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Amiodarone and risk of liver cirrhosis: a nationwide, population-based study
BACKGROUND: Liver cirrhosis is an uncommon but not rare side effect of amiodarone-induced hepatotoxicity. Patients with hepatitis B virus and hepatitis C virus infections are at a high risk for developing liver cirrhosis. However, the relationship between this treatment and risk of liver cirrhosis i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330968/ https://www.ncbi.nlm.nih.gov/pubmed/30666120 http://dx.doi.org/10.2147/TCRM.S174868 |
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author | Huang, Ching-Hui Lai, Ya-Yun Kuo, Yu-Jui Yang, Su-Ching Chang, Yu-Jun Chang, Kuo-Kuan Chen, Wen-Kang |
author_facet | Huang, Ching-Hui Lai, Ya-Yun Kuo, Yu-Jui Yang, Su-Ching Chang, Yu-Jun Chang, Kuo-Kuan Chen, Wen-Kang |
author_sort | Huang, Ching-Hui |
collection | PubMed |
description | BACKGROUND: Liver cirrhosis is an uncommon but not rare side effect of amiodarone-induced hepatotoxicity. Patients with hepatitis B virus and hepatitis C virus infections are at a high risk for developing liver cirrhosis. However, the relationship between this treatment and risk of liver cirrhosis in high-risk chronic hepatitis B and chronic hepatitis C patients is unknown. PATIENTS AND METHODS: The present study identified amiodarone users (N=8,081) from the Taiwan National Health Insurance Research Database from 1997 through 2013. A total of 32,324 subjects with age, comorbidities, gender, and index date-matched non-amiodarone users were selected as controls (non-amiodarone cohort). The incidences of cumulative liver cirrhosis were compared between cohorts. Stratified Cox’s regression hazard models were used to assess possible comorbidity-attributable risks for liver cirrhosis. RESULTS: The amiodarone cohort had a nonsignificant risk of liver cirrhosis compared with the non-amiodarone cohort, with a HR of 1.17 (95% CI: 0.93–1.47; P=0.1723). Patients with specific comorbid diseases, including type 2 diabetes mellitus, chronic hepatitis B, chronic hepatitis C, and heart failure, were probably at a high risk of developing liver cirrhosis. The use of statins was associated with a significant 42% reduction in the risk of liver cirrhosis. CONCLUSION: Patients in the amiodarone cohort had no excess risk of liver cirrhosis compared with patients in the non-amiodarone cohort. Long-term surveillance for liver toxicity in high-risk patients with amiodarone treatment is suggested. |
format | Online Article Text |
id | pubmed-6330968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63309682019-01-21 Amiodarone and risk of liver cirrhosis: a nationwide, population-based study Huang, Ching-Hui Lai, Ya-Yun Kuo, Yu-Jui Yang, Su-Ching Chang, Yu-Jun Chang, Kuo-Kuan Chen, Wen-Kang Ther Clin Risk Manag Original Research BACKGROUND: Liver cirrhosis is an uncommon but not rare side effect of amiodarone-induced hepatotoxicity. Patients with hepatitis B virus and hepatitis C virus infections are at a high risk for developing liver cirrhosis. However, the relationship between this treatment and risk of liver cirrhosis in high-risk chronic hepatitis B and chronic hepatitis C patients is unknown. PATIENTS AND METHODS: The present study identified amiodarone users (N=8,081) from the Taiwan National Health Insurance Research Database from 1997 through 2013. A total of 32,324 subjects with age, comorbidities, gender, and index date-matched non-amiodarone users were selected as controls (non-amiodarone cohort). The incidences of cumulative liver cirrhosis were compared between cohorts. Stratified Cox’s regression hazard models were used to assess possible comorbidity-attributable risks for liver cirrhosis. RESULTS: The amiodarone cohort had a nonsignificant risk of liver cirrhosis compared with the non-amiodarone cohort, with a HR of 1.17 (95% CI: 0.93–1.47; P=0.1723). Patients with specific comorbid diseases, including type 2 diabetes mellitus, chronic hepatitis B, chronic hepatitis C, and heart failure, were probably at a high risk of developing liver cirrhosis. The use of statins was associated with a significant 42% reduction in the risk of liver cirrhosis. CONCLUSION: Patients in the amiodarone cohort had no excess risk of liver cirrhosis compared with patients in the non-amiodarone cohort. Long-term surveillance for liver toxicity in high-risk patients with amiodarone treatment is suggested. Dove Medical Press 2019-01-10 /pmc/articles/PMC6330968/ /pubmed/30666120 http://dx.doi.org/10.2147/TCRM.S174868 Text en © 2019 Huang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Huang, Ching-Hui Lai, Ya-Yun Kuo, Yu-Jui Yang, Su-Ching Chang, Yu-Jun Chang, Kuo-Kuan Chen, Wen-Kang Amiodarone and risk of liver cirrhosis: a nationwide, population-based study |
title | Amiodarone and risk of liver cirrhosis: a nationwide, population-based study |
title_full | Amiodarone and risk of liver cirrhosis: a nationwide, population-based study |
title_fullStr | Amiodarone and risk of liver cirrhosis: a nationwide, population-based study |
title_full_unstemmed | Amiodarone and risk of liver cirrhosis: a nationwide, population-based study |
title_short | Amiodarone and risk of liver cirrhosis: a nationwide, population-based study |
title_sort | amiodarone and risk of liver cirrhosis: a nationwide, population-based study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330968/ https://www.ncbi.nlm.nih.gov/pubmed/30666120 http://dx.doi.org/10.2147/TCRM.S174868 |
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