脂肪肝指数动态作为2型糖尿病和非肝硬化患者肝细胞癌的预测因子。

Eun-Hee Cho, Min Gu Kang, Chang Hun Lee, Shinyoung Oh, Chen Shen, Ha Ram Oh, Young Ran Park, Hyun Lee, Jong Seung Kim, Ji Hyun Park
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引用次数: 0

摘要

背景:2型糖尿病(T2DM)是非酒精性脂肪性肝病患者发生肝细胞癌(HCC)的重要危险因素;然而,对T2DM患者,特别是无肝硬化患者的监测策略是不充分的。本研究探讨了脂肪肝指数(FLI)及其动态变化是否能有效识别T2DM HCC风险增高患者。方法:对2012年至2015年接受两次健康筛查的92761例40 - 79岁T2DM患者的数据进行分析。FLI由腰围、体重指数、甘油三酯和γ -谷氨酰转移酶计算,通过基线FLI和筛查之间的FLI变化对患者进行分层。通过国际疾病分类代码和报销记录(2016年至2020年)确定HCC病例。结果:基线FLI为30 ~ 59.9的患者发生HCC的风险增加1.90倍(p)。结论:基线和动态监测FLI可有效识别非肝硬化T2DM患者的HCC风险,支持早期发现和干预。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fatty Liver Index Dynamics as a Predictor of Hepatocellular Carcinoma in Patients with Type 2 Diabetes Mellitus and Non-Cirrhotic Livers.

Background: Type 2 diabetes mellitus (T2DM) is a significant risk factor for hepatocellular carcinoma (HCC) in patients with nonalcoholic fatty liver disease; however, surveillance strategies for patients with T2DM, especially without cirrhosis, are inadequate. This study examined whether the fatty liver index (FLI) and its dynamic changes can effectively identify patients with T2DM at increased risk for HCC.

Methods: Data from 92,761 individuals with T2DM aged 40 to 79 who underwent two health screenings (2012 to 2015) were analyzed. The FLI, calculated using waist circumference, body mass index, triglycerides, and gamma-glutamyl transferase, was used to stratify patients by baseline FLI and FLI changes between screenings. HCC cases were identified via International Classification of Diseases codes and reimbursement records (2016 to 2020).

Results: Patients with baseline FLI of 30 to 59.9 had a 1.90-fold higher risk (P<0.01) and those with FLI ≥60 had a 2.94-fold higher risk (P<0.01) of developing HCC compared to those with FLI <30. An increase in FLI from <30 to ≥30 resulted in a 2.10-fold higher risk of HCC (P<0.01), while a reduction in FLI from ≥30 to <30 led to a 0.64-fold lower risk (P=0.03). Protective benefits of FLI reduction took approximately 3 years to manifest.

Conclusion: Baseline and dynamic monitoring of FLI effectively identified HCC risk in T2DM patients with non-cirrhotic livers, supporting early detection and intervention.

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