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   <ref-type name="Journal Article">17</ref-type>
   <contributors>
    <authors>
     <author>Jonas, J.B.</author>
     <author>Jonas, R.A.</author>
     <author>Bikbov, M.M.</author>
     <author>Kazakbaeva, G.M.</author>
     <author>Wan, Ya.X.</author>
     <author>Nangia, V.</author>
     <author>Panda-Jonas, S.</author>
    </authors>
   </contributors>
   <titles>
    <title>Macular Atrophic versus Subretinal Proliferative Changes in Myopic and Age-Related Macular Degeneration</title>
   </titles>
   <keywords>
    <keyword>age-related macular degeneration</keyword>
    <keyword>macula atrophy</keyword>
    <keyword>pathologic myopia</keyword>
    <keyword>subretinal fibrosis</keyword>
    <keyword>subretinal proliferation</keyword>
    <keyword>Scopus</keyword>
    <keyword>Web of Science</keyword>
   </keywords>
   <dates>
    <year>2025</year>
    <pub-dates>
     <date>2026-05-23</date>
    </pub-dates>
   </dates>
   <doi>10.1016/j.xops.2025.100885</doi>
   <journal>OPHTHALMOLOGY SCIENCE</journal>
   <abstract>Objective: To assess the prevalences of subfoveal retinal pigment epithelium (RPE) loss versus subfoveal tissue&#13;
proliferation as causes of vision loss in patients with late-stage age-related macular degeneration (AMD) or myopic&#13;
macular atrophy.&#13;
Design: Population-based studies conducted in Russia, China, and India and histological examination of&#13;
enucleated human globes.&#13;
Participants: The Russian Ural Eye and Medical Study (n = 5899 participants; age: ≥40 years), Ural Very Old&#13;
Study (n = 1526; age: 85+ years), Beijing Eye Study (n = 3468; age: ≥40 years), and Central India Eye and Medical&#13;
Study (n = 4711) were conducted in rural and urban regions in Bashkortostan/Russia, Beijing/China, and Nagpur/India,&#13;
respectively. The histological study part included human eyes enucleated because of reasons like malignant melanomas, or were post mortem enucleated.&#13;
Methods: The participants underwent a series of general medical and ophthalmological examinations including&#13;
OCT of the macula. In the histological study part, the enucleated globes were histomorphometrically examined.&#13;
Main Outcome Measures: Presence of RPE loss and of subretinal proliferations.&#13;
Results: In all 4 population-based studies combined, late-stage AMD and myopic macular atrophy were detected&#13;
in 291 eyes and 46 eyes, respectively. Retinal pigment epithelium cell loss was dominant in 136 (94%) out of 145 eyes&#13;
with geographic atrophy and in 35 (76%) out of 46 eyes with myopic macular atrophy, whereas subretinal proliferations&#13;
were predominantly present in 127 (87%) out of 146 eyes with neovascular AMD. Among all 337 eyes with late AMD or&#13;
myopic macular atrophy, RPE loss was the main cause for vision loss in 190 (56%) eyes and subretinal proliferations in&#13;
147 (44%) eyes, with no significant difference (P &gt; 0.05) between the study cohorts. In the histological specimen,&#13;
subretinal proliferations included melanin-bearing cells in contact with a periodic acid—Schiff-positive membrane,&#13;
resembling RPE cells.&#13;
Conclusions: Subretinal proliferations in the foveal region were the main reason for central visual acuity loss in&#13;
44% of all eyes with late AMD or myopic macular atrophy in 4 population-based studies. Subretinal foveal RPE cell&#13;
proliferation and RPE loss are roughly equally important as a cause of vision loss in AMD and myopic macular atrophy.</abstract>
   <urls>
    <web-urls>
     <url>https://repo.bashgmu.ru/publication/5400</url>
    </web-urls>
    <pdf-urls>
     <url>https://repo.bashgmu.ru/files/5594</url>
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