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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Autores principales: Michelle Prasuhn, Caroline Hillers, Felix Rommel, Gabriela Riemekasten, Harald Heidecke, Khaled Nassar, Mahdy Ranjbar, Salvatore Grisanti, Aysegül Tura
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Publicado: MDPI AG 2021
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Acceso en línea:https://doaj.org/article/b0555f88cd534b928e5f44589455b39c
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spelling 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)
institution DOAJ
collection DOAJ
language EN
topic autoantibodies
age-related macular degeneration
biomarkers
AT1-receptor
PAR1
VEGF-A
Medicine
R
spellingShingle 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
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