Prediction of outcomes in patients with metabolic dysfunction-associated steatotic liver disease based on initial measurements and subsequent changes in magnetic resonance elastography

被引:7
作者
Kobayashi, Takashi [1 ]
Iwaki, Michihiro [1 ]
Nogami, Asako [1 ]
Kawamura, Nobuyoshi [1 ,2 ]
Honda, Yasushi [1 ]
Ogawa, Yuji [1 ,3 ]
Imajo, Kento [1 ,2 ]
Yoneda, Masato [1 ]
Saito, Satoru [1 ]
Nakajima, Atsushi [1 ]
机构
[1] Yokohama City Univ, Grad Sch Med, Dept Gastroenterol & Hepatol, 3-9 Fukuura,Kanazawa Ku, Yokohama 2360004, Japan
[2] Shin Yurigaoka Gen Hosp, Dept Gastroenterol, Kawasaki, Japan
[3] Natl Hosp Org Yokohama Med Ctr, Gastroenterol Div, Yokohama, Japan
关键词
Metabolic dysfunction-associated steatotic liver disease; Magnetic resonance elastography; Non-invasive test; Liver stiffness measurement; MR ELASTOGRAPHY; FIBROSIS STAGE; MORTALITY;
D O I
10.1007/s00535-023-02049-9
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: The prognosis of metabolic dysfunction-associated steatotic liver disease (MASLD) is strongly associated with liver fibrosis. We aimed to investigate whether liver stiffness measurement (LSM) and changes in LSM (Delta LSM) on magnetic resonance elastography (MRE) can predict clinical events in patients with MASLD. Methods: We included 405 patients with MASLD who underwent at least two MREs. The patients were divided into five groups corresponding to fibrosis stages (0-4) based on initial LSM and classified as progressors (Delta LSM >= 19%) or non-progressors (Delta LSM < 19%) based on the difference between the first and last LSM. Results: The mean follow-up period was 72.6 months, and the mean interval between MREs was 23.5 months. There were 52 (12.8%) progressors and 353 (87.2%) non-progressors. The initial LSM was significantly associated with the cumulative probabilities of decompensated cirrhosis, hepatocellular carcinoma (HCC), liver-related events, extrahepatic malignancies, and overall mortality but not with cardiovascular disease. Progressors had significantly higher hazard ratios (HRs) for decompensated cirrhosis, HCC, and liver-related events but not for extrahepatic malignancies, cardiovascular disease, or overall mortality. Among patients without cirrhosis, the HR for developing cirrhosis among progressors was 60.15. Progressors had a significantly higher risk of liver-related events, even in the low initial LSM (fibrosis stage 0-2) subgroups. Conclusions: Both initial LSM and Delta LSM can predict liver-related events in patients with MASLD, even for low initial LSM. This integrated assessment can allow more detailed risk stratification compared with single LSM assessments and identify high-risk patients with MASLD among those previously considered as low risk.
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页码:56 / 65
页数:10
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