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Angiotensin-Converting Enzyme Inhibitors and Active Tuberculosis: A Population-Based Study
Numerous epidemiological data suggest that the use of angiotensin-converting enzyme inhibitors (ACEis) can improve the clinical outcomes of pneumonia. Tuberculosis (TB) is an airborne bacteria like pneumonia, and we aimed to find out whether the use of ACEis can decrease the risk of active TB. We co...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902497/ https://www.ncbi.nlm.nih.gov/pubmed/27175655 http://dx.doi.org/10.1097/MD.0000000000003579 |
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author | Wu, Jiunn-Yih Lee, Meng-Tse Gabriel Lee, Si-Huei Lee, Shih-Hao Tsai, Yi-Wen Hsu, Shou-Chien Chang, Shy-Shin Lee, Chien-Chang |
author_facet | Wu, Jiunn-Yih Lee, Meng-Tse Gabriel Lee, Si-Huei Lee, Shih-Hao Tsai, Yi-Wen Hsu, Shou-Chien Chang, Shy-Shin Lee, Chien-Chang |
author_sort | Wu, Jiunn-Yih |
collection | PubMed |
description | Numerous epidemiological data suggest that the use of angiotensin-converting enzyme inhibitors (ACEis) can improve the clinical outcomes of pneumonia. Tuberculosis (TB) is an airborne bacteria like pneumonia, and we aimed to find out whether the use of ACEis can decrease the risk of active TB. We conducted a nested case–control analysis by using a 1 million longitudinally followed cohort, from Taiwan national health insurance research database. The rate ratios (RRs) for TB were estimated by conditional logistic regression, and adjusted using a TB-specific disease risk score (DRS) with 71 TB-related covariates. From January, 1997 to December, 2011, a total of 75,536 users of ACEis, and 7720 cases of new active TB were identified. Current use (DRS adjusted RR, 0.87 [95% CI, 0.78–0.97]), but not recent and past use of ACEis, was associated with a decrease in risk of active TB. Interestingly, it was found that chronic use (>90 days) of ACEis was associated with a further decrease in the risk of TB (aRR, 0.74, [95% CI, 0.66–0.83]). There was also a duration response effect, correlating decrease in TB risk with longer duration of ACEis use. The decrease in TB risk was also consistent across all patient subgroups (age, sex, heart failure, cerebrovascular diseases, myocardial infraction, renal diseases, and diabetes) and patients receiving other cardiovascular medicine. In this large population-based study, we found that subjects with recent and chronic use of ACEis were associated with decrease in TB risk. |
format | Online Article Text |
id | pubmed-4902497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-49024972016-06-27 Angiotensin-Converting Enzyme Inhibitors and Active Tuberculosis: A Population-Based Study Wu, Jiunn-Yih Lee, Meng-Tse Gabriel Lee, Si-Huei Lee, Shih-Hao Tsai, Yi-Wen Hsu, Shou-Chien Chang, Shy-Shin Lee, Chien-Chang Medicine (Baltimore) 4900 Numerous epidemiological data suggest that the use of angiotensin-converting enzyme inhibitors (ACEis) can improve the clinical outcomes of pneumonia. Tuberculosis (TB) is an airborne bacteria like pneumonia, and we aimed to find out whether the use of ACEis can decrease the risk of active TB. We conducted a nested case–control analysis by using a 1 million longitudinally followed cohort, from Taiwan national health insurance research database. The rate ratios (RRs) for TB were estimated by conditional logistic regression, and adjusted using a TB-specific disease risk score (DRS) with 71 TB-related covariates. From January, 1997 to December, 2011, a total of 75,536 users of ACEis, and 7720 cases of new active TB were identified. Current use (DRS adjusted RR, 0.87 [95% CI, 0.78–0.97]), but not recent and past use of ACEis, was associated with a decrease in risk of active TB. Interestingly, it was found that chronic use (>90 days) of ACEis was associated with a further decrease in the risk of TB (aRR, 0.74, [95% CI, 0.66–0.83]). There was also a duration response effect, correlating decrease in TB risk with longer duration of ACEis use. The decrease in TB risk was also consistent across all patient subgroups (age, sex, heart failure, cerebrovascular diseases, myocardial infraction, renal diseases, and diabetes) and patients receiving other cardiovascular medicine. In this large population-based study, we found that subjects with recent and chronic use of ACEis were associated with decrease in TB risk. Wolters Kluwer Health 2016-05-13 /pmc/articles/PMC4902497/ /pubmed/27175655 http://dx.doi.org/10.1097/MD.0000000000003579 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. http://creativecommons.org/licenses/by-nc-sa/4.0 |
spellingShingle | 4900 Wu, Jiunn-Yih Lee, Meng-Tse Gabriel Lee, Si-Huei Lee, Shih-Hao Tsai, Yi-Wen Hsu, Shou-Chien Chang, Shy-Shin Lee, Chien-Chang Angiotensin-Converting Enzyme Inhibitors and Active Tuberculosis: A Population-Based Study |
title | Angiotensin-Converting Enzyme Inhibitors and Active Tuberculosis: A Population-Based Study |
title_full | Angiotensin-Converting Enzyme Inhibitors and Active Tuberculosis: A Population-Based Study |
title_fullStr | Angiotensin-Converting Enzyme Inhibitors and Active Tuberculosis: A Population-Based Study |
title_full_unstemmed | Angiotensin-Converting Enzyme Inhibitors and Active Tuberculosis: A Population-Based Study |
title_short | Angiotensin-Converting Enzyme Inhibitors and Active Tuberculosis: A Population-Based Study |
title_sort | angiotensin-converting enzyme inhibitors and active tuberculosis: a population-based study |
topic | 4900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4902497/ https://www.ncbi.nlm.nih.gov/pubmed/27175655 http://dx.doi.org/10.1097/MD.0000000000003579 |
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