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Aqueous proteins help predict the response of patients with neovascular age-related macular degeneration to anti-VEGF therapy
BACKGROUND: To reduce the treatment burden for patients with neovascular age-related macular degeneration (nvAMD), emerging therapies targeting vascular endothelial growth factor (VEGF) are being designed to extend the interval between treatments, thereby minimizing the number of intraocular injecti...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Clinical Investigation
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759792/ https://www.ncbi.nlm.nih.gov/pubmed/34874918 http://dx.doi.org/10.1172/JCI144469 |
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author | Cao, Xuan Sanchez, Jaron Castillo Dinabandhu, Aumreetam Guo, Chuanyu Patel, Tapan P. Yang, Zhiyong Hu, Ming-Wen Chen, Lijun Wang, Yuefan Malik, Danyal Jee, Kathleen Daoud, Yassine J. Handa, James T. Zhang, Hui Qian, Jiang Montaner, Silvia Sodhi, Akrit |
author_facet | Cao, Xuan Sanchez, Jaron Castillo Dinabandhu, Aumreetam Guo, Chuanyu Patel, Tapan P. Yang, Zhiyong Hu, Ming-Wen Chen, Lijun Wang, Yuefan Malik, Danyal Jee, Kathleen Daoud, Yassine J. Handa, James T. Zhang, Hui Qian, Jiang Montaner, Silvia Sodhi, Akrit |
author_sort | Cao, Xuan |
collection | PubMed |
description | BACKGROUND: To reduce the treatment burden for patients with neovascular age-related macular degeneration (nvAMD), emerging therapies targeting vascular endothelial growth factor (VEGF) are being designed to extend the interval between treatments, thereby minimizing the number of intraocular injections. However, which patients will benefit from longer-acting agents is not clear. METHODS: Eyes with nvAMD (n = 122) underwent 3 consecutive monthly injections with currently available anti-VEGF therapies, followed by a treat-and-extend protocol. Patients who remained quiescent 12 weeks from their prior treatment entered a treatment pause and were switched to pro re nata (PRN) treatment (based on vision, clinical exam, and/or imaging studies). Proteomic analysis was performed on aqueous fluid to identify proteins that correlate with patients’ response to treatment. RESULTS: At the end of 1 year, 38 of 122 eyes (31%) entered a treatment pause (≥30 weeks). Conversely, 21 of 122 eyes (17%) failed extension and required monthly treatment at the end of year 1. Proteomic analysis of aqueous fluid identified proteins that correlated with patients’ response to treatment, including proteins previously implicated in AMD pathogenesis. Interestingly, apolipoprotein-B100 (ApoB100), a principal component of drusen implicated in the progression of nonneovascular AMD, was increased in treated patients who required less frequent injections. ApoB100 expression was higher in AMD eyes compared with controls but was lower in eyes that develop choroidal neovascularization (CNV), consistent with a protective role. Accordingly, mice overexpressing ApoB100 were partially protected from laser-induced CNV. FUNDING: This work was supported by the National Eye Institute, National Institutes of Health grants R01EY029750, R01EY025705, and R01 EY27961; the Research to Prevent Blindness, Inc.; the Alcon Research Institute; and Johns Hopkins University through the Robert Bond Welch and Branna and Irving Sisenwein professorships in ophthalmology. CONCLUSION: Aqueous biomarkers could help identify patients with nvAMD who may not require or benefit from long-term treatment with anti-VEGF therapy. |
format | Online Article Text |
id | pubmed-8759792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-87597922022-01-19 Aqueous proteins help predict the response of patients with neovascular age-related macular degeneration to anti-VEGF therapy Cao, Xuan Sanchez, Jaron Castillo Dinabandhu, Aumreetam Guo, Chuanyu Patel, Tapan P. Yang, Zhiyong Hu, Ming-Wen Chen, Lijun Wang, Yuefan Malik, Danyal Jee, Kathleen Daoud, Yassine J. Handa, James T. Zhang, Hui Qian, Jiang Montaner, Silvia Sodhi, Akrit J Clin Invest Clinical Medicine BACKGROUND: To reduce the treatment burden for patients with neovascular age-related macular degeneration (nvAMD), emerging therapies targeting vascular endothelial growth factor (VEGF) are being designed to extend the interval between treatments, thereby minimizing the number of intraocular injections. However, which patients will benefit from longer-acting agents is not clear. METHODS: Eyes with nvAMD (n = 122) underwent 3 consecutive monthly injections with currently available anti-VEGF therapies, followed by a treat-and-extend protocol. Patients who remained quiescent 12 weeks from their prior treatment entered a treatment pause and were switched to pro re nata (PRN) treatment (based on vision, clinical exam, and/or imaging studies). Proteomic analysis was performed on aqueous fluid to identify proteins that correlate with patients’ response to treatment. RESULTS: At the end of 1 year, 38 of 122 eyes (31%) entered a treatment pause (≥30 weeks). Conversely, 21 of 122 eyes (17%) failed extension and required monthly treatment at the end of year 1. Proteomic analysis of aqueous fluid identified proteins that correlated with patients’ response to treatment, including proteins previously implicated in AMD pathogenesis. Interestingly, apolipoprotein-B100 (ApoB100), a principal component of drusen implicated in the progression of nonneovascular AMD, was increased in treated patients who required less frequent injections. ApoB100 expression was higher in AMD eyes compared with controls but was lower in eyes that develop choroidal neovascularization (CNV), consistent with a protective role. Accordingly, mice overexpressing ApoB100 were partially protected from laser-induced CNV. FUNDING: This work was supported by the National Eye Institute, National Institutes of Health grants R01EY029750, R01EY025705, and R01 EY27961; the Research to Prevent Blindness, Inc.; the Alcon Research Institute; and Johns Hopkins University through the Robert Bond Welch and Branna and Irving Sisenwein professorships in ophthalmology. CONCLUSION: Aqueous biomarkers could help identify patients with nvAMD who may not require or benefit from long-term treatment with anti-VEGF therapy. American Society for Clinical Investigation 2022-01-18 2022-01-18 /pmc/articles/PMC8759792/ /pubmed/34874918 http://dx.doi.org/10.1172/JCI144469 Text en © 2022 Cao et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Clinical Medicine Cao, Xuan Sanchez, Jaron Castillo Dinabandhu, Aumreetam Guo, Chuanyu Patel, Tapan P. Yang, Zhiyong Hu, Ming-Wen Chen, Lijun Wang, Yuefan Malik, Danyal Jee, Kathleen Daoud, Yassine J. Handa, James T. Zhang, Hui Qian, Jiang Montaner, Silvia Sodhi, Akrit Aqueous proteins help predict the response of patients with neovascular age-related macular degeneration to anti-VEGF therapy |
title | Aqueous proteins help predict the response of patients with neovascular age-related macular degeneration to anti-VEGF therapy |
title_full | Aqueous proteins help predict the response of patients with neovascular age-related macular degeneration to anti-VEGF therapy |
title_fullStr | Aqueous proteins help predict the response of patients with neovascular age-related macular degeneration to anti-VEGF therapy |
title_full_unstemmed | Aqueous proteins help predict the response of patients with neovascular age-related macular degeneration to anti-VEGF therapy |
title_short | Aqueous proteins help predict the response of patients with neovascular age-related macular degeneration to anti-VEGF therapy |
title_sort | aqueous proteins help predict the response of patients with neovascular age-related macular degeneration to anti-vegf therapy |
topic | Clinical Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8759792/ https://www.ncbi.nlm.nih.gov/pubmed/34874918 http://dx.doi.org/10.1172/JCI144469 |
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