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Aspirin Use and Risk of Hepatocellular Carcinoma in a National Cohort Study of Korean Adults
The effect of aspirin on the risk of hepatocellular carcinoma (HCC) remains unclear. We investigated the association between aspirin use and HCC development in a region where viral hepatitis prevails. We conducted a population-based cohort study including a total of 460,755 participants who were tra...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862896/ https://www.ncbi.nlm.nih.gov/pubmed/29563592 http://dx.doi.org/10.1038/s41598-018-23343-0 |
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author | Hwang, In Cheol Chang, Jooyoung Kim, Kyuwoong Park, Sang Min |
author_facet | Hwang, In Cheol Chang, Jooyoung Kim, Kyuwoong Park, Sang Min |
author_sort | Hwang, In Cheol |
collection | PubMed |
description | The effect of aspirin on the risk of hepatocellular carcinoma (HCC) remains unclear. We investigated the association between aspirin use and HCC development in a region where viral hepatitis prevails. We conducted a population-based cohort study including a total of 460,755 participants who were tracked to identify incidents of HCC since 2007. The use of drug before the index date was assessed and standardized by the Defined Daily Dose system. We calculated the hazard ratios (HRs) and their 95% confidence intervals (CIs) for the association between aspirin use and HCC occurrence, using Cox proportional hazard regression models. There were 2,336 cases of HCC during the period of 2,965,500 person-years. Overall, aspirin users had a lower HCC risk (HR, 0.87; 95% CI, 0.77–0.98) than non-users in a dose-response manner (P(trend) = 0.002). The protective effect of aspirin was amplified when combined with those of non-aspirin non-steroidal anti-inflammatory drugs (HR, 0.65; 95% CI, 0.50–0.85). Subgroup analyses revealed a significant chemopreventive effect of aspirin in individuals who were young, were male, or had viral hepatitis, whereas no protective effect was observed in patients with liver cirrhosis. Our results, suggesting different carcinogenic pathways between viral and non-viral etiologies, may validate the design of future intervention trials of aspirin for HCC prevention in eligible populations. |
format | Online Article Text |
id | pubmed-5862896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58628962018-03-27 Aspirin Use and Risk of Hepatocellular Carcinoma in a National Cohort Study of Korean Adults Hwang, In Cheol Chang, Jooyoung Kim, Kyuwoong Park, Sang Min Sci Rep Article The effect of aspirin on the risk of hepatocellular carcinoma (HCC) remains unclear. We investigated the association between aspirin use and HCC development in a region where viral hepatitis prevails. We conducted a population-based cohort study including a total of 460,755 participants who were tracked to identify incidents of HCC since 2007. The use of drug before the index date was assessed and standardized by the Defined Daily Dose system. We calculated the hazard ratios (HRs) and their 95% confidence intervals (CIs) for the association between aspirin use and HCC occurrence, using Cox proportional hazard regression models. There were 2,336 cases of HCC during the period of 2,965,500 person-years. Overall, aspirin users had a lower HCC risk (HR, 0.87; 95% CI, 0.77–0.98) than non-users in a dose-response manner (P(trend) = 0.002). The protective effect of aspirin was amplified when combined with those of non-aspirin non-steroidal anti-inflammatory drugs (HR, 0.65; 95% CI, 0.50–0.85). Subgroup analyses revealed a significant chemopreventive effect of aspirin in individuals who were young, were male, or had viral hepatitis, whereas no protective effect was observed in patients with liver cirrhosis. Our results, suggesting different carcinogenic pathways between viral and non-viral etiologies, may validate the design of future intervention trials of aspirin for HCC prevention in eligible populations. Nature Publishing Group UK 2018-03-21 /pmc/articles/PMC5862896/ /pubmed/29563592 http://dx.doi.org/10.1038/s41598-018-23343-0 Text en © The Author(s) 2018 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 Hwang, In Cheol Chang, Jooyoung Kim, Kyuwoong Park, Sang Min Aspirin Use and Risk of Hepatocellular Carcinoma in a National Cohort Study of Korean Adults |
title | Aspirin Use and Risk of Hepatocellular Carcinoma in a National Cohort Study of Korean Adults |
title_full | Aspirin Use and Risk of Hepatocellular Carcinoma in a National Cohort Study of Korean Adults |
title_fullStr | Aspirin Use and Risk of Hepatocellular Carcinoma in a National Cohort Study of Korean Adults |
title_full_unstemmed | Aspirin Use and Risk of Hepatocellular Carcinoma in a National Cohort Study of Korean Adults |
title_short | Aspirin Use and Risk of Hepatocellular Carcinoma in a National Cohort Study of Korean Adults |
title_sort | aspirin use and risk of hepatocellular carcinoma in a national cohort study of korean adults |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5862896/ https://www.ncbi.nlm.nih.gov/pubmed/29563592 http://dx.doi.org/10.1038/s41598-018-23343-0 |
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