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Increased Cumulative Incidence of Dermatomyositis in Ulcerative Colitis: a Nationwide Cohort Study

On a molecular level, two autoimmune diseases: ulcerative colitis (UC) and dermatomyositis share common genetic determinants. On a clinical level, case reports evidenced the co-occurrence of these two diseases. We therefore hypothesize that UC is potentially associated with increased cumulative inci...

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Autores principales: Tseng, Chia-Chun, Chang, Shun-Jen, Liao, Wei-Ting, Chan, Ya-Ting, Tsai, Wen-Chan, Ou, Tsan-Teng, Wu, Cheng-Chin, Sung, Wan-Yu, Hsieh, Ming-Chia, Yen, Jeng-Hsien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914943/
https://www.ncbi.nlm.nih.gov/pubmed/27325143
http://dx.doi.org/10.1038/srep28175
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author Tseng, Chia-Chun
Chang, Shun-Jen
Liao, Wei-Ting
Chan, Ya-Ting
Tsai, Wen-Chan
Ou, Tsan-Teng
Wu, Cheng-Chin
Sung, Wan-Yu
Hsieh, Ming-Chia
Yen, Jeng-Hsien
author_facet Tseng, Chia-Chun
Chang, Shun-Jen
Liao, Wei-Ting
Chan, Ya-Ting
Tsai, Wen-Chan
Ou, Tsan-Teng
Wu, Cheng-Chin
Sung, Wan-Yu
Hsieh, Ming-Chia
Yen, Jeng-Hsien
author_sort Tseng, Chia-Chun
collection PubMed
description On a molecular level, two autoimmune diseases: ulcerative colitis (UC) and dermatomyositis share common genetic determinants. On a clinical level, case reports evidenced the co-occurrence of these two diseases. We therefore hypothesize that UC is potentially associated with increased cumulative incidence of dermatomyositis. The goals of this retrospective cohort study were to evaluate whether UC is associated with increased cumulative incidence of dermatomyositis independent of sex and age. For comparison, we also assessed the cumulative incidence of polymyositis in UC and control subjects. The study enrolled 3,133 UC subjects and 14,726 control subjects. The cumulative incidence of dermatomyositis was significantly higher in UC than that of control subjects (p = 0.026), but the cumulative incidence of polymyositis was comparable between UC and control subjects (p = 0.596). UC was independently associated with the increased incident dermatomyositis (hazard ratio: 6.19, 95% confidence interval = 1.77–21.59, p = 0.004) after adjusting for sex, age, and concomitant rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. Similar trends of increased dermatomyositis in UC were observed when patients were stratified based on sex and age. In conclusion, our findings suggest that UC is probably associated with increased cumulative incidence of dermatomyositis, independent of sex, age, and concomitant autoimmune diseases.
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spelling pubmed-49149432016-06-27 Increased Cumulative Incidence of Dermatomyositis in Ulcerative Colitis: a Nationwide Cohort Study Tseng, Chia-Chun Chang, Shun-Jen Liao, Wei-Ting Chan, Ya-Ting Tsai, Wen-Chan Ou, Tsan-Teng Wu, Cheng-Chin Sung, Wan-Yu Hsieh, Ming-Chia Yen, Jeng-Hsien Sci Rep Article On a molecular level, two autoimmune diseases: ulcerative colitis (UC) and dermatomyositis share common genetic determinants. On a clinical level, case reports evidenced the co-occurrence of these two diseases. We therefore hypothesize that UC is potentially associated with increased cumulative incidence of dermatomyositis. The goals of this retrospective cohort study were to evaluate whether UC is associated with increased cumulative incidence of dermatomyositis independent of sex and age. For comparison, we also assessed the cumulative incidence of polymyositis in UC and control subjects. The study enrolled 3,133 UC subjects and 14,726 control subjects. The cumulative incidence of dermatomyositis was significantly higher in UC than that of control subjects (p = 0.026), but the cumulative incidence of polymyositis was comparable between UC and control subjects (p = 0.596). UC was independently associated with the increased incident dermatomyositis (hazard ratio: 6.19, 95% confidence interval = 1.77–21.59, p = 0.004) after adjusting for sex, age, and concomitant rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. Similar trends of increased dermatomyositis in UC were observed when patients were stratified based on sex and age. In conclusion, our findings suggest that UC is probably associated with increased cumulative incidence of dermatomyositis, independent of sex, age, and concomitant autoimmune diseases. Nature Publishing Group 2016-06-21 /pmc/articles/PMC4914943/ /pubmed/27325143 http://dx.doi.org/10.1038/srep28175 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Tseng, Chia-Chun
Chang, Shun-Jen
Liao, Wei-Ting
Chan, Ya-Ting
Tsai, Wen-Chan
Ou, Tsan-Teng
Wu, Cheng-Chin
Sung, Wan-Yu
Hsieh, Ming-Chia
Yen, Jeng-Hsien
Increased Cumulative Incidence of Dermatomyositis in Ulcerative Colitis: a Nationwide Cohort Study
title Increased Cumulative Incidence of Dermatomyositis in Ulcerative Colitis: a Nationwide Cohort Study
title_full Increased Cumulative Incidence of Dermatomyositis in Ulcerative Colitis: a Nationwide Cohort Study
title_fullStr Increased Cumulative Incidence of Dermatomyositis in Ulcerative Colitis: a Nationwide Cohort Study
title_full_unstemmed Increased Cumulative Incidence of Dermatomyositis in Ulcerative Colitis: a Nationwide Cohort Study
title_short Increased Cumulative Incidence of Dermatomyositis in Ulcerative Colitis: a Nationwide Cohort Study
title_sort increased cumulative incidence of dermatomyositis in ulcerative colitis: a nationwide cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4914943/
https://www.ncbi.nlm.nih.gov/pubmed/27325143
http://dx.doi.org/10.1038/srep28175
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