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Coffee consumption and risk of hepatocellular carcinoma: a meta-analysis of eleven epidemiological studies
Growing evidence has shown that coffee consumption is inversely related with the risk of hepatocellular carcinoma. It is suggested that caffeine maintains strong antioxidative activity. With this property, coffee intake may lead to the inhibition of cell proliferation of liver cancer cells; also, so...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959413/ https://www.ncbi.nlm.nih.gov/pubmed/27499631 http://dx.doi.org/10.2147/OTT.S109656 |
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author | Bai, Kai Cai, Qiucheng Jiang, Yi Lv, Lizhi |
author_facet | Bai, Kai Cai, Qiucheng Jiang, Yi Lv, Lizhi |
author_sort | Bai, Kai |
collection | PubMed |
description | Growing evidence has shown that coffee consumption is inversely related with the risk of hepatocellular carcinoma. It is suggested that caffeine maintains strong antioxidative activity. With this property, coffee intake may lead to the inhibition of cell proliferation of liver cancer cells; also, some compounds contained in coffee can reduce the genotoxicity of aflatoxin B1 in vitro and lower the damage caused by some carcinogens. A computerized search was performed in PubMed to identify relevant articles published before August 2015. Eleven relevant studies were included with a total of 2,795 cases and 340,749 control subjects. According to the meta-analysis we performed, the pooled odds ratio (OR) from all included studies was 0.49 (95% confidence interval [CI] =0.46–0.52). The subgroup analysis indicated that the pooled ORs for Asian studies and other populations were 0.27 (95% CI =0.23–0.31) and 0.82 (95% CI =0.77–0.87), respectively. The overall pooled OR for high consumption was decreased to 0.21 (95% CI =0.18–0.25) and significance was observed. Among other populations, the pooled OR of subjects with high coffee consumption was 0.65 (95% CI =0.56–0.73) compared to the nondrinker. The corresponding OR of five Asian studies was 0.13 (95% CI =0.09–0.17). The findings from this meta-analysis further confirmed the inverse association between the coffee consumption and hepatocellular carcinoma risk with quantitative evidence. The protective effect can be detected among healthy population and patients with chronic liver diseases, and the consumption can also prevent the development of liver cirrhosis. |
format | Online Article Text |
id | pubmed-4959413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-49594132016-08-05 Coffee consumption and risk of hepatocellular carcinoma: a meta-analysis of eleven epidemiological studies Bai, Kai Cai, Qiucheng Jiang, Yi Lv, Lizhi Onco Targets Ther Original Research Growing evidence has shown that coffee consumption is inversely related with the risk of hepatocellular carcinoma. It is suggested that caffeine maintains strong antioxidative activity. With this property, coffee intake may lead to the inhibition of cell proliferation of liver cancer cells; also, some compounds contained in coffee can reduce the genotoxicity of aflatoxin B1 in vitro and lower the damage caused by some carcinogens. A computerized search was performed in PubMed to identify relevant articles published before August 2015. Eleven relevant studies were included with a total of 2,795 cases and 340,749 control subjects. According to the meta-analysis we performed, the pooled odds ratio (OR) from all included studies was 0.49 (95% confidence interval [CI] =0.46–0.52). The subgroup analysis indicated that the pooled ORs for Asian studies and other populations were 0.27 (95% CI =0.23–0.31) and 0.82 (95% CI =0.77–0.87), respectively. The overall pooled OR for high consumption was decreased to 0.21 (95% CI =0.18–0.25) and significance was observed. Among other populations, the pooled OR of subjects with high coffee consumption was 0.65 (95% CI =0.56–0.73) compared to the nondrinker. The corresponding OR of five Asian studies was 0.13 (95% CI =0.09–0.17). The findings from this meta-analysis further confirmed the inverse association between the coffee consumption and hepatocellular carcinoma risk with quantitative evidence. The protective effect can be detected among healthy population and patients with chronic liver diseases, and the consumption can also prevent the development of liver cirrhosis. Dove Medical Press 2016-07-19 /pmc/articles/PMC4959413/ /pubmed/27499631 http://dx.doi.org/10.2147/OTT.S109656 Text en © 2016 Bai 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 Bai, Kai Cai, Qiucheng Jiang, Yi Lv, Lizhi Coffee consumption and risk of hepatocellular carcinoma: a meta-analysis of eleven epidemiological studies |
title | Coffee consumption and risk of hepatocellular carcinoma: a meta-analysis of eleven epidemiological studies |
title_full | Coffee consumption and risk of hepatocellular carcinoma: a meta-analysis of eleven epidemiological studies |
title_fullStr | Coffee consumption and risk of hepatocellular carcinoma: a meta-analysis of eleven epidemiological studies |
title_full_unstemmed | Coffee consumption and risk of hepatocellular carcinoma: a meta-analysis of eleven epidemiological studies |
title_short | Coffee consumption and risk of hepatocellular carcinoma: a meta-analysis of eleven epidemiological studies |
title_sort | coffee consumption and risk of hepatocellular carcinoma: a meta-analysis of eleven epidemiological studies |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959413/ https://www.ncbi.nlm.nih.gov/pubmed/27499631 http://dx.doi.org/10.2147/OTT.S109656 |
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