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

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          Abstract

          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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          Most cited references47

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          Fiji: an open-source platform for biological-image analysis.

          Fiji is a distribution of the popular open-source software ImageJ focused on biological-image analysis. Fiji uses modern software engineering practices to combine powerful software libraries with a broad range of scripting languages to enable rapid prototyping of image-processing algorithms. Fiji facilitates the transformation of new algorithms into ImageJ plugins that can be shared with end users through an integrated update system. We propose Fiji as a platform for productive collaboration between computer science and biology research communities.
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            Myopic maculopathy: Current status and proposal for a new classification and grading system (ATN)

            Myopia is a highly frequent ocular disorder worldwide and pathologic myopia is the 4th most common cause of irreversible blindness in developed countries. Pathologic myopia is especially common in East Asian countries. Ocular alterations associated with pathologic myopia, especially those involving the macular area-defined as myopic maculopathy-are the leading causes of vision loss in patients with pathologic myopia. High myopia is defined as the presence of a highly negative refractive error (>-6 to -8 diopters) in the context of eye elongation (26-26.5 mm). Although the terms high myopia and pathologic myopia are often used interchangeably, they do not refer to the same eye disease. The two key factors driving the development of pathologic myopia are: 1) elongation of the axial length and 2) posterior staphyloma. The presence of posterior staphyloma, which is the most common finding in patients with pathologic myopia, is the key differentiating factor between high and pathologic myopia. The occurrence of staphyloma will, in most cases, eventually lead to other conditions such as atrophic, traction, or neovascular maculopathy. Posterior staphyloma is for instance, responsible for the differences between a myopic macular hole (MH)-with and without retinal detachment-and idiopathic MH. Posterior staphyloma typically induces retinal layer splitting, leading to foveoschisis in myopic MH, an important differentiating factor between myopic and emmetropic MH. Myopic maculopathy is a highly complex disease and current classification systems do not fully account for the numerous changes that occur in the macula of these patients. Therefore, a more comprehensive classification system is needed, for several important reasons. First, to more precisely define the disease stage to improve follow-up by enabling clinicians to more accurately monitor changes over time, which is essential given the progressive nature of this condition. Second, unification of the currently-available classification systems would establish standardized classification criteria that could be used to compare the findings from international multicentric studies. Finally, a more comprehensive classification system could help to improve our understanding of the genetic origins of this disease, which is clearly relevant given the interchangeable-but erroneous-use of the terms high and pathologic myopia in genetic research.
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              Quantitative OCT Angiography of the Retinal Microvasculature and the Choriocapillaris in Myopic Eyes.

              To study the retinal capillary microvasculature and the choriocapillaris (CC) in myopic eyes using quantitative optical coherence tomography angiography (OCTA) analysis.
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                Author and article information

                Journal
                Invest Ophthalmol Vis Sci
                Invest Ophthalmol Vis Sci
                iovs
                IOVS
                Investigative Ophthalmology & Visual Science
                The Association for Research in Vision and Ophthalmology
                0146-0404
                1552-5783
                16 March 2021
                March 2021
                : 62
                : 3
                : 21
                Affiliations
                [1 ]Department of Ophthalmology, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, Taiwan
                [2 ]Jin-Shan Branch, National Taiwan University Hospital, New Taipei City, Taiwan
                [3 ]Department of Ophthalmology, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan
                [4 ]Department of Ophthalmology, Fu Jen Catholic University Hospital, New Taipei City, Taiwan
                [5 ]Universal Eye Clinics, Taipei City, Taiwan
                [6 ]Department of Ophthalmology, Cardinal Tien Hospital, New Taipei City, Taiwan
                Author notes
                [* ]Correspondence: Tzyy-Chang Ho, Department of Ophthalmology, National Taiwan University Hospital, College of Medicine, National Taiwan University, No. 7, Chung-shan South Road, Taipei 10002, Taiwan; hotchang@ 123456ntu.edu.tw.
                Article
                IOVS-20-32018
                10.1167/iovs.62.3.21
                7980047
                33724293
                a0304300-ee78-43bc-a23b-c25b1455045c
                Copyright 2021 The Authors

                This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

                History
                : 19 February 2021
                : 17 December 2020
                Page count
                Pages: 7
                Categories
                Retina
                Retina

                asymmetric myopic atrophic maculopathy,high myopia,pathologic myopia,optical coherence tomography angiography,corvis st

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