{"title":"Retrospective analysis of steatosis effect on antiviral response and hepatocellular carcinoma risk in chronic hepatitis C","authors":"Saptarshi Bhattacharyya , Ming-Lung Yu , Phumelele Yvonne Siphepho , Jee-Fu Huang , Chia-Yen Dai , Wan-Long Chuang , Shu-Chi Wang","doi":"10.1016/j.antiviral.2025.106203","DOIUrl":null,"url":null,"abstract":"<div><div>Hepatic steatosis is increasingly the leading cause of liver disease and suboptimal virologic response in chronic hepatitis C virus (CHC) infections worldwide. In Taiwan, the prevalence of cirrhosis and liver disease among CHC patients with steatosis has surged, influenced mainly by Westernized dietary habits. This retrospective study aimed to assess how varying degrees of hepatic steatosis impact the severity of liver fibrosis and hepatocellular carcinoma (HCC) risk in CHC patients undergoing pegylated interferon (Peg-IFN) and ribavirin (RBV) treatment. We analyzed their treatment outcomes, HCC development, and baseline steatosis severity using Brunt's classification after 24 weeks of Peg-IFN/RBV treatment and a 14-year observation (2010–2024). Of 1121 CHC patients, 518 (46 %) had baseline steatosis. Patients with severe steatosis (S2/S3) were older, predominantly diabetic, and had higher fibrosis levels and BMI. Our data revealed that fibrosis was a significant risk factor, especially in mild steatosis cases. Among the cohort, 20 % developed HCC, with its incidence increasing with the degree of steatosis. Steatosis was notably prevalent in mild fibrosis cases. In conclusion, in CHC patients treated with IFN therapy, the steatosis degree directly correlated with fibrosis severity and HCC development. Notably, baseline steatosis emerged as a risk factor in patients showcasing mild liver fibrosis.</div></div>","PeriodicalId":8259,"journal":{"name":"Antiviral research","volume":"240 ","pages":"Article 106203"},"PeriodicalIF":4.5000,"publicationDate":"2025-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Antiviral research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0166354225001299","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0
Abstract
Hepatic steatosis is increasingly the leading cause of liver disease and suboptimal virologic response in chronic hepatitis C virus (CHC) infections worldwide. In Taiwan, the prevalence of cirrhosis and liver disease among CHC patients with steatosis has surged, influenced mainly by Westernized dietary habits. This retrospective study aimed to assess how varying degrees of hepatic steatosis impact the severity of liver fibrosis and hepatocellular carcinoma (HCC) risk in CHC patients undergoing pegylated interferon (Peg-IFN) and ribavirin (RBV) treatment. We analyzed their treatment outcomes, HCC development, and baseline steatosis severity using Brunt's classification after 24 weeks of Peg-IFN/RBV treatment and a 14-year observation (2010–2024). Of 1121 CHC patients, 518 (46 %) had baseline steatosis. Patients with severe steatosis (S2/S3) were older, predominantly diabetic, and had higher fibrosis levels and BMI. Our data revealed that fibrosis was a significant risk factor, especially in mild steatosis cases. Among the cohort, 20 % developed HCC, with its incidence increasing with the degree of steatosis. Steatosis was notably prevalent in mild fibrosis cases. In conclusion, in CHC patients treated with IFN therapy, the steatosis degree directly correlated with fibrosis severity and HCC development. Notably, baseline steatosis emerged as a risk factor in patients showcasing mild liver fibrosis.
期刊介绍:
Antiviral Research is a journal that focuses on various aspects of controlling viral infections in both humans and animals. It is a platform for publishing research reports, short communications, review articles, and commentaries. The journal covers a wide range of topics including antiviral drugs, antibodies, and host-response modifiers. These topics encompass their synthesis, in vitro and in vivo testing, as well as mechanisms of action. Additionally, the journal also publishes studies on the development of new or improved vaccines against viral infections in humans. It delves into assessing the safety of drugs and vaccines, tracking the evolution of drug or vaccine-resistant viruses, and developing effective countermeasures. Another area of interest includes the identification and validation of new drug targets. The journal further explores laboratory animal models of viral diseases, investigates the pathogenesis of viral diseases, and examines the mechanisms by which viruses avoid host immune responses.