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Serum Autoantibodies in Patients with Dry and Wet Age-Related Macular Degeneration

Background: To assess the serum autoantibody profile in patients with dry and exudative age-related macular degeneration compared with healthy volunteers to detect potential biomarkers, e.g., markers for progression of the disease. Materials and Methods: IgG Immunoreactivities were compared in patie...

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Autores principales: Korb, Christina A., Beck, Sabine, Wolters, Dominik, Lorenz, Katrin, Pfeiffer, Norbert, Grus, Franz H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9960765/
https://www.ncbi.nlm.nih.gov/pubmed/36836125
http://dx.doi.org/10.3390/jcm12041590
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author Korb, Christina A.
Beck, Sabine
Wolters, Dominik
Lorenz, Katrin
Pfeiffer, Norbert
Grus, Franz H.
author_facet Korb, Christina A.
Beck, Sabine
Wolters, Dominik
Lorenz, Katrin
Pfeiffer, Norbert
Grus, Franz H.
author_sort Korb, Christina A.
collection PubMed
description Background: To assess the serum autoantibody profile in patients with dry and exudative age-related macular degeneration compared with healthy volunteers to detect potential biomarkers, e.g., markers for progression of the disease. Materials and Methods: IgG Immunoreactivities were compared in patients suffering from dry age-related macular degeneration (AMD) (n = 20), patients with treatment-naive exudative AMD (n = 29) and healthy volunteers (n = 21). Serum was analysed by customized antigen microarrays containing 61 antigens. The statistical analysis was performed by univariate and multivariate analysis of variance, predictive data-mining methods and artificial neuronal networks were used to detect specific autoantibody patterns. Results: The immunoreactivities of dry and wet AMD patients were significantly different from each other and from controls. One of the most prominently changed reactivity was against alpha-synuclein (p ≤ 0.0034), which is known from other neurodegenerative diseases. Furthermore, reactivities against glyceraldehyde-3-phosphat-dehydrogenase (p ≤ 0.031) and Annexin V (p ≤ 0.034), which performs a major role in apoptotic processes, were significantly changed. Some immunoreacitvities were antithetic regulated in wet and dry-AMD, such as Vesicle transport-related protein (VTI-B). Conclusions: Comparison of autoantibody profiles in patients with dry and wet AMD revealed significantly altered immunoreactivities against proteins particularly found in immunological diseases, further neurodegenerative, apoptotic and autoimmune markers could be observed. A validation study has to explore if these antibody pattern can help to understand the underlying differences in pathogenesis, evaluate their prognostic value and if those could be possibly useful as additional therapeutic targets.
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spelling pubmed-99607652023-02-26 Serum Autoantibodies in Patients with Dry and Wet Age-Related Macular Degeneration Korb, Christina A. Beck, Sabine Wolters, Dominik Lorenz, Katrin Pfeiffer, Norbert Grus, Franz H. J Clin Med Article Background: To assess the serum autoantibody profile in patients with dry and exudative age-related macular degeneration compared with healthy volunteers to detect potential biomarkers, e.g., markers for progression of the disease. Materials and Methods: IgG Immunoreactivities were compared in patients suffering from dry age-related macular degeneration (AMD) (n = 20), patients with treatment-naive exudative AMD (n = 29) and healthy volunteers (n = 21). Serum was analysed by customized antigen microarrays containing 61 antigens. The statistical analysis was performed by univariate and multivariate analysis of variance, predictive data-mining methods and artificial neuronal networks were used to detect specific autoantibody patterns. Results: The immunoreactivities of dry and wet AMD patients were significantly different from each other and from controls. One of the most prominently changed reactivity was against alpha-synuclein (p ≤ 0.0034), which is known from other neurodegenerative diseases. Furthermore, reactivities against glyceraldehyde-3-phosphat-dehydrogenase (p ≤ 0.031) and Annexin V (p ≤ 0.034), which performs a major role in apoptotic processes, were significantly changed. Some immunoreacitvities were antithetic regulated in wet and dry-AMD, such as Vesicle transport-related protein (VTI-B). Conclusions: Comparison of autoantibody profiles in patients with dry and wet AMD revealed significantly altered immunoreactivities against proteins particularly found in immunological diseases, further neurodegenerative, apoptotic and autoimmune markers could be observed. A validation study has to explore if these antibody pattern can help to understand the underlying differences in pathogenesis, evaluate their prognostic value and if those could be possibly useful as additional therapeutic targets. MDPI 2023-02-17 /pmc/articles/PMC9960765/ /pubmed/36836125 http://dx.doi.org/10.3390/jcm12041590 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Korb, Christina A.
Beck, Sabine
Wolters, Dominik
Lorenz, Katrin
Pfeiffer, Norbert
Grus, Franz H.
Serum Autoantibodies in Patients with Dry and Wet Age-Related Macular Degeneration
title Serum Autoantibodies in Patients with Dry and Wet Age-Related Macular Degeneration
title_full Serum Autoantibodies in Patients with Dry and Wet Age-Related Macular Degeneration
title_fullStr Serum Autoantibodies in Patients with Dry and Wet Age-Related Macular Degeneration
title_full_unstemmed Serum Autoantibodies in Patients with Dry and Wet Age-Related Macular Degeneration
title_short Serum Autoantibodies in Patients with Dry and Wet Age-Related Macular Degeneration
title_sort serum autoantibodies in patients with dry and wet age-related macular degeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9960765/
https://www.ncbi.nlm.nih.gov/pubmed/36836125
http://dx.doi.org/10.3390/jcm12041590
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