Long-term clinical outcomes in steatotic liver disease and incidence of liver-related events, cardiovascular events and all-cause mortality

被引:13
|
作者
Tamaki, Nobuharu [1 ,2 ]
Kimura, Takefumi [3 ]
Wakabayashi, Shun-Ichi [3 ]
Umemura, Takeji [3 ]
Kurosaki, Masayuki [1 ]
Loomba, Rohit [2 ]
Izumi, Namiki [1 ]
机构
[1] Musashino Red Cross Hosp, Dept Gastroenterol & Hepatol, 1-26-1 Kyonan Cho, Musashino, Tokyo 180861, Japan
[2] Univ Calif San Diego, MASLD Res Ctr, Dept Med, Div Gastroenterol & Hepatol, La Jolla, CA USA
[3] Shinshu Univ, Dept Med, Div Gastroenterol, Sch Med, Nagano, Japan
关键词
ALCOHOL-CONSUMPTION; RISK; METAANALYSIS; IMPACT;
D O I
10.1111/apt.18015
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: A multi-society consensus group proposed a new nomenclature for steatotic liver disease (SLD) including metabolic-dysfunction associated steatotic liver disease (MASLD), MASLD and increased alcohol intake (MetALD) and alcohol-associated liver disease (ALD). However, the risk of liver-related events, major adverse cardiovascular events (MACE) and all-cause mortality among various sub-groups is unknown. Aims: To evaluate the risk of liver-related events, MACE and death among patients with SLD. Methods: We conducted a nationwide, population-based study and enrolled 761,400 patients diagnosed with MASLD, MetALD or ALD. The primary endpoint was the occurrence of liver-related events, MACE and death in patients with MASLD, MetALD and ALD. Results: The cumulative incidence of liver-related events and death were highest in ALD, followed by MetALD and MASLD (p < 0.001 for both liver-related events and death), while the incidence of MACE was highest in MASLD, followed by MetALD and ALD (p < 0.001). Using MASLD as the reference and adjusting for age, sex, smoking, diabetes mellitus, dyslipidaemia and hypertension, the adjusted hazard ratios (95% confidence intervals) for liver-related events, MACE and death in MetALD were 1.42 (1.1-1.8), 0.68 (0.63-0.73) and 1.13 (0.98-1.3), respectively. In ALD, they were 3.42 (2.6-4.6), 0.58 (0.49-0.67) and 1.60 (1.3-2.0), respectively, for liver-related events, MACE and death. Conclusions: The new consensus nomenclature can be used to stratify the risk of complications and prognosis. The nomenclature is beneficial for risk stratification and identifying new mechanisms for disease-specific therapeutic implications.
引用
收藏
页码:61 / 69
页数:9
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