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Impact of immune-mediated diseases in inflammatory bowel disease and implications in therapeutic approach
Inflammatory bowel diseases (IBD) belong to the group of immune-mediated diseases (IMIDs). The effect of associated IMIDs in the prognosis in IBD is nowadays unknown. To describe IMIDs associated to IBD patients and evaluate differences linked to the presence or absence of IMIDs. A unicentric retros...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330038/ https://www.ncbi.nlm.nih.gov/pubmed/32612137 http://dx.doi.org/10.1038/s41598-020-67710-2 |
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author | García, M. J. Pascual, M. Del Pozo, C. Díaz-González, A. Castro, B. Rasines, L. Crespo, J. Rivero, M. |
author_facet | García, M. J. Pascual, M. Del Pozo, C. Díaz-González, A. Castro, B. Rasines, L. Crespo, J. Rivero, M. |
author_sort | García, M. J. |
collection | PubMed |
description | Inflammatory bowel diseases (IBD) belong to the group of immune-mediated diseases (IMIDs). The effect of associated IMIDs in the prognosis in IBD is nowadays unknown. To describe IMIDs associated to IBD patients and evaluate differences linked to the presence or absence of IMIDs. A unicentric retrospective descriptive study was designed. A cohort of 1,448 patients were categorized according to the presence of IMIDs. Clinical characteristics were obtained from IBD database. Univariate and multivariate analysis were performed. 385 patients were diagnosed with associated IMIDs while 1,063 had no associated IMIDs. A prevalence of 26.6% IMIDs associated to IBD was observed. Asthma, skin psoriasis and rheumatoid diseases were most commonly found. Factors associated to the presence of IMIDs were women (OR 1.48; 95 CI 1.17–1.87) and Crohn’s disease (OR 1.35; 95 CI 1.07–1.70). Patients with associated IMIDs required more immunomodulator (OR 1.61; 95 CI 1.27–2.43) and biological treatment (OR 1.81; 95 CI 1.47–2.43). More surgical risk was observed in multivariate analysis in those patients diagnosed with IMIDs prior to the onset of IBD (OR 3.71; 95% CI 2.1–6.56). We considered the presence of IMIDs a poor prognostic factor and suggest a closer monitoring of these patients. |
format | Online Article Text |
id | pubmed-7330038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73300382020-07-06 Impact of immune-mediated diseases in inflammatory bowel disease and implications in therapeutic approach García, M. J. Pascual, M. Del Pozo, C. Díaz-González, A. Castro, B. Rasines, L. Crespo, J. Rivero, M. Sci Rep Article Inflammatory bowel diseases (IBD) belong to the group of immune-mediated diseases (IMIDs). The effect of associated IMIDs in the prognosis in IBD is nowadays unknown. To describe IMIDs associated to IBD patients and evaluate differences linked to the presence or absence of IMIDs. A unicentric retrospective descriptive study was designed. A cohort of 1,448 patients were categorized according to the presence of IMIDs. Clinical characteristics were obtained from IBD database. Univariate and multivariate analysis were performed. 385 patients were diagnosed with associated IMIDs while 1,063 had no associated IMIDs. A prevalence of 26.6% IMIDs associated to IBD was observed. Asthma, skin psoriasis and rheumatoid diseases were most commonly found. Factors associated to the presence of IMIDs were women (OR 1.48; 95 CI 1.17–1.87) and Crohn’s disease (OR 1.35; 95 CI 1.07–1.70). Patients with associated IMIDs required more immunomodulator (OR 1.61; 95 CI 1.27–2.43) and biological treatment (OR 1.81; 95 CI 1.47–2.43). More surgical risk was observed in multivariate analysis in those patients diagnosed with IMIDs prior to the onset of IBD (OR 3.71; 95% CI 2.1–6.56). We considered the presence of IMIDs a poor prognostic factor and suggest a closer monitoring of these patients. Nature Publishing Group UK 2020-07-01 /pmc/articles/PMC7330038/ /pubmed/32612137 http://dx.doi.org/10.1038/s41598-020-67710-2 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article García, M. J. Pascual, M. Del Pozo, C. Díaz-González, A. Castro, B. Rasines, L. Crespo, J. Rivero, M. Impact of immune-mediated diseases in inflammatory bowel disease and implications in therapeutic approach |
title | Impact of immune-mediated diseases in inflammatory bowel disease and implications in therapeutic approach |
title_full | Impact of immune-mediated diseases in inflammatory bowel disease and implications in therapeutic approach |
title_fullStr | Impact of immune-mediated diseases in inflammatory bowel disease and implications in therapeutic approach |
title_full_unstemmed | Impact of immune-mediated diseases in inflammatory bowel disease and implications in therapeutic approach |
title_short | Impact of immune-mediated diseases in inflammatory bowel disease and implications in therapeutic approach |
title_sort | impact of immune-mediated diseases in inflammatory bowel disease and implications in therapeutic approach |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330038/ https://www.ncbi.nlm.nih.gov/pubmed/32612137 http://dx.doi.org/10.1038/s41598-020-67710-2 |
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