{"title":"HCV患者SVR后代谢性脂肪性肝病与HCC风险的相关性:一项系统回顾和荟萃分析","authors":"Adinda A D Rahadini, Adinda Rahadina","doi":"10.5114/ceh.2025.151896","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim of the study: </strong>Chronic hepatitis C (CHC) infection remains one of the most prevalent chronic liver disease worldwide. A sustained virological response (SVR) can be achieved at high rates for CHC patients receiving direct-acting antivirals (DAAs). However, even small subsets of patients achieving SVR still have a risk of developing hepatocellular carcinoma (HCC). Metabolic-associated fatty liver disease (MAFLD) is associated with increased risk of HCC. We aimed to summarize the effect of MAFLD on HCC development on CHC patients, even after achieving SVR.</p><p><strong>Material and methods: </strong>We conducted a search of PubMed and Google Scholar from inception to July 7<sup>th</sup> 2024, for studies assessing the association between the presence of MAFLD or metabolic dysfunction-associated steatotic liver disease (MASLD) or non-alcoholic fatty liver disease (NAFLD) and HCC risk in CHC patients who achieved SVR. The quality of included studies was evaluated using the Newcastle-Ottawa Scale (NOS). We analyzed the pooled hazard ratios (HRs) with 95% confidence intervals (CIs) using a fixed and random-effects model. Heterogeneity was assessed using <i>I</i> <sup>2</sup>.</p><p><strong>Results: </strong>Five studies with a total of 7,034 patients were included. The quality of studies ranged from 6 to 8 stars. Metabolic dysfunction is associated with increased risk of HCC after SVR in CHC patients (HR = 2.02, 95% CI: 1.61-2.54, <i>p</i> < 0.00). No heterogeneity was present.</p><p><strong>Conclusions: </strong>Metabolic dysfunction is associated with increased risk of HCC progression in CHC patients even after achieving SVR.</p>","PeriodicalId":10281,"journal":{"name":"Clinical and Experimental Hepatology","volume":"11 2","pages":"129-136"},"PeriodicalIF":1.7000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12403759/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association between metabolic associated fatty liver disease and HCC risk after SVR in HCV patients: A systematic review and meta-analysis.\",\"authors\":\"Adinda A D Rahadini, Adinda Rahadina\",\"doi\":\"10.5114/ceh.2025.151896\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aim of the study: </strong>Chronic hepatitis C (CHC) infection remains one of the most prevalent chronic liver disease worldwide. A sustained virological response (SVR) can be achieved at high rates for CHC patients receiving direct-acting antivirals (DAAs). However, even small subsets of patients achieving SVR still have a risk of developing hepatocellular carcinoma (HCC). Metabolic-associated fatty liver disease (MAFLD) is associated with increased risk of HCC. We aimed to summarize the effect of MAFLD on HCC development on CHC patients, even after achieving SVR.</p><p><strong>Material and methods: </strong>We conducted a search of PubMed and Google Scholar from inception to July 7<sup>th</sup> 2024, for studies assessing the association between the presence of MAFLD or metabolic dysfunction-associated steatotic liver disease (MASLD) or non-alcoholic fatty liver disease (NAFLD) and HCC risk in CHC patients who achieved SVR. The quality of included studies was evaluated using the Newcastle-Ottawa Scale (NOS). 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引用次数: 0
摘要
研究目的:慢性丙型肝炎(CHC)感染仍然是世界上最普遍的慢性肝病之一。对于接受直接作用抗病毒药物(DAAs)治疗的CHC患者,持续病毒学应答(SVR)的发生率很高。然而,即使一小部分达到SVR的患者仍有发生肝细胞癌(HCC)的风险。代谢性脂肪性肝病(MAFLD)与HCC风险增加相关。我们的目的是总结mald对CHC患者HCC发展的影响,即使在达到SVR之后。材料和方法:我们检索了PubMed和谷歌Scholar从成立到2024年7月7日的研究,以评估实现SVR的CHC患者中存在MAFLD或代谢功能障碍相关脂肪性肝病(MASLD)或非酒精性脂肪性肝病(NAFLD)与HCC风险之间的关系。采用纽卡斯尔-渥太华量表(NOS)评价纳入研究的质量。我们使用固定和随机效应模型分析95%置信区间(ci)的合并风险比(hr)。使用i2评估异质性。结果:纳入5项研究,共7034例患者。研究质量从6星到8星不等。CHC患者SVR后发生HCC的风险增加与代谢功能障碍相关(HR = 2.02, 95% CI: 1.61-2.54, p < 0.00)。不存在异质性。结论:代谢功能障碍与CHC患者HCC进展风险增加相关,即使在达到SVR后也是如此。
Association between metabolic associated fatty liver disease and HCC risk after SVR in HCV patients: A systematic review and meta-analysis.
Aim of the study: Chronic hepatitis C (CHC) infection remains one of the most prevalent chronic liver disease worldwide. A sustained virological response (SVR) can be achieved at high rates for CHC patients receiving direct-acting antivirals (DAAs). However, even small subsets of patients achieving SVR still have a risk of developing hepatocellular carcinoma (HCC). Metabolic-associated fatty liver disease (MAFLD) is associated with increased risk of HCC. We aimed to summarize the effect of MAFLD on HCC development on CHC patients, even after achieving SVR.
Material and methods: We conducted a search of PubMed and Google Scholar from inception to July 7th 2024, for studies assessing the association between the presence of MAFLD or metabolic dysfunction-associated steatotic liver disease (MASLD) or non-alcoholic fatty liver disease (NAFLD) and HCC risk in CHC patients who achieved SVR. The quality of included studies was evaluated using the Newcastle-Ottawa Scale (NOS). We analyzed the pooled hazard ratios (HRs) with 95% confidence intervals (CIs) using a fixed and random-effects model. Heterogeneity was assessed using I2.
Results: Five studies with a total of 7,034 patients were included. The quality of studies ranged from 6 to 8 stars. Metabolic dysfunction is associated with increased risk of HCC after SVR in CHC patients (HR = 2.02, 95% CI: 1.61-2.54, p < 0.00). No heterogeneity was present.
Conclusions: Metabolic dysfunction is associated with increased risk of HCC progression in CHC patients even after achieving SVR.
期刊介绍:
Clinical and Experimental Hepatology – quarterly of the Polish Association for Study of Liver – is a scientific and educational, peer-reviewed journal publishing original and review papers describing clinical and basic investigations in the field of hepatology.