Section of Gastroenterology and Hepatology, Department of Medicine, Baylor College of Medicine, Houston, Texas, USA; Hepatology Program, Division of Abdominal Transplantation, Michael E DeBakey Department of General Surgery, Baylor College of Medicine, Houston, Texas, USA.
Section of Health Services Research, Department of Medicine, Baylor College of Medicine, Houston, Texas, USA; Center for Innovations in Quality, Effectiveness and Safety, Michael E. DeBakey Veterans Affairs Medical Center, Houston, Texas, USA.
J Hepatol. 2023 Mar;78(3):493-500. doi: 10.1016/j.jhep.2022.10.035. Epub 2022 Nov 17.
BACKGROUND & AIMS: Currently, there is no consistent information on the course of fibrosis-4 (FIB-4) score changes in non-alcoholic fatty liver disease (NAFLD) or their association with subsequent risk of cirrhosis and/or hepatocellular carcinoma (HCC). Thus, we aimed to evaluate the association between longitudinal changes in FIB-4 and subsequent risk of HCC and a composite endpoint of cirrhosis and HCC in patients with NAFLD.
We conducted a retrospective cohort study of patients with NAFLD seen in 130 Veterans Administration hospitals between 1/1/2004-12/31/2008, with follow-up through to 12/31/2018. We calculated FIB-4 longitudinally and categorized patients based on risk of advanced fibrosis (low-risk FIB-4 <1.45, indeterminate-risk FIB-4 1.45-2.67, and high-risk FIB-4 >2.67). We used landmark Fine-Gray competing risks models to determine the effects of change in FIB-4 between NAFLD diagnosis date and 3-year landmark time on the subsequent risk of HCC and a composite endpoint.
Among the 202,319 patients with NAFLD in the 3-year landmark analysis, 473 progressed to HCC at an incidence rate of 0.28 per 1,000 person years (PY) (95% CI 0.26-0.30). The incidence rate of the composite endpoint was 1.31 per 1,000 PY (95% CI 1.25-1.37). At baseline, 74.7%, 21.4%, and 3.8% of patients had a low, indeterminate, and high FIB-4, respectively. Compared to patients who were at stable low FIB-4 at both time points, the risk of HCC and that of the composite endpoint was higher for all other subgroups with the highest risk in patients with persistently high FIB-4 (HCC adjusted sub-distribution hazard ratio 57.7, 95% CI 40.5-82.2 and composite endpoint hazard ratio 28.6, 95% CI 24.6-33.2).
Longitudinal changes in FIB-4 were strongly associated with progression to cirrhosis and HCC.
Tools to stratify the risk of HCC development in patients with NAFLD are currently lacking. The fibrosis-4 (FIB-4) score is a widely available non-invasive test for liver fibrosis, a primary determinant of the development of cirrhosis and HCC. In a large retrospective cohort of patients with NAFLD, we found that serial changes in FIB-4 over time were strongly associated with progression to cirrhosis and HCC. Integrating serial measurements of non-invasive tests for fibrosis into the care pathway for patients with NAFLD could help tailor HCC risk prevention.
目前,非酒精性脂肪性肝病(NAFLD)患者肝纤维化 4 指数(FIB-4)评分变化的过程及其与肝硬化和/或肝细胞癌(HCC)发生风险的关系尚无一致信息。因此,我们旨在评估 NAFLD 患者 FIB-4 纵向变化与 HCC 及肝硬化和 HCC 复合终点的发生风险之间的关系。
我们对 2004 年 1 月 1 日至 2008 年 12 月 31 日期间在 130 家退伍军人事务部医院就诊的 NAFLD 患者进行了回顾性队列研究,随访至 2018 年 12 月 31 日。我们对 FIB-4 进行了纵向计算,并根据晚期纤维化风险(低风险 FIB-4<1.45、不确定风险 FIB-4 1.45-2.67 和高风险 FIB-4>2.67)对患者进行了分类。我们使用 landmark Fine-Gray 竞争风险模型来确定在 NAFLD 诊断日期和 3 年 landmark 时间之间 FIB-4 变化对 HCC 及肝硬化和 HCC 复合终点的后续风险的影响。
在 3 年 landmark 分析中,202319 例 NAFLD 患者中有 473 例发生 HCC,发病率为 0.28/1000 人年(95%CI 0.26-0.30)。复合终点的发病率为 1.31/1000 人年(95%CI 1.25-1.37)。基线时,74.7%、21.4%和 3.8%的患者分别具有低、不确定和高 FIB-4。与两个时间点 FIB-4 稳定低值的患者相比,所有其他亚组的 HCC 和复合终点风险更高,持续高 FIB-4 患者的风险最高(HCC 调整后的亚分布风险比为 57.7,95%CI 40.5-82.2,复合终点风险比为 28.6,95%CI 24.6-33.2)。
FIB-4 的纵向变化与肝硬化和 HCC 的进展密切相关。
目前缺乏用于分层 NAFLD 患者 HCC 发生风险的工具。肝纤维化 4 指数(FIB-4)评分是一种广泛应用的非侵入性肝纤维化检测方法,是肝硬化和 HCC 发生的主要决定因素。在一项针对大量 NAFLD 患者的回顾性队列研究中,我们发现 FIB-4 随时间的连续变化与肝硬化和 HCC 的进展密切相关。将纤维化的非侵入性检测的连续测量值整合到 NAFLD 患者的护理途径中,可能有助于针对 HCC 风险进行个体化预防。