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Association between inflammatory bowel disease and bullous pemphigoid: a population-based case–control study

The coexistence of inflammatory bowel disease (IBD) and bullous pemphigoid (BP) has been reported. No large-scale study to date has explored the relationship between these diseases. This population-based case-control study examined the association between IBD and BP by using a nationwide database. A...

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Autores principales: Chen, Yi-Ju, Juan, Chao-Kuei, Chang, Yun-Ting, Wu, Chun-Ying, Ho, Hsiu J., Tseng, Hsiao-Ching
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391771/
https://www.ncbi.nlm.nih.gov/pubmed/32728039
http://dx.doi.org/10.1038/s41598-020-69475-0
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author Chen, Yi-Ju
Juan, Chao-Kuei
Chang, Yun-Ting
Wu, Chun-Ying
Ho, Hsiu J.
Tseng, Hsiao-Ching
author_facet Chen, Yi-Ju
Juan, Chao-Kuei
Chang, Yun-Ting
Wu, Chun-Ying
Ho, Hsiu J.
Tseng, Hsiao-Ching
author_sort Chen, Yi-Ju
collection PubMed
description The coexistence of inflammatory bowel disease (IBD) and bullous pemphigoid (BP) has been reported. No large-scale study to date has explored the relationship between these diseases. This population-based case-control study examined the association between IBD and BP by using a nationwide database. A total of 5,263 BP patients and 21,052 age- and gender-, hospital visit number-matched controls were identified in the National Health Insurance Research Database of Taiwan (1997–2013). Demographic characteristics and comorbidities including IBD were compared. Logistic regression was conducted to examine the predicting factors for BP. The mean age at diagnosis was 74.88 years and 54.3% of subjects were male. BP patients tended to have more cardiovascular risk factors, autoimmune and neurologic comorbidities, and hematologic cancers than matched controls. There were 20 cases of IBD (0.38%), mostly ulcerative colitis (N = 17, 0.32%) among BP patients, compared to 33 IBD cases (0.16%) among controls (p < 0.001). Ulcerative colitis was found to be significantly associated with BP [adjusted odds ratio (OR) 3.60, 95% confidence interval (CI) 1.91–6.77, p < 0.001] on multivariate analysis. Treatment for IBD was not associated with BP development. Information about diet, lifestyle, alcohol consumption, and smoking habit was not available. We concluded that UC is independently associated with BP.
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spelling pubmed-73917712020-07-31 Association between inflammatory bowel disease and bullous pemphigoid: a population-based case–control study Chen, Yi-Ju Juan, Chao-Kuei Chang, Yun-Ting Wu, Chun-Ying Ho, Hsiu J. Tseng, Hsiao-Ching Sci Rep Article The coexistence of inflammatory bowel disease (IBD) and bullous pemphigoid (BP) has been reported. No large-scale study to date has explored the relationship between these diseases. This population-based case-control study examined the association between IBD and BP by using a nationwide database. A total of 5,263 BP patients and 21,052 age- and gender-, hospital visit number-matched controls were identified in the National Health Insurance Research Database of Taiwan (1997–2013). Demographic characteristics and comorbidities including IBD were compared. Logistic regression was conducted to examine the predicting factors for BP. The mean age at diagnosis was 74.88 years and 54.3% of subjects were male. BP patients tended to have more cardiovascular risk factors, autoimmune and neurologic comorbidities, and hematologic cancers than matched controls. There were 20 cases of IBD (0.38%), mostly ulcerative colitis (N = 17, 0.32%) among BP patients, compared to 33 IBD cases (0.16%) among controls (p < 0.001). Ulcerative colitis was found to be significantly associated with BP [adjusted odds ratio (OR) 3.60, 95% confidence interval (CI) 1.91–6.77, p < 0.001] on multivariate analysis. Treatment for IBD was not associated with BP development. Information about diet, lifestyle, alcohol consumption, and smoking habit was not available. We concluded that UC is independently associated with BP. Nature Publishing Group UK 2020-07-29 /pmc/articles/PMC7391771/ /pubmed/32728039 http://dx.doi.org/10.1038/s41598-020-69475-0 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
Chen, Yi-Ju
Juan, Chao-Kuei
Chang, Yun-Ting
Wu, Chun-Ying
Ho, Hsiu J.
Tseng, Hsiao-Ching
Association between inflammatory bowel disease and bullous pemphigoid: a population-based case–control study
title Association between inflammatory bowel disease and bullous pemphigoid: a population-based case–control study
title_full Association between inflammatory bowel disease and bullous pemphigoid: a population-based case–control study
title_fullStr Association between inflammatory bowel disease and bullous pemphigoid: a population-based case–control study
title_full_unstemmed Association between inflammatory bowel disease and bullous pemphigoid: a population-based case–control study
title_short Association between inflammatory bowel disease and bullous pemphigoid: a population-based case–control study
title_sort association between inflammatory bowel disease and bullous pemphigoid: a population-based case–control study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7391771/
https://www.ncbi.nlm.nih.gov/pubmed/32728039
http://dx.doi.org/10.1038/s41598-020-69475-0
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