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Latent Tuberculosis Infection and the Risk of Subsequent Cancer
The association of latent tuberculosis infection (LTBI) with subsequent cancer remains unclear. We investigated the risk of future cancer among tuberculosis (TB) contacts with or without subsequent TB activation. Using the Taiwan National Health Insurance Research Database, we conducted a nationwide...
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/PMC5291550/ https://www.ncbi.nlm.nih.gov/pubmed/26825880 http://dx.doi.org/10.1097/MD.0000000000002352 |
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author | Su, Vincent Yi-Fong Yen, Yung-Feng Pan, Sheng-Wei Chuang, Pei-Hung Feng, Jia-Yih Chou, Kun-Ta Chen, Yuh-Min Chen, Tzeng-Ji Su, Wei-Juin |
author_facet | Su, Vincent Yi-Fong Yen, Yung-Feng Pan, Sheng-Wei Chuang, Pei-Hung Feng, Jia-Yih Chou, Kun-Ta Chen, Yuh-Min Chen, Tzeng-Ji Su, Wei-Juin |
author_sort | Su, Vincent Yi-Fong |
collection | PubMed |
description | The association of latent tuberculosis infection (LTBI) with subsequent cancer remains unclear. We investigated the risk of future cancer among tuberculosis (TB) contacts with or without subsequent TB activation. Using the Taiwan National Health Insurance Research Database, we conducted a nationwide population-based study. TB contacts during 1997 to 2012 were included as the study cohort. Patients with antecedent cancer and TB were excluded. Data from 11,522 TB contacts and 46,088 age-, sex-, and enrollment date–matched subjects during 1997 to 2012 were analyzed. The 2 cohorts were monitored until December 31, 2012 for incidence of cancer and TB infection. LTBI was defined as a TB contact with subsequent TB activation. The primary endpoint was occurrence of newly diagnosed cancer. There was no difference in cancer development between the TB contact cohort and comparison cohort (log-rank test, P = 0.714). After multivariate adjustment, the hazard ratio (HR) for cancer among the LTBI patients was 2.29 [95% confidence interval (CI), 1.26–4.17; P = 0.007]. There was increase in cancer incidences for several specific cancer types, including multiple myeloma (HR 340.28), lung (HR 2.69), kidney and bladder (HR 6.16), hepatobiliary (HR 2.36), and gastrointestinal (HR 2.99) cancers. None of the 136 TB contacts who received isoniazid prophylaxis developed cancer. LTBI patients had a higher risk of future cancer. |
format | Online Article Text |
id | pubmed-5291550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-52915502017-02-09 Latent Tuberculosis Infection and the Risk of Subsequent Cancer Su, Vincent Yi-Fong Yen, Yung-Feng Pan, Sheng-Wei Chuang, Pei-Hung Feng, Jia-Yih Chou, Kun-Ta Chen, Yuh-Min Chen, Tzeng-Ji Su, Wei-Juin Medicine (Baltimore) 4900 The association of latent tuberculosis infection (LTBI) with subsequent cancer remains unclear. We investigated the risk of future cancer among tuberculosis (TB) contacts with or without subsequent TB activation. Using the Taiwan National Health Insurance Research Database, we conducted a nationwide population-based study. TB contacts during 1997 to 2012 were included as the study cohort. Patients with antecedent cancer and TB were excluded. Data from 11,522 TB contacts and 46,088 age-, sex-, and enrollment date–matched subjects during 1997 to 2012 were analyzed. The 2 cohorts were monitored until December 31, 2012 for incidence of cancer and TB infection. LTBI was defined as a TB contact with subsequent TB activation. The primary endpoint was occurrence of newly diagnosed cancer. There was no difference in cancer development between the TB contact cohort and comparison cohort (log-rank test, P = 0.714). After multivariate adjustment, the hazard ratio (HR) for cancer among the LTBI patients was 2.29 [95% confidence interval (CI), 1.26–4.17; P = 0.007]. There was increase in cancer incidences for several specific cancer types, including multiple myeloma (HR 340.28), lung (HR 2.69), kidney and bladder (HR 6.16), hepatobiliary (HR 2.36), and gastrointestinal (HR 2.99) cancers. None of the 136 TB contacts who received isoniazid prophylaxis developed cancer. LTBI patients had a higher risk of future cancer. Wolters Kluwer Health 2016-01-29 /pmc/articles/PMC5291550/ /pubmed/26825880 http://dx.doi.org/10.1097/MD.0000000000002352 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial License, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be used commercially. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 4900 Su, Vincent Yi-Fong Yen, Yung-Feng Pan, Sheng-Wei Chuang, Pei-Hung Feng, Jia-Yih Chou, Kun-Ta Chen, Yuh-Min Chen, Tzeng-Ji Su, Wei-Juin Latent Tuberculosis Infection and the Risk of Subsequent Cancer |
title | Latent Tuberculosis Infection and the Risk of Subsequent Cancer |
title_full | Latent Tuberculosis Infection and the Risk of Subsequent Cancer |
title_fullStr | Latent Tuberculosis Infection and the Risk of Subsequent Cancer |
title_full_unstemmed | Latent Tuberculosis Infection and the Risk of Subsequent Cancer |
title_short | Latent Tuberculosis Infection and the Risk of Subsequent Cancer |
title_sort | latent tuberculosis infection and the risk of subsequent cancer |
topic | 4900 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291550/ https://www.ncbi.nlm.nih.gov/pubmed/26825880 http://dx.doi.org/10.1097/MD.0000000000002352 |
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