Steatotic liver disease predicts cardiovascular disease and advanced liver fibrosis: A community-dwelling cohort study with 20-year follow-up

被引:36
作者
Choe, Hun Jee [1 ]
Moon, Joon Ho [2 ,3 ]
Kim, Won [2 ,4 ]
Koo, Bo Kyung [2 ,4 ]
Cho, Nam H. [5 ,6 ]
机构
[1] Hallym Univ, Dongtan Sacred Heart Hosp, Dept Internal Med, Hwaseong, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul, South Korea
[3] Seoul Natl Univ, Bundang Hosp, Dept Internal Med, Seongnam, South Korea
[4] Seoul Metropolitan Govt Boramae Med Ctr, Dept Internal Med, Seoul, South Korea
[5] Ajou Univ, Sch Med, Dept Prevent Med, Suwon, South Korea
[6] Ajou Univ, Dept Prevent Med & Publ Hlth, Sch Med, 64 World Cup Ro, Suwon, Gyeonggi Do, South Korea
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 2024年 / 153卷
基金
新加坡国家研究基金会;
关键词
Alcohol-associated liver disease (ALD); Advanced fibrosis; Cardiovascular disease; Metabolic dysfunction-associated steatotic liver; disease; MASLD with increased alcohol intake; (MetALD); Steatotic liver disease; DIAGNOSIS; OBESITY; RISK;
D O I
10.1016/j.metabol.2024.155800
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Steatotic liver disease (SLD) has emerged as new nomenclature to increase awareness and reflect the pathophysiology of the disease better. We investigated the risk of advanced fibrosis and cardiovascular disease (CVD) in SLD using data derived from a Korean prospective cohort. Methods: We defined SLD using the fatty liver index (FLI) and identified advanced fibrosis with the age-adjusted Fibrosis-4 Index. SLD was further subcategorized into metabolic dysfunction-associated SLD (MASLD), MASLD with increased alcohol intake (MetALD), and alcohol-associated liver disease (ALD). Findings: The Ansung-Ansan cohort of the Korean Genome and Epidemiology study, following 9497 participants from 2002 to 2020, included 3642 (38.3%) with MASLD, 424 (4.5%) with MetALD, and 207 (2.1%) with ALD. During the median follow-up of 17.5 years, CVD risk was higher in those with MASLD (hazard ratio [HR], 1.27; 95% confidence interval [CI], 1.12-1.45; P < 0.001), MetALD (HR, 1.88; 95% CI, 1.33-2.65; P < 0.001), and ALD (HR, 1.95; 95% CI, 1.01-3.77; P < 0.001) than in those without SLD, after adjusting for conventional risk factors. Notably, CVD risk was higher in the MetALD than in the MASLD group (P = 0.027). In the MASLD group, the number of cardiometabolic risk factors (CMRFs) correlated positively with CVD risk (HR, 1.34; 95% CI, 1.24-1.45; P < 0.001 for trend). Among the CMRFs, hypertension (HR, 1.94; 95% CI, 1.63-2.31; P < 0.001) was the predominant contributor to CVD. The MASLD (HR, 1.39; 95% CI, 1.25-1.55; P < 0.001), MetALD (HR, 1.75; 95% CI, 1.38-2.23; P < 0.001), and ALD (HR, 2.00; 95% CI, 1.30-3.07; P = 0.002) groups had a higher risk of advanced fibrosis than did the non-SLD group (P < 0.001 for trend). Interpretation: Our study provides new insight into hepatic and cardiovascular outcomes related to SLD subtypes. The risk of CVD increased in the order of no SLD, MASLD, and MetALD. The SLD subcategories, considering CMRFs and alcohol intake, outperformed traditional fatty liver categorizations in predicting CVD risk. The proposed SLD terminology could impact clinical practice, warranting further exploration of the heterogeneity of clinical outcomes among SLD subtypes.
引用
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页数:9
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