic Atrophic Maculopathy–Analysis Using Multimodal Imaging
title_full_unstemmed Clinical Characteristics of Highly Myopic Patients With Asymmetric Myopic Atrophic Maculopathy–Analysis Using Multimodal Imaging
title_short Clinical Characteristics of Highly Myopic Patients With Asymmetric Myopic Atrophic Maculopathy–Analysis Using Multimodal Imaging
title_sort clinical characteristics of highly myopic patients with asymmetric myopic atrophic maculopathy–analysis using multimodal imaging
topic Retina
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7980047/
https://www.ncbi.nlm.nih.gov/pubmed/33724293
http://dx.doi.org/10.1167/iovs.62.3.21
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