Two-step clinical care pathway to predict MASLD-related advanced fibrosis and long-term outcomes in type 2 diabetes

瞬态弹性成像 医学 内科学 失代偿 肝活检 队列 2型糖尿病 前瞻性队列研究 肝纤维化 2型糖尿病 糖尿病 队列研究 肝病 胃肠病学 糖化血红素 脂肪肝 脂肪变性 活检 丙型肝炎 外科 肝病学 纤维化 试验预测值 回顾性队列研究 非酒精性脂肪肝 代谢综合征
作者
Yuping Chen,Bingtian Dong,Xinrui Jin,Chuan Liu,Ming‐Hua Zheng,Xiao Liang,Yameng Sun,Hye Won Lee,Huapeng Lin,Emmanuel A. Tsochatzis,Salvatore Petta,Elisabetta Bugianesi,Masato Yoneda,Hannes Hagström,Jérôme Boursier,Calleja Jl,George Boon‐Bee Goh,W K Chan,Rocío Gallego‐Durán,Arun Jayant Sanyal
出处
期刊:Gut [BMJ]
卷期号:75 (3): 576-587 被引量:9
标识
DOI:10.1136/gutjnl-2025-337506
摘要

BACKGROUND: Current guidelines recommend a two-step approach for risk stratification of metabolic dysfunction-associated steatotic liver disease (MASLD), starting with Fibrosis-4 index (FIB-4) followed by liver stiffness measurement (LSM) using vibration-controlled transient elastography (VCTE). OBJECTIVE: To evaluate this approach for predicting advanced fibrosis and liver-related events (LREs) in patients with type 2 diabetes (T2D). DESIGN: A prospective liver biopsy cohort of T2D patients with histologically confirmed MASLD from seven centres in China was used to assess diagnostic performance for advanced fibrosis. The international VCTE-Prognosis cohort, including T2D patients with MASLD who underwent VCTE at 16 centres in the USA, Europe and Asia, with longitudinal follow-up, was used to assess LREs, defined as hepatic decompensation or hepatocellular carcinoma. RESULTS: 4781 participants were included. In the liver biopsy cohort (n=352; 22.2% with advanced fibrosis), applying LSM thresholds of <8 kPa and >12 kPa after FIB-4 classified patients into 63.4% low-risk, 9.4% intermediate-risk and 27.3% high-risk, with a correct classification rate of 71%. In the VCTE-Prognosis cohort (n=4429; median follow-up 51.3 (IQR 27.4-70.7) months), 140 (3.2%) patients developed LREs (110 (2.5%) with hepatic decompensation and 59 (1.3%) with hepatocellular carcinoma). The two-step approach classified 72.6%, 6.8% and 20.6% of patients into low-risk, intermediate-risk and high-risk groups, with corresponding 5-year cumulative LRE incidences of 0.7%, 0.9% and 11.8%. Refining classification of intermediate FIB-4 patients using LSM <10 kPa (low-risk) and >15 kPa (high-risk) reduced the intermediate-risk group to 5.6% while preserving predictive accuracy. CONCLUSION: The non-invasive two-step approach of FIB-4 followed by LSM effectively stratifies MASLD-related advanced fibrosis and LREs risk in T2D. Applying LSM cut-offs of 10 and 15 kPa further optimises risk stratification for future LREs.
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