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      Measuring the Contributions of Basal Laminar Deposit and Bruch's Membrane in Age-Related Macular Degeneration

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          Abstract

          Purpose

          Basal laminar deposit (BLamD) is a consistent finding in age-related macular degeneration (AMD). We quantified BLamD thickness, appearance, and topography in eyes of aged donors with and without AMD and evaluated its relationship to other components of the retinal pigment epithelium-basal lamina/Bruch's membrane (RPE-BL-BrM) complex.

          Methods

          Donor eyes ( n = 132) were classified as normal ( n = 54), early to intermediate AMD ( n = 24), geographic atrophy (GA; n = 13), and neovascular AMD (NV; n = 41). In high-resolution histology, we assessed RPE, BLamD, and BrM thicknesses and phenotypes at 3309 predefined locations in the central (foveal and perifovea) and superior (perifoveal) sections. Pre-mortem optical coherence tomography (OCT) imaging of a 90-year-old woman was compared to postmortem histopathology.

          Results

          In non-atrophic areas of AMD eyes, the RPE-BLamD is thick (normal = 13.7 µm, early-intermediate = 16.8 µm, GA = 17.4 µm, NV = 18.7 µm), because the BLamD is thick (normal = 0.3 µm, early-intermediate = 5.5 µm, GA = 4.1 µm, NV = 5.3 µm). RPE layer thickness is similar across these stages. Disease-associated variants of BLamD (thick, late, basal mounds) cluster subfoveally. A thick BLamD is visible on OCT as a hyporeflective split in the RPE-BL-BrM complex. BrM is thin (3.5 µm) in NV (normal = 4.2 µm, early to intermediate = 4.4 µm, and GA = 4.2 µm).

          Conclusions

          The RPE-BL-BrM complex is thick in AMD, driven by the accumulation and expansion of BLamD rather than expansion of either three-layer BrM, RPE-BL, or RPE. BLamD is clinically appreciable by OCT in some patients as a non-neovascular “split RPE-BL-BrM complex” or “double-layer sign.” BLamD may contribute toward the formation and progression of high-risk drusen yet also exhibit protective properties.

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          Most cited references106

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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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            Global causes of blindness and distance vision impairment 1990-2020: a systematic review and meta-analysis.

            Contemporary data for causes of vision impairment and blindness form an important basis of recommendations in public health policies. Refreshment of the Global Vision Database with recently published data sources permitted modelling of cause of vision loss data from 1990 to 2015, further disaggregation by cause, and forecasts to 2020.
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              A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

              Advanced age-related macular degeneration (AMD) is the leading cause of blindness in the elderly with limited therapeutic options. Here, we report on a study of >12 million variants including 163,714 directly genotyped, most rare, protein-altering variant. Analyzing 16,144 patients and 17,832 controls, we identify 52 independently associated common and rare variants (P < 5×10–8) distributed across 34 loci. While wet and dry AMD subtypes exhibit predominantly shared genetics, we identify the first signal specific to wet AMD, near MMP9 (difference-P = 4.1×10–10). Very rare coding variants (frequency < 0.1%) in CFH, CFI, and TIMP3 suggest causal roles for these genes, as does a splice variant in SLC16A8. Our results support the hypothesis that rare coding variants can pinpoint causal genes within known genetic loci and illustrate that applying the approach systematically to detect new loci requires extremely large sample sizes.
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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
                13 November 2020
                November 2020
                : 61
                : 13
                : 19
                Affiliations
                [1 ]Department of Ophthalmology and Visual Sciences, University of Alabama at Birmingham School of Medicine, Birmingham, Alabama, United States
                [2 ]The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Ophthalmology, and Chongqing Eye Institute, Chongqing, China
                [3 ]Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama, United States
                [4 ]Vitreous Retina Macula Consultants of New York, New York, New York, United States
                [5 ]Department of Ophthalmology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan
                [6 ]LuEsther T. Mertz Retinal Research Center, Manhattan Eye Ear and Throat Hospital, New York, New York, United States
                [7 ]Department of Ophthalmology, NYU Langone School of Medicine, New York, New York, United States
                [8 ]Columbia University College of Physicians and Surgeons, Harkness Eye Institute, New York, New York, United States
                Author notes
                Correspondence: Christine A. Curcio, Department of Ophthalmology and Visual Sciences, EyeSight Foundation of Alabama Vision Research Laboratories, 1670 University Boulevard, Room 360, University of Alabama at Birmingham School of Medicine, Birmingham, AL 35294-0019, USA; christinecurcio@ 123456uabmc.edu .

                AAS and LC are co-authors who contributed equally to this work.

                Article
                IOVS-20-31008
                10.1167/iovs.61.13.19
                7671869
                33186466
                d14afeb7-5baa-4187-9629-ec9200295b34
                Copyright 2020 The Authors

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

                History
                : 12 October 2020
                : 25 July 2020
                Page count
                Pages: 16
                Categories
                Retina
                Retina

                basal laminar deposit,basal laminar deposit (blamd),age-related macular degeneration (amd),age-related macular degeneration,histopathology,histology,retinal pigment epithelium,bruch's membrane,basal linear deposit,drusen,optical coherence tomography (oct),segmentation,neovascularization

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