Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.
Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
J Viral Hepat. 2021 Oct;28(10):1431-1442. doi: 10.1111/jvh.13577. Epub 2021 Jul 28.
Hepatitis D virus (HDV) infection causes a severe chronic viral hepatitis with accelerated development of liver cirrhosis and decompensation, but whether it further increases the risk of hepatocellular carcinoma (HCC) is unclear. We performed a comprehensive systematic review of the published literature and meta-analysis to assess the risk of HCC in HDV and hepatitis B virus (HBV) co-infected, compared to HBV mono-infected patients. The study was conducted per a priori defined protocol, including only longitudinal studies, thus excluding cross-sectional studies. Random-effects models were used to determine aggregate effect sizes (ES) with 95% confidence intervals (CI). Meta-regression was used to examine the associations among study level characteristics. Twelve cohort studies comprising a total of 6099 HBV/HDV co-infected and 57,620 chronic HBV mono-infected patients were analysed. The overall pooled ES showed that HBV/HDV co-infected patients were at 2-fold increased risk of HCC compared to HBV mono-infected patients (ES = 2.12, 95% CI 1.14-3.95, I = 72%, N = 12). A six-fold significant increased risk of HCC was noted among HIV/HBV/HDV triple-infected, compared to HIV/HBV co-infected patients. The magnitude of ES did not differ significantly after adjustment for study design and quality, publication year and follow-up duration in univariable meta-regression analysis. This systematic review and meta-analysis shows that infection with HDV is associated with a 2-fold higher risk of HCC development compared to HBV mono-infection. HCC surveillance strategies taking this increased risk into account, and new treatment options against HDV, are warranted.
丁型肝炎病毒 (HDV) 感染可导致严重的慢性病毒性肝炎,加速肝硬化和肝功能失代偿的发展,但它是否会进一步增加肝细胞癌 (HCC) 的风险尚不清楚。我们对已发表的文献进行了全面的系统评价和荟萃分析,以评估 HDV 和乙型肝炎病毒 (HBV) 合并感染患者与 HBV 单感染患者相比 HCC 的风险。该研究按照预先确定的方案进行,仅纳入了纵向研究,因此排除了横断面研究。采用随机效应模型确定汇总效应大小 (ES) 和 95%置信区间 (CI)。Meta 回归用于检查研究水平特征之间的关联。纳入了 12 项队列研究,共包括 6099 例 HBV/HDV 合并感染和 57620 例慢性 HBV 单感染患者。总体汇总 ES 表明,与 HBV 单感染患者相比,HBV/HDV 合并感染患者 HCC 的风险增加了 2 倍(ES=2.12,95%CI 1.14-3.95,I=72%,N=12)。与 HIV/HBV 合并感染患者相比,HIV/HBV/HDV 三重感染患者 HCC 的风险显著增加了 6 倍。在单变量 meta 回归分析中,调整研究设计和质量、发表年份和随访时间后,ES 的大小没有显著差异。本系统评价和荟萃分析表明,与 HBV 单感染相比,HDV 感染与 HCC 发展风险增加 2 倍相关。需要考虑到这种风险增加的 HCC 监测策略和针对 HDV 的新治疗选择。