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Evolution of macular atrophy in eyes with neovascular age-related macular degeneration compared to fellow non-neovascular eyes
PURPOSE: Τo evaluate the evolution of macular atrophy (MA) in patients with neovascular AMD (nAMD), compared with their fellow eyes exhibiting dry AMD (dAMD). METHODS: This retrospective study included 124 patients from three centers treated with anti-VEGF in their nAMD eye and having dAMD in the fe...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667153/ https://www.ncbi.nlm.nih.gov/pubmed/37566302 http://dx.doi.org/10.1007/s00417-023-06168-0 |
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author | Blazaki, Styliani Blavakis, Emmanouil Chlouverakis, Gregory Bontzos, Georgios Chatziralli, Irini Smoustopoulos, Georgios Dimitriou, Eleni Stavrakakis, Anastasios Kabanarou, Stamatina Xirou, Tina Vavvas, Demetrios G. Tsilimbaris, Miltiadis K. |
author_facet | Blazaki, Styliani Blavakis, Emmanouil Chlouverakis, Gregory Bontzos, Georgios Chatziralli, Irini Smoustopoulos, Georgios Dimitriou, Eleni Stavrakakis, Anastasios Kabanarou, Stamatina Xirou, Tina Vavvas, Demetrios G. Tsilimbaris, Miltiadis K. |
author_sort | Blazaki, Styliani |
collection | PubMed |
description | PURPOSE: Τo evaluate the evolution of macular atrophy (MA) in patients with neovascular AMD (nAMD), compared with their fellow eyes exhibiting dry AMD (dAMD). METHODS: This retrospective study included 124 patients from three centers treated with anti-VEGF in their nAMD eye and having dAMD in the fellow eye. Patients without MA at baseline were analyzed to study the time to first MA development. Synchronous and unsynchronous time course of MA was also studied. MA was evaluated using near-infrared images, while all available optical coherence tomography (OCT) images were used to confirm the criteria proposed by the Classification of Atrophy Meetings group for complete MA. RESULTS: MA first detection in nAMD eyes increased significantly from year 2 to 6 compared to dAMD eyes. Over the study’s follow-up, 45.1% of nAMD-E developed MA, compared to 16.5% of fellow eyes (p < 0.001). When MA in the two eyes was compared in a synchronous paired manner over 4 years, nAMD eyes had an average MA progression rate of 0.275 mm/year versus 0.110 mm/year in their fellow dAMD eyes. Multivariate ANOVA revealed significant time (p < 0.001), eye (p = 0.003), and time-eye interaction (p < 0.001) effects. However, when MA did develop in dAMD eyes and was compared in an asynchronous manner to MA of nAMD eyes, it was found to progress faster in dAMD eyes (dAMD: 0.295 mm/year vs. nAMD: 0.176 mm/year) with a significant time-eye interaction (p = 0.015). CONCLUSIONS: In this study, a significant difference in MA incidence and progression was documented in eyes with nAMD under treatment, compared to fellow eye exhibiting dAMD. Eyes with nAMD tended to develop more MA compared to fellow dAMD eyes. However, when atrophy did develop in the fellow dAMD eyes, it progressed faster over time compared to MA in nAMD eyes. |
format | Online Article Text |
id | pubmed-10667153 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-106671532023-08-11 Evolution of macular atrophy in eyes with neovascular age-related macular degeneration compared to fellow non-neovascular eyes Blazaki, Styliani Blavakis, Emmanouil Chlouverakis, Gregory Bontzos, Georgios Chatziralli, Irini Smoustopoulos, Georgios Dimitriou, Eleni Stavrakakis, Anastasios Kabanarou, Stamatina Xirou, Tina Vavvas, Demetrios G. Tsilimbaris, Miltiadis K. Graefes Arch Clin Exp Ophthalmol Retinal Disorders PURPOSE: Τo evaluate the evolution of macular atrophy (MA) in patients with neovascular AMD (nAMD), compared with their fellow eyes exhibiting dry AMD (dAMD). METHODS: This retrospective study included 124 patients from three centers treated with anti-VEGF in their nAMD eye and having dAMD in the fellow eye. Patients without MA at baseline were analyzed to study the time to first MA development. Synchronous and unsynchronous time course of MA was also studied. MA was evaluated using near-infrared images, while all available optical coherence tomography (OCT) images were used to confirm the criteria proposed by the Classification of Atrophy Meetings group for complete MA. RESULTS: MA first detection in nAMD eyes increased significantly from year 2 to 6 compared to dAMD eyes. Over the study’s follow-up, 45.1% of nAMD-E developed MA, compared to 16.5% of fellow eyes (p < 0.001). When MA in the two eyes was compared in a synchronous paired manner over 4 years, nAMD eyes had an average MA progression rate of 0.275 mm/year versus 0.110 mm/year in their fellow dAMD eyes. Multivariate ANOVA revealed significant time (p < 0.001), eye (p = 0.003), and time-eye interaction (p < 0.001) effects. However, when MA did develop in dAMD eyes and was compared in an asynchronous manner to MA of nAMD eyes, it was found to progress faster in dAMD eyes (dAMD: 0.295 mm/year vs. nAMD: 0.176 mm/year) with a significant time-eye interaction (p = 0.015). CONCLUSIONS: In this study, a significant difference in MA incidence and progression was documented in eyes with nAMD under treatment, compared to fellow eye exhibiting dAMD. Eyes with nAMD tended to develop more MA compared to fellow dAMD eyes. However, when atrophy did develop in the fellow dAMD eyes, it progressed faster over time compared to MA in nAMD eyes. Springer Berlin Heidelberg 2023-08-11 2023 /pmc/articles/PMC10667153/ /pubmed/37566302 http://dx.doi.org/10.1007/s00417-023-06168-0 Text en © The Author(s) 2023 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 | Retinal Disorders Blazaki, Styliani Blavakis, Emmanouil Chlouverakis, Gregory Bontzos, Georgios Chatziralli, Irini Smoustopoulos, Georgios Dimitriou, Eleni Stavrakakis, Anastasios Kabanarou, Stamatina Xirou, Tina Vavvas, Demetrios G. Tsilimbaris, Miltiadis K. Evolution of macular atrophy in eyes with neovascular age-related macular degeneration compared to fellow non-neovascular eyes |
title | Evolution of macular atrophy in eyes with neovascular age-related macular degeneration compared to fellow non-neovascular eyes |
title_full | Evolution of macular atrophy in eyes with neovascular age-related macular degeneration compared to fellow non-neovascular eyes |
title_fullStr | Evolution of macular atrophy in eyes with neovascular age-related macular degeneration compared to fellow non-neovascular eyes |
title_full_unstemmed | Evolution of macular atrophy in eyes with neovascular age-related macular degeneration compared to fellow non-neovascular eyes |
title_short | Evolution of macular atrophy in eyes with neovascular age-related macular degeneration compared to fellow non-neovascular eyes |
title_sort | evolution of macular atrophy in eyes with neovascular age-related macular degeneration compared to fellow non-neovascular eyes |
topic | Retinal Disorders |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667153/ https://www.ncbi.nlm.nih.gov/pubmed/37566302 http://dx.doi.org/10.1007/s00417-023-06168-0 |
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