Rahadini Adinda A D, Rahadina Adinda
Internal Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.
Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia.
Clin Exp Hepatol. 2025 Jun;11(2):129-136. doi: 10.5114/ceh.2025.151896. Epub 2025 Jun 13.
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.
We conducted a search of PubMed and Google Scholar from inception to July 7 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 .
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, < 0.00). No heterogeneity was present.
Metabolic dysfunction is associated with increased risk of HCC progression in CHC patients even after achieving SVR.
慢性丙型肝炎(CHC)感染仍然是全球最普遍的慢性肝病之一。接受直接抗病毒药物(DAA)治疗的CHC患者能够以较高比例实现持续病毒学应答(SVR)。然而,即使是实现SVR的小部分患者仍有发生肝细胞癌(HCC)的风险。代谢相关脂肪性肝病(MAFLD)与HCC风险增加相关。我们旨在总结MAFLD对CHC患者HCC发生的影响,即使是在实现SVR之后。
我们检索了PubMed和谷歌学术,检索时间从数据库建立至2024年7月7日,以查找评估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)的存在与实现SVR的CHC患者HCC风险之间关联的研究。使用纽卡斯尔-渥太华量表(NOS)评估纳入研究的质量。我们使用固定效应模型和随机效应模型分析了合并风险比(HR)及95%置信区间(CI)。使用 评估异质性。
纳入了五项研究,共7034例患者。研究质量为6至8星。代谢功能障碍与CHC患者SVR后HCC风险增加相关(HR = 2.02,95% CI:1.61 - 2.54,< 0.00)。不存在异质性问题。
即使在实现SVR后,代谢功能障碍仍与CHC患者HCC进展风险增加相关。