Cargando…
Aspirin and the risk of hepatocellular carcinoma development in patients with alcoholic cirrhosis
Aspirin therapy has shown protective effects against hepatocellular carcinoma (HCC) in preclinical studies. However, it is unclear whether aspirin therapy lowers the risk of HCC in patients with alcoholic cirrhosis. A retrospective analysis of data from 949 consecutive patients with alcoholic cirrho...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478404/ https://www.ncbi.nlm.nih.gov/pubmed/32118712 http://dx.doi.org/10.1097/MD.0000000000019008 |
_version_ | 1783580043290607616 |
---|---|
author | Shin, Sangdeok Lee, Sang Hoon Lee, Minjong Kim, Ji Hyun Lee, Wongu Lee, Hyun Woo Park, Min Soo Park, Seungwoo Kim, Tae Suk Choi, Dae Hee |
author_facet | Shin, Sangdeok Lee, Sang Hoon Lee, Minjong Kim, Ji Hyun Lee, Wongu Lee, Hyun Woo Park, Min Soo Park, Seungwoo Kim, Tae Suk Choi, Dae Hee |
author_sort | Shin, Sangdeok |
collection | PubMed |
description | Aspirin therapy has shown protective effects against hepatocellular carcinoma (HCC) in preclinical studies. However, it is unclear whether aspirin therapy lowers the risk of HCC in patients with alcoholic cirrhosis. A retrospective analysis of data from 949 consecutive patients with alcoholic cirrhosis who abstained from alcoholic drinking was performed. The primary and secondary outcomes were development of HCC and gastrointestinal bleeding events, respectively. Risk was compared between patients with aspirin treatment and patients who were not treated (non-aspirin group) using a time-varying Cox proportional hazards model for total population and propensity score-matching analysis. The aspirin group included 224 patients and the non-aspirin group had 725 patients. During the study period of median duration of 3.1 years, 133 patients (13.6%) developed HCC. In time-varying Cox proportional analyses, the aspirin group showed a significantly lower risk of HCC (adjusted hazard ratio [aHR]: 0.13; 95% confidence interval [CI]: 0.08–0.21; P < .001). In propensity score-matched pairs, aspirin therapy significantly reduced the risk of HCC (aHR: 0.14; 95% CI: 0.09–0.22; P < .001). In bleeding risk, treatment with aspirin alone was not significantly associated with a higher bleeding risk (aHR: 0.81; 95% CI: 0.45–1.44; P = .46). Aspirin therapy was associated with the lower risk of HCC in patients with alcoholic cirrhosis. |
format | Online Article Text |
id | pubmed-7478404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-74784042020-09-16 Aspirin and the risk of hepatocellular carcinoma development in patients with alcoholic cirrhosis Shin, Sangdeok Lee, Sang Hoon Lee, Minjong Kim, Ji Hyun Lee, Wongu Lee, Hyun Woo Park, Min Soo Park, Seungwoo Kim, Tae Suk Choi, Dae Hee Medicine (Baltimore) 4500 Aspirin therapy has shown protective effects against hepatocellular carcinoma (HCC) in preclinical studies. However, it is unclear whether aspirin therapy lowers the risk of HCC in patients with alcoholic cirrhosis. A retrospective analysis of data from 949 consecutive patients with alcoholic cirrhosis who abstained from alcoholic drinking was performed. The primary and secondary outcomes were development of HCC and gastrointestinal bleeding events, respectively. Risk was compared between patients with aspirin treatment and patients who were not treated (non-aspirin group) using a time-varying Cox proportional hazards model for total population and propensity score-matching analysis. The aspirin group included 224 patients and the non-aspirin group had 725 patients. During the study period of median duration of 3.1 years, 133 patients (13.6%) developed HCC. In time-varying Cox proportional analyses, the aspirin group showed a significantly lower risk of HCC (adjusted hazard ratio [aHR]: 0.13; 95% confidence interval [CI]: 0.08–0.21; P < .001). In propensity score-matched pairs, aspirin therapy significantly reduced the risk of HCC (aHR: 0.14; 95% CI: 0.09–0.22; P < .001). In bleeding risk, treatment with aspirin alone was not significantly associated with a higher bleeding risk (aHR: 0.81; 95% CI: 0.45–1.44; P = .46). Aspirin therapy was associated with the lower risk of HCC in patients with alcoholic cirrhosis. Wolters Kluwer Health 2020-02-28 /pmc/articles/PMC7478404/ /pubmed/32118712 http://dx.doi.org/10.1097/MD.0000000000019008 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 4500 Shin, Sangdeok Lee, Sang Hoon Lee, Minjong Kim, Ji Hyun Lee, Wongu Lee, Hyun Woo Park, Min Soo Park, Seungwoo Kim, Tae Suk Choi, Dae Hee Aspirin and the risk of hepatocellular carcinoma development in patients with alcoholic cirrhosis |
title | Aspirin and the risk of hepatocellular carcinoma development in patients with alcoholic cirrhosis |
title_full | Aspirin and the risk of hepatocellular carcinoma development in patients with alcoholic cirrhosis |
title_fullStr | Aspirin and the risk of hepatocellular carcinoma development in patients with alcoholic cirrhosis |
title_full_unstemmed | Aspirin and the risk of hepatocellular carcinoma development in patients with alcoholic cirrhosis |
title_short | Aspirin and the risk of hepatocellular carcinoma development in patients with alcoholic cirrhosis |
title_sort | aspirin and the risk of hepatocellular carcinoma development in patients with alcoholic cirrhosis |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478404/ https://www.ncbi.nlm.nih.gov/pubmed/32118712 http://dx.doi.org/10.1097/MD.0000000000019008 |
work_keys_str_mv | AT shinsangdeok aspirinandtheriskofhepatocellularcarcinomadevelopmentinpatientswithalcoholiccirrhosis AT leesanghoon aspirinandtheriskofhepatocellularcarcinomadevelopmentinpatientswithalcoholiccirrhosis AT leeminjong aspirinandtheriskofhepatocellularcarcinomadevelopmentinpatientswithalcoholiccirrhosis AT kimjihyun aspirinandtheriskofhepatocellularcarcinomadevelopmentinpatientswithalcoholiccirrhosis AT leewongu aspirinandtheriskofhepatocellularcarcinomadevelopmentinpatientswithalcoholiccirrhosis AT leehyunwoo aspirinandtheriskofhepatocellularcarcinomadevelopmentinpatientswithalcoholiccirrhosis AT parkminsoo aspirinandtheriskofhepatocellularcarcinomadevelopmentinpatientswithalcoholiccirrhosis AT parkseungwoo aspirinandtheriskofhepatocellularcarcinomadevelopmentinpatientswithalcoholiccirrhosis AT kimtaesuk aspirinandtheriskofhepatocellularcarcinomadevelopmentinpatientswithalcoholiccirrhosis AT choidaehee aspirinandtheriskofhepatocellularcarcinomadevelopmentinpatientswithalcoholiccirrhosis |