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Interaction and joint effect of ALT and chronic liver disease on liver cancer in type 2 diabetes patients

BACKGROUND: This study examined whether serum alanine transaminase (ALT) and chronic liver diseases were interactively, jointly, or independently associated with hepatocellular carcinoma (HCC) risk in type 2 diabetic patients. MATERIALS AND METHODS: A retrospective cohort study was conducted in 46,3...

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Autores principales: Li, Tsai-Chung, Li, Chia-Ing, Liu, Chiu-Shong, Lin, Pao-Hsuan, Lin, Wen-Yuan, Lin, Chih-Hsueh, Yang, Sing-Yu, Chiang, Jen-Huai, Lin, Cheng-Chieh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732771/
https://www.ncbi.nlm.nih.gov/pubmed/29262605
http://dx.doi.org/10.18632/oncotarget.21804
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author Li, Tsai-Chung
Li, Chia-Ing
Liu, Chiu-Shong
Lin, Pao-Hsuan
Lin, Wen-Yuan
Lin, Chih-Hsueh
Yang, Sing-Yu
Chiang, Jen-Huai
Lin, Cheng-Chieh
author_facet Li, Tsai-Chung
Li, Chia-Ing
Liu, Chiu-Shong
Lin, Pao-Hsuan
Lin, Wen-Yuan
Lin, Chih-Hsueh
Yang, Sing-Yu
Chiang, Jen-Huai
Lin, Cheng-Chieh
author_sort Li, Tsai-Chung
collection PubMed
description BACKGROUND: This study examined whether serum alanine transaminase (ALT) and chronic liver diseases were interactively, jointly, or independently associated with hepatocellular carcinoma (HCC) risk in type 2 diabetic patients. MATERIALS AND METHODS: A retrospective cohort study was conducted in 46,369 Chinese type 2 diabetic patients, aged 30 and older, in National Diabetes Care Management Program in 2002-2004. These data were analyzed by multivariate Cox proportional hazards models. RESULTS: Mean follow-up period was 8.20 years. Multivariate-adjusted hazard ratios of HCC were 2.85 (95% confidence interval, CI: 2.45–3.31), 3.80 (3.04–4.76), and 3.89 (3.08–4.91) for patients with a level of ALT 40–80, 80–120, and >120 U/L, respectively, compared with patients with a level of ALT < 40 U/L after multivariable adjustment. Significant hazard ratios of HCC for patients with a level of ALT ≥ 40 U/L and alcoholic liver damage, nonalcoholic fatty liver disease, liver cirrhosis, hepatitis B virus and hepatitis C virus infection, or any one of these chronic liver diseases compared with patients with ALT level < 40 U/L and no counterpart comorbidity were observed. Significant effect modifications were observed between ALT level with liver cirrhosis and HBV. CONCLUSIONS: Results suggest significant effect modification and joint associations of ALT ≥ 40 U/L and chronic liver diseases. Diabetes care should provide lifestyle or treatment interventions to manage ALT level, liver cirrhosis and hepatitis B virus infection for reducing burden of HCC.
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spelling pubmed-57327712017-12-19 Interaction and joint effect of ALT and chronic liver disease on liver cancer in type 2 diabetes patients Li, Tsai-Chung Li, Chia-Ing Liu, Chiu-Shong Lin, Pao-Hsuan Lin, Wen-Yuan Lin, Chih-Hsueh Yang, Sing-Yu Chiang, Jen-Huai Lin, Cheng-Chieh Oncotarget Research Paper BACKGROUND: This study examined whether serum alanine transaminase (ALT) and chronic liver diseases were interactively, jointly, or independently associated with hepatocellular carcinoma (HCC) risk in type 2 diabetic patients. MATERIALS AND METHODS: A retrospective cohort study was conducted in 46,369 Chinese type 2 diabetic patients, aged 30 and older, in National Diabetes Care Management Program in 2002-2004. These data were analyzed by multivariate Cox proportional hazards models. RESULTS: Mean follow-up period was 8.20 years. Multivariate-adjusted hazard ratios of HCC were 2.85 (95% confidence interval, CI: 2.45–3.31), 3.80 (3.04–4.76), and 3.89 (3.08–4.91) for patients with a level of ALT 40–80, 80–120, and >120 U/L, respectively, compared with patients with a level of ALT < 40 U/L after multivariable adjustment. Significant hazard ratios of HCC for patients with a level of ALT ≥ 40 U/L and alcoholic liver damage, nonalcoholic fatty liver disease, liver cirrhosis, hepatitis B virus and hepatitis C virus infection, or any one of these chronic liver diseases compared with patients with ALT level < 40 U/L and no counterpart comorbidity were observed. Significant effect modifications were observed between ALT level with liver cirrhosis and HBV. CONCLUSIONS: Results suggest significant effect modification and joint associations of ALT ≥ 40 U/L and chronic liver diseases. Diabetes care should provide lifestyle or treatment interventions to manage ALT level, liver cirrhosis and hepatitis B virus infection for reducing burden of HCC. Impact Journals LLC 2017-10-10 /pmc/articles/PMC5732771/ /pubmed/29262605 http://dx.doi.org/10.18632/oncotarget.21804 Text en Copyright: © 2017 Li et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Li, Tsai-Chung
Li, Chia-Ing
Liu, Chiu-Shong
Lin, Pao-Hsuan
Lin, Wen-Yuan
Lin, Chih-Hsueh
Yang, Sing-Yu
Chiang, Jen-Huai
Lin, Cheng-Chieh
Interaction and joint effect of ALT and chronic liver disease on liver cancer in type 2 diabetes patients
title Interaction and joint effect of ALT and chronic liver disease on liver cancer in type 2 diabetes patients
title_full Interaction and joint effect of ALT and chronic liver disease on liver cancer in type 2 diabetes patients
title_fullStr Interaction and joint effect of ALT and chronic liver disease on liver cancer in type 2 diabetes patients
title_full_unstemmed Interaction and joint effect of ALT and chronic liver disease on liver cancer in type 2 diabetes patients
title_short Interaction and joint effect of ALT and chronic liver disease on liver cancer in type 2 diabetes patients
title_sort interaction and joint effect of alt and chronic liver disease on liver cancer in type 2 diabetes patients
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5732771/
https://www.ncbi.nlm.nih.gov/pubmed/29262605
http://dx.doi.org/10.18632/oncotarget.21804
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