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纤维化标志物的纵向变化与非酒精性脂肪性肝病患者发生肝硬化和肝细胞癌的风险相关。

Longitudinal changes in fibrosis markers are associated with risk of cirrhosis and hepatocellular carcinoma in non-alcoholic fatty liver disease.

机构信息

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.

出版信息

J Hepatol. 2023 Mar;78(3):493-500. doi: 10.1016/j.jhep.2022.10.035. Epub 2022 Nov 17.

Abstract

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.

METHODS

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.

RESULTS

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).

CONCLUSION

Longitudinal changes in FIB-4 were strongly associated with progression to cirrhosis and HCC.

IMPACT AND IMPLICATIONS

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.

摘要

背景与目的

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。

方法

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。

结果

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)。

结论

FIB-4 的纵向变化与肝硬化和 HCC 的进展密切相关。

影响与意义

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。

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