Dynamic FIB-4 Score Changes and HCC Risk in Patients with MASLD and Elevated Liver Enzymes: A Nationwide Cohort Study.

IF 10.5 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Liver Cancer Pub Date : 2026-01-12 DOI:10.1159/000550360
Yee Hui Yeo, Hsiu J Ho, Tsai-Wei Huang, Teng-Yu Lee, Ju Dong Yang, George Cholankeril, Chien-Jen Chen, Hawi-I Yang, Chuen-Fei Chen, Hung-Chuen Chang, Chun-Ying Wu
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引用次数: 0

Abstract

Introduction: Hepatocellular carcinoma (HCC) can develop in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD) without cirrhosis, especially in those with elevated liver enzymes. However, there is currently no low-cost, scalable screening tool for this population. To address this need, we investigated the association between serial changes in FIB-4 (fibrosis-4) scores over a 3-year period and the risk of developing HCC in a large, diverse cohort of patients with MASLD without cirrhosis.

Methods: This study utilized a nationwide cohort from the National Health Insurance Research Database (NHIRD), including 810,698 patients with MASLD who had demographic and laboratory data at baseline and at least 3 years of follow-up. FIB-4 scores were analyzed to assess transitions between low-risk (<1.45), indeterminate-risk (1.45-2.67), and high-risk (>2.67) categories over time. Competing risks for HCC and mortality were modeled to estimate the sub-distribution hazard ratios (SHRs).

Results: Changes in FIB-4 scores over time provided superior predictive accuracy compared to one-time measurement. Individuals with persistent high FIB-4 (high-to-high group) had a 14-fold higher risk of developing HCC (adjusted SHR [aSHR] 13.91, 95% CI: 11.94-16.20) compared to those with stably low FIB-4 (low-to-low group), while those with improved scores (high-to-low and high-to-indeterminate groups) had a lower risk compared to the high-to-high group. Worsening FIB-4 scores, as shown in the low-to-indeterminate group (aSHR 2.22, 95% CI: 1.93-2.57 or the low-to-high group (aSHR 4.75, 95% CI: 3.38-6.68), were associated with progressively increased risks of HCC compared to the low-to-low group. In contrast, when compared to the high-to-high group, those with improved FIB-4 scores, including the high-to-indeterminate group (aSHR 0.41, 95% CI: 0.35-0.48) and the high-to-low group (aSHR 0.25, 95% CI: 0.15-0.42), exhibited reduced HCC risks.

Conclusion: Serial FIB-4 measurements offer greater accuracy in identifying individuals at high risk for HCC in non-cirrhotic MASLD Asians with elevated liver enzymes, with HCC surveillance warranted in high-risk groups.

MASLD和肝酶升高患者的动态FIB-4评分变化和HCC风险:一项全国性队列研究
肝细胞癌(HCC)可在无肝硬化的代谢功能障碍相关脂肪变性肝病(MASLD)患者中发展,特别是在肝酶升高的患者中。然而,目前还没有针对这一人群的低成本、可扩展的筛查工具。为了满足这一需求,我们在一个大型、多样化的无肝硬化MASLD患者队列中调查了3年期间FIB-4(纤维化-4)评分的系列变化与发生HCC风险之间的关系。方法:本研究利用来自国家健康保险研究数据库(NHIRD)的全国队列,包括810,698例MASLD患者,他们在基线和至少3年的随访时具有人口统计学和实验室数据。分析FIB-4评分以评估低风险(2.67)类别之间随时间的转变。对HCC和死亡率的竞争风险进行建模,以估计亚分布风险比(SHRs)。结果:与一次性测量相比,FIB-4评分随时间的变化提供了更高的预测准确性。与稳定的低FIB-4(低到低组)相比,持续高FIB-4(高到高组)的个体发生HCC的风险高14倍(调整后的SHR [aSHR] 13.91, 95% CI: 11.94-16.20),而得分提高的个体(高到低和高到不确定组)的风险比高到高组低。与低至低组相比,低至不确定组(aSHR 2.22, 95% CI: 1.93-2.57)或低至高组(aSHR 4.75, 95% CI: 3.38-6.68)的FIB-4评分恶化与HCC风险逐渐增加相关。相比之下,与高到高组相比,FIB-4评分提高的患者,包括高到不确定组(aSHR 0.41, 95% CI: 0.35-0.48)和高到低组(aSHR 0.25, 95% CI: 0.15-0.42), HCC风险降低。结论:在肝酶升高的非肝硬化MASLD亚洲患者中,连续FIB-4测量可更准确地识别HCC高危人群,对高危人群进行HCC监测是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Liver Cancer
Liver Cancer Medicine-Oncology
CiteScore
20.80
自引率
7.20%
发文量
53
审稿时长
16 weeks
期刊介绍: Liver Cancer is a journal that serves the international community of researchers and clinicians by providing a platform for research results related to the causes, mechanisms, and therapy of liver cancer. It focuses on molecular carcinogenesis, prevention, surveillance, diagnosis, and treatment, including molecular targeted therapy. The journal publishes clinical and translational research in the field of liver cancer in both humans and experimental models. It publishes original and review articles and has an Impact Factor of 13.8. The journal is indexed and abstracted in various platforms including PubMed, PubMed Central, Web of Science, Science Citation Index, Science Citation Index Expanded, Google Scholar, DOAJ, Chemical Abstracts Service, Scopus, Embase, Pathway Studio, and WorldCat.
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