Department of Gastroenterology & Hepatology, Erasmus Medical Center, Rotterdam, The Netherlands.
Francis Family Liver Clinic, Toronto Centre for Liver Disease, Toronto, Ontario, Canada.
BMJ Open Gastroenterol. 2023 Dec 7;10(1):e001209. doi: 10.1136/bmjgast-2023-001209.
Historical paired liver biopsy studies are likely to underestimate current progression of disease in patients with chronic hepatitis C virus (HCV) infection. We aimed to assess liver disease progression according to the non-invasive Fibrosis-4 (FIB-4) index in patients with chronic HCV and early disease.
Patients diagnosed with chronic HCV and FIB-4 <3.25 from four international liver clinics were included in a retrospective cohort study. Follow-up ended at start of antiviral therapy resulting in sustained virological response, at time of liver transplantation or death. Primary outcome of advanced liver disease was defined as FIB-4 >3.25 during follow-up. Survival analyses were used to assess time to FIB-4 >3.25.In total, 4286 patients were followed for a median of 5.0 (IQR 1.7-9.4) years, during which 41 071 FIB-4 measurements were collected. At baseline, median age was 47 (IQR 39-55) years, 2529 (59.0%) were male, and 2787 (65.0%) patients had a FIB-4 <1.45. Advanced liver disease developed in 821 patients. Overall, 10-year cumulative incidence of advanced disease was 32.1% (95% CI 29.9% to 34.3%). Patients who developed advanced disease showed an exponential FIB-4 increase. Among patients with a presumed date of HCV infection, cumulative incidence of advanced disease increased 7.7-fold from 20 to 40 years as opposed to the first 20 years after HCV infection.
The rate of advanced liver disease is high among chronic HCV-infected patients with early disease at time of diagnosis, among whom liver disease progression accelerated over time. These results emphasise the need to overcome any limitations with respect to diagnosing and treating all patients with chronic HCV across the globe.
历史上的配对肝活检研究可能低估了慢性丙型肝炎病毒 (HCV) 感染患者当前疾病的进展。我们旨在评估慢性 HCV 和早期疾病患者根据无创性 Fibrosis-4 (FIB-4) 指数的肝病进展情况。
从四个国际肝脏诊所诊断为慢性 HCV 和 FIB-4<3.25 的患者被纳入回顾性队列研究。随访在开始抗病毒治疗导致持续病毒学应答、肝移植或死亡时结束。晚期肝病的主要结局定义为随访期间 FIB-4>3.25。生存分析用于评估达到 FIB-4>3.25 的时间。共对 4286 例患者进行了中位数为 5.0(IQR 1.7-9.4)年的随访,在此期间共收集了 41071 次 FIB-4 测量值。基线时,中位年龄为 47(IQR 39-55)岁,2529 例(59.0%)为男性,2787 例(65.0%)患者的 FIB-4<1.45。821 例患者出现晚期肝病。总体而言,10 年累积发生率为 32.1%(95%CI 29.9%至 34.3%)。出现晚期疾病的患者 FIB-4 呈指数增加。在假定 HCV 感染日期的患者中,与 HCV 感染后前 20 年相比,40 年时的晚期疾病累积发生率增加了 7.7 倍。
在诊断时患有早期疾病的慢性 HCV 感染患者中,晚期肝病的发生率较高,且随着时间的推移,肝病进展加速。这些结果强调了需要克服全球范围内诊断和治疗所有慢性 HCV 患者的任何限制。