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Evaluation of autoantibodies to desmoglein-2 in dogs with and without cardiac disease

Autoantibodies to desmoglein-2 have been associated with arrhythmogenic right ventricular cardiomyopathy (ARVC) in people. ARVC is a common disease in the Boxer dog. The role of anti-desmoglein-2 antibodies in Boxers with ARVC and correlation with disease status or severity is unknown. This prospect...

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Autores principales: Walker, Ashley L., Li, Ronald H. L., Nguyen, Nghi, Jauregui, Carina E., Meurs, Kathryn M., Gagnon, Allison L., Stern, Joshua A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043840/
https://www.ncbi.nlm.nih.gov/pubmed/36977772
http://dx.doi.org/10.1038/s41598-023-32081-x
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author Walker, Ashley L.
Li, Ronald H. L.
Nguyen, Nghi
Jauregui, Carina E.
Meurs, Kathryn M.
Gagnon, Allison L.
Stern, Joshua A.
author_facet Walker, Ashley L.
Li, Ronald H. L.
Nguyen, Nghi
Jauregui, Carina E.
Meurs, Kathryn M.
Gagnon, Allison L.
Stern, Joshua A.
author_sort Walker, Ashley L.
collection PubMed
description Autoantibodies to desmoglein-2 have been associated with arrhythmogenic right ventricular cardiomyopathy (ARVC) in people. ARVC is a common disease in the Boxer dog. The role of anti-desmoglein-2 antibodies in Boxers with ARVC and correlation with disease status or severity is unknown. This prospective study is the first to evaluate dogs of various breeds and cardiac disease state for anti-desmoglein-2 antibodies. The sera of 46 dogs (10 ARVC Boxers, 9 healthy Boxers, 10 Doberman Pinschers with dilated cardiomyopathy, 10 dogs with myxomatous mitral valve disease, and 7 healthy non-Boxer dogs) were assessed for antibody presence and concentration via Western blotting and densitometry. Anti-desmoglein-2 antibodies were detected in all dogs. Autoantibody expression did not differ between study groups and there was no correlation with age or body weight. In dogs with cardiac disease, there was weak correlation with left ventricular dilation (r = 0.423, p = 0.020) but not left atrial size (r = 0.160, p = 0.407). In ARVC Boxers there was strong correlation with the complexity of ventricular arrhythmias (r = 0.841, p = 0.007) but not total number of ectopic beats (r = 0.383, p = 0.313). Anti-desmoglein-2 antibodies were not disease specific in the studied population of dogs. Correlation with some measures of disease severity requires further study with larger populations.
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spelling pubmed-100438402023-03-28 Evaluation of autoantibodies to desmoglein-2 in dogs with and without cardiac disease Walker, Ashley L. Li, Ronald H. L. Nguyen, Nghi Jauregui, Carina E. Meurs, Kathryn M. Gagnon, Allison L. Stern, Joshua A. Sci Rep Article Autoantibodies to desmoglein-2 have been associated with arrhythmogenic right ventricular cardiomyopathy (ARVC) in people. ARVC is a common disease in the Boxer dog. The role of anti-desmoglein-2 antibodies in Boxers with ARVC and correlation with disease status or severity is unknown. This prospective study is the first to evaluate dogs of various breeds and cardiac disease state for anti-desmoglein-2 antibodies. The sera of 46 dogs (10 ARVC Boxers, 9 healthy Boxers, 10 Doberman Pinschers with dilated cardiomyopathy, 10 dogs with myxomatous mitral valve disease, and 7 healthy non-Boxer dogs) were assessed for antibody presence and concentration via Western blotting and densitometry. Anti-desmoglein-2 antibodies were detected in all dogs. Autoantibody expression did not differ between study groups and there was no correlation with age or body weight. In dogs with cardiac disease, there was weak correlation with left ventricular dilation (r = 0.423, p = 0.020) but not left atrial size (r = 0.160, p = 0.407). In ARVC Boxers there was strong correlation with the complexity of ventricular arrhythmias (r = 0.841, p = 0.007) but not total number of ectopic beats (r = 0.383, p = 0.313). Anti-desmoglein-2 antibodies were not disease specific in the studied population of dogs. Correlation with some measures of disease severity requires further study with larger populations. Nature Publishing Group UK 2023-03-28 /pmc/articles/PMC10043840/ /pubmed/36977772 http://dx.doi.org/10.1038/s41598-023-32081-x 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 Article
Walker, Ashley L.
Li, Ronald H. L.
Nguyen, Nghi
Jauregui, Carina E.
Meurs, Kathryn M.
Gagnon, Allison L.
Stern, Joshua A.
Evaluation of autoantibodies to desmoglein-2 in dogs with and without cardiac disease
title Evaluation of autoantibodies to desmoglein-2 in dogs with and without cardiac disease
title_full Evaluation of autoantibodies to desmoglein-2 in dogs with and without cardiac disease
title_fullStr Evaluation of autoantibodies to desmoglein-2 in dogs with and without cardiac disease
title_full_unstemmed Evaluation of autoantibodies to desmoglein-2 in dogs with and without cardiac disease
title_short Evaluation of autoantibodies to desmoglein-2 in dogs with and without cardiac disease
title_sort evaluation of autoantibodies to desmoglein-2 in dogs with and without cardiac disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10043840/
https://www.ncbi.nlm.nih.gov/pubmed/36977772
http://dx.doi.org/10.1038/s41598-023-32081-x
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