Specific Autoantibodies in Neovascular Age-Related Macular Degeneration: Evaluation of Morphological and Functional Progression over Five Years
(1) Background: Altered levels of autoantibodies (aab) and their networks have been identified as biomarkers for various diseases. Neovascular age-related macular degeneration (nAMD) is a leading cause for central vision loss worldwide with highly variable inter- and intraindividual disease courses....
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oai:doaj.org-article:b0555f88cd534b928e5f44589455b39c2021-11-25T18:08:01ZSpecific Autoantibodies in Neovascular Age-Related Macular Degeneration: Evaluation of Morphological and Functional Progression over Five Years10.3390/jpm111112072075-4426https://doaj.org/article/b0555f88cd534b928e5f44589455b39c2021-11-01T00:00:00Zhttps://www.mdpi.com/2075-4426/11/11/1207https://doaj.org/toc/2075-4426(1) Background: Altered levels of autoantibodies (aab) and their networks have been identified as biomarkers for various diseases. Neovascular age-related macular degeneration (nAMD) is a leading cause for central vision loss worldwide with highly variable inter- and intraindividual disease courses. Certain aab networks could help in daily routine to identify patients with a high disease activity who need to be visited and treated more regularly. (2) Methods: We analyzed levels of aab against Angiotensin II receptor type 1 (AT1-receptor), Protease-activated receptors (PAR1), vascular endothelial growth factor (VEGF) -A, VEGF-B, and VEGF-receptor 2 in sera of 164 nAMD patients. In a follow-up period of five years, we evaluated changes in functional and morphological characteristics. Using correlation analyses, multiple regression models, and receiver operator characteristics, we assessed whether the five aab have a clinical significance as biomarkers that correspond to the clinical properties. (3) Results: Neither the analyzed aab individually nor taken together as a network showed statistically significant results that would allow us to draw conclusions on the clinical five-year course in nAMD patients. (4) Conclusions: The five aab that we analyzed do not correspond to the clinical five-year course of nAMD patients. However, larger, prospective studies should reevaluate different and more aab to gain deeper insights.Michelle PrasuhnCaroline HillersFelix RommelGabriela RiemekastenHarald HeideckeKhaled NassarMahdy RanjbarSalvatore GrisantiAysegül TuraMDPI AGarticleautoantibodiesage-related macular degenerationbiomarkersAT1-receptorPAR1VEGF-AMedicineRENJournal of Personalized Medicine, Vol 11, Iss 1207, p 1207 (2021) |
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autoantibodies age-related macular degeneration biomarkers AT1-receptor PAR1 VEGF-A Medicine R |
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autoantibodies age-related macular degeneration biomarkers AT1-receptor PAR1 VEGF-A Medicine R Michelle Prasuhn Caroline Hillers Felix Rommel Gabriela Riemekasten Harald Heidecke Khaled Nassar Mahdy Ranjbar Salvatore Grisanti Aysegül Tura Specific Autoantibodies in Neovascular Age-Related Macular Degeneration: Evaluation of Morphological and Functional Progression over Five Years |
description |
(1) Background: Altered levels of autoantibodies (aab) and their networks have been identified as biomarkers for various diseases. Neovascular age-related macular degeneration (nAMD) is a leading cause for central vision loss worldwide with highly variable inter- and intraindividual disease courses. Certain aab networks could help in daily routine to identify patients with a high disease activity who need to be visited and treated more regularly. (2) Methods: We analyzed levels of aab against Angiotensin II receptor type 1 (AT1-receptor), Protease-activated receptors (PAR1), vascular endothelial growth factor (VEGF) -A, VEGF-B, and VEGF-receptor 2 in sera of 164 nAMD patients. In a follow-up period of five years, we evaluated changes in functional and morphological characteristics. Using correlation analyses, multiple regression models, and receiver operator characteristics, we assessed whether the five aab have a clinical significance as biomarkers that correspond to the clinical properties. (3) Results: Neither the analyzed aab individually nor taken together as a network showed statistically significant results that would allow us to draw conclusions on the clinical five-year course in nAMD patients. (4) Conclusions: The five aab that we analyzed do not correspond to the clinical five-year course of nAMD patients. However, larger, prospective studies should reevaluate different and more aab to gain deeper insights. |
format |
article |
author |
Michelle Prasuhn Caroline Hillers Felix Rommel Gabriela Riemekasten Harald Heidecke Khaled Nassar Mahdy Ranjbar Salvatore Grisanti Aysegül Tura |
author_facet |
Michelle Prasuhn Caroline Hillers Felix Rommel Gabriela Riemekasten Harald Heidecke Khaled Nassar Mahdy Ranjbar Salvatore Grisanti Aysegül Tura |
author_sort |
Michelle Prasuhn |
title |
Specific Autoantibodies in Neovascular Age-Related Macular Degeneration: Evaluation of Morphological and Functional Progression over Five Years |
title_short |
Specific Autoantibodies in Neovascular Age-Related Macular Degeneration: Evaluation of Morphological and Functional Progression over Five Years |
title_full |
Specific Autoantibodies in Neovascular Age-Related Macular Degeneration: Evaluation of Morphological and Functional Progression over Five Years |
title_fullStr |
Specific Autoantibodies in Neovascular Age-Related Macular Degeneration: Evaluation of Morphological and Functional Progression over Five Years |
title_full_unstemmed |
Specific Autoantibodies in Neovascular Age-Related Macular Degeneration: Evaluation of Morphological and Functional Progression over Five Years |
title_sort |
specific autoantibodies in neovascular age-related macular degeneration: evaluation of morphological and functional progression over five years |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/b0555f88cd534b928e5f44589455b39c |
work_keys_str_mv |
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