医学
肝纤维化
内科学
胃肠病学
纤维化
阶段(地层学)
病理
肝病
人肝
风险评估
作者
Xiaodong Zhou,Qin‐Fen Chen,Qi Fan,Seung Up Kim,Terry Cheuk‐Fung Yip,Salvatore Petta,Atsushi Nakajima,Emmanuel Tsochatzis,Jérôme Boursier,Elisabetta Bugianesi,Hannes Hagström,Wah‐Kheong Chan,Manuel Romero‐Gómez,José Luís Calleja,Victor de Lédinghen,Laurent Castéra,Arun J. Sanyal,George Boon‐Bee Goh,Philip N. Newsome,Jian-Gao Fan
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2025-12-16
被引量:10
标识
DOI:10.1097/hep.0000000000001645
摘要
BACKGROUND: Cardiovascular-kidney-metabolic (CKM) syndrome, a new framework integrating cardiovascular, renal, and metabolic dysfunction, remains inadequately characterized in metabolic dysfunction-associated steatotic liver disease (MASLD). OBJECTIVE: We investigated the relationships between CKM stages and liver fibrosis severity, progression, and the risk of liver-related events (LREs) in MASLD. DESIGN: Patients with MASLD from the VCTE-Prognosis cohort were stratified according to CKM stages. Outcomes included the prevalence of advanced liver fibrosis (LSM ≥10 kPa), liver stiffness progression (≥20% increase and Baveno category upshift), and incident LREs. Associations were assessed using multivariable logistic regression and Cox proportional hazards models. RESULTS: Among 12,097 patients with MASLD, the prevalence of advanced liver fibrosis increased across CKM stages at baseline: 9.6% (CKM stage 0-1), 18.0% (CKM stage 2), and 31.6% (CKM stage 3-4). CKM stage 2 (adjusted OR=1.663, 95% CI 1.444-1.915) and CKM stage 3-4 (adjusted OR=2.575, 95% CI 2.109-3.144) were independently associated with advanced fibrosis. During a 4.5-year median follow-up, 716 patients (6.1%) experienced progression of liver stiffness, and 352 patients (1.7%) developed LRE. Compared with CKM stage 0-1, the risk of liver stiffness progression was higher in CKM stage 2 (adjusted HR=1.321, 95% CI 1.050-1.662; p =0.018) and CKM stage 3-4 (adjusted HR=1.767, 95% CI 1.339-2.330; p <0.001). In contrast, only CKM stage 3-4 were significantly associated with an increased risk of LREs (adjusted HR=1.975, 95% CI 1.245-3.133; p =0.004). CONCLUSIONS: CKM stages are independently associated with the severity and progression of liver fibrosis in MASLD. CKM stage 2 significantly increases liver stiffness progression without excess LRE risk, while CKM stage 3-4 confer the highest risk for liver-related outcomes.
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