Cargando…

Association Between Nonselective Beta-Blocker Use and Hepatocellular Carcinoma in Patients With Chronic Hepatitis B Without Cirrhosis and Decompensation

Background: Nonselective beta-blockers (NSBBs) can reduce the incidence or mortality of certain types of cancers, and NSBBs exert a protective effect on hepatocellular carcinoma (HCC) in patients with cirrhosis. However, the potential preventive effect of NSBBs has not yet been investigated in patie...

Descripción completa

Detalles Bibliográficos
Autores principales: Cheng, He-Yun, Lin, Hsiu C., Lin, Hsiu L., Uang, Yow S., Keller, Joseph J., Wang, Li H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777254/
https://www.ncbi.nlm.nih.gov/pubmed/35069216
http://dx.doi.org/10.3389/fphar.2021.805318
_version_ 1784637026236104704
author Cheng, He-Yun
Lin, Hsiu C.
Lin, Hsiu L.
Uang, Yow S.
Keller, Joseph J.
Wang, Li H.
author_facet Cheng, He-Yun
Lin, Hsiu C.
Lin, Hsiu L.
Uang, Yow S.
Keller, Joseph J.
Wang, Li H.
author_sort Cheng, He-Yun
collection PubMed
description Background: Nonselective beta-blockers (NSBBs) can reduce the incidence or mortality of certain types of cancers, and NSBBs exert a protective effect on hepatocellular carcinoma (HCC) in patients with cirrhosis. However, the potential preventive effect of NSBBs has not yet been investigated in patients with chronic hepatitis B (CHB) who have a high HCC risk regardless of the presence of underlying cirrhosis. Aim: This study evaluated the association between NSBB use and HCC incidence in patients with CHB without cirrhosis and decompensation. Methods: From the 2000 Longitudinal Generation Tracking Database, we enrolled patients who were newly diagnosed as having CHB from January 2001 to December 2011 and then followed them up for at least 5 years. To estimate the causal effect of NSBBs on the time-to-event outcomes of HCC, a marginal Cox proportional hazards model was used to calculate hazard ratios (HRs) and 95% confidence intervals (CIs). Results: After adjustment, no significant benefit of HCC risk reduction was observed between the NSBB users and nonusers (adjusted HR, 0.82; 95% CI, 0.52–1.31). The cumulative defined daily dose (cDDD) analysis revealed no significant dose correlation among the three groups [adjusted HR (95% CI): 1.08, (0.56–2.05), 0.54 (0.17–1.77), and 0.76 (0.40–1.42) in the <90 cDDD, 90 to <180 cDDD, and ≥180 cDDD groups, respectively]. Duration-dependent associations were not observed. Multivariable stratified analysis results demonstrated that HCC risk markedly decreased in the patients aged >55 years (adjusted HR, 0.49; 95% CI, 0.25–0.96; p = 0.04). Conclusion: NSBB did not significantly prevent HCC in the patients with CHB infection without cirrhosis and decompensation. This study provided one of valuable results that it is not clinically required to use NSBBs as recommended chemoprevention for HCC in high-risk patients who have CHB.
format Online
Article
Text
id pubmed-8777254
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-87772542022-01-22 Association Between Nonselective Beta-Blocker Use and Hepatocellular Carcinoma in Patients With Chronic Hepatitis B Without Cirrhosis and Decompensation Cheng, He-Yun Lin, Hsiu C. Lin, Hsiu L. Uang, Yow S. Keller, Joseph J. Wang, Li H. Front Pharmacol Pharmacology Background: Nonselective beta-blockers (NSBBs) can reduce the incidence or mortality of certain types of cancers, and NSBBs exert a protective effect on hepatocellular carcinoma (HCC) in patients with cirrhosis. However, the potential preventive effect of NSBBs has not yet been investigated in patients with chronic hepatitis B (CHB) who have a high HCC risk regardless of the presence of underlying cirrhosis. Aim: This study evaluated the association between NSBB use and HCC incidence in patients with CHB without cirrhosis and decompensation. Methods: From the 2000 Longitudinal Generation Tracking Database, we enrolled patients who were newly diagnosed as having CHB from January 2001 to December 2011 and then followed them up for at least 5 years. To estimate the causal effect of NSBBs on the time-to-event outcomes of HCC, a marginal Cox proportional hazards model was used to calculate hazard ratios (HRs) and 95% confidence intervals (CIs). Results: After adjustment, no significant benefit of HCC risk reduction was observed between the NSBB users and nonusers (adjusted HR, 0.82; 95% CI, 0.52–1.31). The cumulative defined daily dose (cDDD) analysis revealed no significant dose correlation among the three groups [adjusted HR (95% CI): 1.08, (0.56–2.05), 0.54 (0.17–1.77), and 0.76 (0.40–1.42) in the <90 cDDD, 90 to <180 cDDD, and ≥180 cDDD groups, respectively]. Duration-dependent associations were not observed. Multivariable stratified analysis results demonstrated that HCC risk markedly decreased in the patients aged >55 years (adjusted HR, 0.49; 95% CI, 0.25–0.96; p = 0.04). Conclusion: NSBB did not significantly prevent HCC in the patients with CHB infection without cirrhosis and decompensation. This study provided one of valuable results that it is not clinically required to use NSBBs as recommended chemoprevention for HCC in high-risk patients who have CHB. Frontiers Media S.A. 2022-01-07 /pmc/articles/PMC8777254/ /pubmed/35069216 http://dx.doi.org/10.3389/fphar.2021.805318 Text en Copyright © 2022 Cheng, Lin, Lin, Uang, Keller and Wang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Cheng, He-Yun
Lin, Hsiu C.
Lin, Hsiu L.
Uang, Yow S.
Keller, Joseph J.
Wang, Li H.
Association Between Nonselective Beta-Blocker Use and Hepatocellular Carcinoma in Patients With Chronic Hepatitis B Without Cirrhosis and Decompensation
title Association Between Nonselective Beta-Blocker Use and Hepatocellular Carcinoma in Patients With Chronic Hepatitis B Without Cirrhosis and Decompensation
title_full Association Between Nonselective Beta-Blocker Use and Hepatocellular Carcinoma in Patients With Chronic Hepatitis B Without Cirrhosis and Decompensation
title_fullStr Association Between Nonselective Beta-Blocker Use and Hepatocellular Carcinoma in Patients With Chronic Hepatitis B Without Cirrhosis and Decompensation
title_full_unstemmed Association Between Nonselective Beta-Blocker Use and Hepatocellular Carcinoma in Patients With Chronic Hepatitis B Without Cirrhosis and Decompensation
title_short Association Between Nonselective Beta-Blocker Use and Hepatocellular Carcinoma in Patients With Chronic Hepatitis B Without Cirrhosis and Decompensation
title_sort association between nonselective beta-blocker use and hepatocellular carcinoma in patients with chronic hepatitis b without cirrhosis and decompensation
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8777254/
https://www.ncbi.nlm.nih.gov/pubmed/35069216
http://dx.doi.org/10.3389/fphar.2021.805318
work_keys_str_mv AT chengheyun associationbetweennonselectivebetablockeruseandhepatocellularcarcinomainpatientswithchronichepatitisbwithoutcirrhosisanddecompensation
AT linhsiuc associationbetweennonselectivebetablockeruseandhepatocellularcarcinomainpatientswithchronichepatitisbwithoutcirrhosisanddecompensation
AT linhsiul associationbetweennonselectivebetablockeruseandhepatocellularcarcinomainpatientswithchronichepatitisbwithoutcirrhosisanddecompensation
AT uangyows associationbetweennonselectivebetablockeruseandhepatocellularcarcinomainpatientswithchronichepatitisbwithoutcirrhosisanddecompensation
AT kellerjosephj associationbetweennonselectivebetablockeruseandhepatocellularcarcinomainpatientswithchronichepatitisbwithoutcirrhosisanddecompensation
AT wanglih associationbetweennonselectivebetablockeruseandhepatocellularcarcinomainpatientswithchronichepatitisbwithoutcirrhosisanddecompensation