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The Correlation between New Serological Markers and Disease Phenotype and Activation in Inflammatory Bowel Disease

Background: The aim of the study is to assess the correlation between a new antibody panel that is developed against glycans on Crohn’s disease (CD) and ulcerative colitis (UC) differentiative diagnosis and disease properties. Methods: In the study, 137 CD and 122 UC patients and 90 controls were in...

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Autores principales: Yorulmaz, Elif, Adalı, Gupse, Yorulmaz, Hatice, Taşan, Güralp, Gürses, Seval, Ayaş, Mehmet Ramazan, Tuncer, İlyas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Association of Gastroerterology and Hepatology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489435/
https://www.ncbi.nlm.nih.gov/pubmed/36619271
http://dx.doi.org/10.34172/mejdd.2022.286
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author Yorulmaz, Elif
Adalı, Gupse
Yorulmaz, Hatice
Taşan, Güralp
Gürses, Seval
Ayaş, Mehmet Ramazan
Tuncer, İlyas
author_facet Yorulmaz, Elif
Adalı, Gupse
Yorulmaz, Hatice
Taşan, Güralp
Gürses, Seval
Ayaş, Mehmet Ramazan
Tuncer, İlyas
author_sort Yorulmaz, Elif
collection PubMed
description Background: The aim of the study is to assess the correlation between a new antibody panel that is developed against glycans on Crohn’s disease (CD) and ulcerative colitis (UC) differentiative diagnosis and disease properties. Methods: In the study, 137 CD and 122 UC patients and 90 controls were included. Anti-saccharomyces cerevisiae IgG (ASCA), anti-laminaribioside IgG (ALCA), anti-chitobioside IgA (ACCA), and anti-mannobioside IgG (AMCA) were tested in serum. Results: While at least 1 of the other 3 serological markers was positive in 89% of ASCA-positive patients, at least 1 of the other 3 serological markers was positive in 77% of ASCA-negative patients. Positivity ratio for a single anticarbohydrate was ALCA 18 (22%), ACCA 5 (12%), and AMCA 16 (23%). A significant correlation was found between ASCA positivity (P<0.001) in operated patients and between ASCA, ALCA, and ACCA positivity (P<0.05) in patients with stricturing and fistulizing CD. According to the ROC analysis, ASCA was found to have the highest area under the curve (0.70-0.82) (correlation coefficient interval 95%). A significant correlation was found between ASCA, ALCA, and ACCA positivity and high serum antibody levels and disease activation (P<0.05). Conclusion: ASCA, ALCA, and ACCA were found to be correlated with the disease complication and activation in CD. ASCA and ALCA were determined as the best markers in the differentiation between CD and UC.
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spelling pubmed-94894352023-01-06 The Correlation between New Serological Markers and Disease Phenotype and Activation in Inflammatory Bowel Disease Yorulmaz, Elif Adalı, Gupse Yorulmaz, Hatice Taşan, Güralp Gürses, Seval Ayaş, Mehmet Ramazan Tuncer, İlyas Middle East J Dig Dis Original Article Background: The aim of the study is to assess the correlation between a new antibody panel that is developed against glycans on Crohn’s disease (CD) and ulcerative colitis (UC) differentiative diagnosis and disease properties. Methods: In the study, 137 CD and 122 UC patients and 90 controls were included. Anti-saccharomyces cerevisiae IgG (ASCA), anti-laminaribioside IgG (ALCA), anti-chitobioside IgA (ACCA), and anti-mannobioside IgG (AMCA) were tested in serum. Results: While at least 1 of the other 3 serological markers was positive in 89% of ASCA-positive patients, at least 1 of the other 3 serological markers was positive in 77% of ASCA-negative patients. Positivity ratio for a single anticarbohydrate was ALCA 18 (22%), ACCA 5 (12%), and AMCA 16 (23%). A significant correlation was found between ASCA positivity (P<0.001) in operated patients and between ASCA, ALCA, and ACCA positivity (P<0.05) in patients with stricturing and fistulizing CD. According to the ROC analysis, ASCA was found to have the highest area under the curve (0.70-0.82) (correlation coefficient interval 95%). A significant correlation was found between ASCA, ALCA, and ACCA positivity and high serum antibody levels and disease activation (P<0.05). Conclusion: ASCA, ALCA, and ACCA were found to be correlated with the disease complication and activation in CD. ASCA and ALCA were determined as the best markers in the differentiation between CD and UC. Iranian Association of Gastroerterology and Hepatology 2022-07 2022-07-30 /pmc/articles/PMC9489435/ /pubmed/36619271 http://dx.doi.org/10.34172/mejdd.2022.286 Text en © 2022 Middle East Journal of Digestive Diseases https://creativecommons.org/licenses/by-nc/4.0/This work is published by Middle East Journal of Digestive Diseases as an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Article
Yorulmaz, Elif
Adalı, Gupse
Yorulmaz, Hatice
Taşan, Güralp
Gürses, Seval
Ayaş, Mehmet Ramazan
Tuncer, İlyas
The Correlation between New Serological Markers and Disease Phenotype and Activation in Inflammatory Bowel Disease
title The Correlation between New Serological Markers and Disease Phenotype and Activation in Inflammatory Bowel Disease
title_full The Correlation between New Serological Markers and Disease Phenotype and Activation in Inflammatory Bowel Disease
title_fullStr The Correlation between New Serological Markers and Disease Phenotype and Activation in Inflammatory Bowel Disease
title_full_unstemmed The Correlation between New Serological Markers and Disease Phenotype and Activation in Inflammatory Bowel Disease
title_short The Correlation between New Serological Markers and Disease Phenotype and Activation in Inflammatory Bowel Disease
title_sort correlation between new serological markers and disease phenotype and activation in inflammatory bowel disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9489435/
https://www.ncbi.nlm.nih.gov/pubmed/36619271
http://dx.doi.org/10.34172/mejdd.2022.286
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