Zeng Guyu, Wang Peizhi, Xu Weiwei, Li Qinxue, Li Tianyu, Tian Yue, Huang Bochuan, Grobbee Diederick, Cabezas Manuel Castro, Yuan Jinqing
National Clinical Research Center for Cardiovascular Diseases, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Department of Cardiology, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Eur J Prev Cardiol. 2025 Jun 12. doi: 10.1093/eurjpc/zwaf330.
BACKGROUND & AIMS: Steatotic liver disease (SLD) is an overarching term to encompass metabolic-dysfunction associated steatotic liver disease (MASLD), MASLD with increased alcohol intake (MetALD), and alcohol-associated liver disease (ALD). However, the impact of metabolic syndrome (MetS) on the association between SLD and mortality risk remains uncertain. This study aims to compare all-cause and cause-specific mortality across SLD subtypes stratified by MetS.
A population-based cohort study was conducted using NHANES Ⅲ data, including 9,217 participants stratified by MetS status and further categorized into no SLD, MASLD, MetALD, and ALD groups. MetS was defined according to the International Diabetes Federation criteria.
Over a median follow-up of 26.4 years, 3,521 mortality events occurred. After adjustment, SLD with MetS was significantly associated with an increased risk of all-cause mortality compared with healthy controls (HR 1.56, 95% CI 1.38-1.75). This association persisted across all SLD subtypes (MASLD: HR 1.52, 95% CI 1.34-1.72; MetALD: HR 1.92, 95% CI 1.41-2.62; ALD: HR 2.80, 95% CI 1.56-5.05). In contrast, no significant association was found between SLD subtypes without MetS and mortality risk. When stratified by MetS presence, MASLD, MetALD and ALD were each significantly associated with increased mortality risks compared to the no SLD group in individuals with MetS, primarily driven by high cancer-related and diabetes-related mortality. However, this association was not observed in the population without MetS.
This study reveals that the significant association between SLD subtypes and mortality risk is mediated by MetS. To enhance risk stratification and improve long-term health outcomes, it is crucial to distinguish between MASLD, MetALD, and other SLD types while managing metabolic status and reducing alcohol consumption.
脂肪性肝病(SLD)是一个综合术语,涵盖代谢功能障碍相关脂肪性肝病(MASLD)、酒精摄入量增加的MASLD(MetALD)和酒精性肝病(ALD)。然而,代谢综合征(MetS)对SLD与死亡风险之间关联的影响仍不确定。本研究旨在比较按MetS分层的SLD各亚型的全因死亡率和特定病因死亡率。
使用美国国家健康与营养检查调查(NHANES)Ⅲ数据进行了一项基于人群的队列研究,包括9217名参与者,按MetS状态分层,并进一步分为无SLD、MASLD、MetALD和ALD组。MetS根据国际糖尿病联盟标准定义。
在中位随访26.4年期间,发生了3521例死亡事件。调整后,与健康对照相比,伴有MetS的SLD与全因死亡风险增加显著相关(风险比[HR]1.56,95%置信区间[CI]1.38 - 1.75)。这种关联在所有SLD亚型中均持续存在(MASLD:HR 1.52,95% CI 1.34 - 1.72;MetALD:HR 1.92,95% CI 1.41 - 2.62;ALD:HR 2.80,95% CI 1.56 - 5.05)。相比之下,无MetS的SLD亚型与死亡风险之间未发现显著关联。按是否存在MetS分层时,与无SLD组相比,在伴有MetS的个体中,MASLD、MetALD和ALD各自与死亡风险增加显著相关,主要由高癌症相关死亡率和糖尿病相关死亡率驱动。然而,在无MetS的人群中未观察到这种关联。
本研究表明,SLD亚型与死亡风险之间的显著关联是由MetS介导的。为了加强风险分层并改善长期健康结局,在管理代谢状态和减少酒精消费时,区分MASLD、MetALD和其他SLD类型至关重要。