Roulot Dominique, Layese Richard, Brichler Ségolène, Ganne Nathalie, Asselah Tarik, Zoulim Fabien, Gordien Emmanuel, Nahon Pierre, Roudot-Thoraval Françoise
AP-HP, Hôpital Avicenne, Unité d'Hépatologie, Bobigny; Université Sorbonne Paris Nord, F-93000 Bobigny; Inserm U955, équipe 18, Université Paris-Est, Créteil, France.
Université Paris-Est Créteil, INSERM, IMRB, CEpiA (Clinical Epidemiology and Ageing Unit) Team, Créteil; AP-HP, Hôpital Henri-Mondor, Unité de Recherche Clinique (URC Mondor), F-94010 Créteil, France.
Clin Gastroenterol Hepatol. 2024 Oct 24. doi: 10.1016/j.cgh.2024.08.046.
BACKGROUND & AIMS: The specific causative role of hepatitis delta virus (HDV) infection in the development of hepatocellular carcinoma (HCC) remains debated and was not specifically demonstrated in patients with cirrhosis. Here we compared HCC incidence in hepatitis B virus (HBV)-HDV coinfected and HBV monoinfected patients with cirrhosis.
A total of 142 HBV-HDV and 271 HBV-infected patients with cirrhosis from the French ANRSCO12 CirVir and DeltaVir cohorts, with histologically proven cirrhosis and no history of decompensation, were included in the study.
HBV-HDV patients were younger than HBV patients (37.2 vs 53.8 years), they were more often immigrants from sub-Saharan Africa, and displayed less comorbidities and more altered liver tests. After adjustment for age, cumulative incidences of HCC in coinfected and monoinfected patients at 1, 3, and 5 years were 5.2%, 11.8%, and 20.2% versus 1.1%, 2.5%, and 4.4%, respectively (P < .001). In multivariate analysis, HDV infection was an independent factor associated with the development of HCC (hazard ratio [HR], 2.94; 95% confidence interval [CI], 1.19-7.25; P = .019). Other independent factors were age (HR, 1.08; 95% CI, 1.05-1.11; P < .001), overweight (HR, 0.45; 95% CI, 0.22-0.93; P = .031), smoking (HR, 2.26; 95% CI, 1.23-4.16; P = .009), increased γ-glutamyltransferase (HR, 2.73; 95% CI, 1.24-6.00; P = .013), total bilirubin >17 μmol/L (HR, 2.68; 95% CI, 1.33-5.42; P = .006), and platelet count <150.000/mm (HR, 3.11; 95% CI, 1.51-6.41; P = .002). HDV coinfection was not an independent factor of liver decompensation, transplantation, or death.
The incidence of HCC seems significantly higher in HBV-HDV than in HBV-infected patients with cirrhosis. HDV infection emerges as an independent risk factor for HCC, indicating that in patients with cirrhosis, HDV plays a causative role for HCC independently of HBV.
丁型肝炎病毒(HDV)感染在肝细胞癌(HCC)发生中的具体致病作用仍存在争议,且在肝硬化患者中未得到明确证实。在此,我们比较了乙型肝炎病毒(HBV)-HDV合并感染和HBV单感染的肝硬化患者中HCC的发病率。
本研究纳入了来自法国ANRS CO12 CirVir和DeltaVir队列的142例HBV-HDV合并感染和271例HBV感染的肝硬化患者,这些患者经组织学证实为肝硬化且无失代偿病史。
HBV-HDV患者比HBV患者年轻(37.2岁对53.8岁),他们更多是来自撒哈拉以南非洲的移民,合并症较少,肝功能检查异常更多。在调整年龄后,合并感染和单感染患者在1年、3年和5年时HCC的累积发病率分别为5.2%、11.8%和20.2%,而单感染患者分别为1.1%、2.5%和4.4%(P <.001)。在多变量分析中,HDV感染是与HCC发生相关的独立因素(风险比[HR],2.94;95%置信区间[CI],1.19 - 7.25;P =.019)。其他独立因素包括年龄(HR,1.08;95% CI,1.05 - 1.11;P <.001)、超重(HR,0.45;95% CI,0.22 - 0.93;P =.031)、吸烟(HR,2.26;95% CI,1.23 - 4.16;P =.009)、γ-谷氨酰转移酶升高(HR,2.73;95% CI,1.24 - 6.00;P =.013)、总胆红素>17 μmol/L(HR,2.68;95% CI,1.33 - 5.42;P =.006)以及血小板计数<150,000/mm³(HR,3.11;95% CI,1.51 - 6.41;P =.002)。HDV合并感染不是肝失代偿、移植或死亡的独立因素。
HBV-HDV合并感染患者中HCC的发病率似乎显著高于HBV感染的肝硬化患者。HDV感染是HCC的独立危险因素,表明在肝硬化患者中,HDV独立于HBV对HCC起致病作用。