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A cohort study: The Association Between Autoimmune Disorders and Leptospirosis
There are limited studies on the association between systemic autoimmune rheumatic diseases (SARDs) and leptospirosis. Therefore, this study aims to identify the effects of leptospirosis on the risks of developing SARDs with a nationwide retrospective cohort study. Patients with leptospirosis who di...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039877/ https://www.ncbi.nlm.nih.gov/pubmed/32094396 http://dx.doi.org/10.1038/s41598-020-60267-0 |
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author | Teh, Soon-Hian You, Ren-In Yang, Yu-Cih Hsu, Chung Y. Pang, Cheng-Yoong |
author_facet | Teh, Soon-Hian You, Ren-In Yang, Yu-Cih Hsu, Chung Y. Pang, Cheng-Yoong |
author_sort | Teh, Soon-Hian |
collection | PubMed |
description | There are limited studies on the association between systemic autoimmune rheumatic diseases (SARDs) and leptospirosis. Therefore, this study aims to identify the effects of leptospirosis on the risks of developing SARDs with a nationwide retrospective cohort study. Patients with leptospirosis who did not have a diagnosis of SARDs before the index date were enrolled from the Taiwan National Health Insurance Research Database between 2000 and 2010, as the leptospirosis cohort. For each patient with leptospirosis, one control without a history of leptospirosis and SARDs was randomly selected (non-leptospirosis cohort). Cox proportional hazards regression models were used to analyze the risk of SARDs according to sex, age, and comorbidities. Among the 23 million people in the cohort, 3,393 patients with leptospirosis (68.91% men, mean age 52.65 years) and 33,930 controls were followed for 18,778 and 232,999 person-years, respectively. The incidence of SARDs was higher in the leptospirosis cohort than in the non-leptospirosis cohort (1.38 vs 0.33 per 1000 person-years), with a hazard ratio (HR) of 4.42 (95% confidence interval [CI] = 2.82–6.92). The risk of developing SARDs was highest for leptospirosis patients aged ≥65 years (HR = 2.81% CI = 1.07–7.36) compared with patients aged ≤39 years. Patients with leptospirosis have a 4.42-fold higher risk of SARDs than that in the general population. Further research is warranted to investigate the mechanism underlying this association. |
format | Online Article Text |
id | pubmed-7039877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70398772020-02-28 A cohort study: The Association Between Autoimmune Disorders and Leptospirosis Teh, Soon-Hian You, Ren-In Yang, Yu-Cih Hsu, Chung Y. Pang, Cheng-Yoong Sci Rep Article There are limited studies on the association between systemic autoimmune rheumatic diseases (SARDs) and leptospirosis. Therefore, this study aims to identify the effects of leptospirosis on the risks of developing SARDs with a nationwide retrospective cohort study. Patients with leptospirosis who did not have a diagnosis of SARDs before the index date were enrolled from the Taiwan National Health Insurance Research Database between 2000 and 2010, as the leptospirosis cohort. For each patient with leptospirosis, one control without a history of leptospirosis and SARDs was randomly selected (non-leptospirosis cohort). Cox proportional hazards regression models were used to analyze the risk of SARDs according to sex, age, and comorbidities. Among the 23 million people in the cohort, 3,393 patients with leptospirosis (68.91% men, mean age 52.65 years) and 33,930 controls were followed for 18,778 and 232,999 person-years, respectively. The incidence of SARDs was higher in the leptospirosis cohort than in the non-leptospirosis cohort (1.38 vs 0.33 per 1000 person-years), with a hazard ratio (HR) of 4.42 (95% confidence interval [CI] = 2.82–6.92). The risk of developing SARDs was highest for leptospirosis patients aged ≥65 years (HR = 2.81% CI = 1.07–7.36) compared with patients aged ≤39 years. Patients with leptospirosis have a 4.42-fold higher risk of SARDs than that in the general population. Further research is warranted to investigate the mechanism underlying this association. Nature Publishing Group UK 2020-02-24 /pmc/articles/PMC7039877/ /pubmed/32094396 http://dx.doi.org/10.1038/s41598-020-60267-0 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 Teh, Soon-Hian You, Ren-In Yang, Yu-Cih Hsu, Chung Y. Pang, Cheng-Yoong A cohort study: The Association Between Autoimmune Disorders and Leptospirosis |
title | A cohort study: The Association Between Autoimmune Disorders and Leptospirosis |
title_full | A cohort study: The Association Between Autoimmune Disorders and Leptospirosis |
title_fullStr | A cohort study: The Association Between Autoimmune Disorders and Leptospirosis |
title_full_unstemmed | A cohort study: The Association Between Autoimmune Disorders and Leptospirosis |
title_short | A cohort study: The Association Between Autoimmune Disorders and Leptospirosis |
title_sort | cohort study: the association between autoimmune disorders and leptospirosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7039877/ https://www.ncbi.nlm.nih.gov/pubmed/32094396 http://dx.doi.org/10.1038/s41598-020-60267-0 |
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