Clayton-Chubb Daniel, Roberts Stuart K, Majeed Ammar, Woods Robyn L, Tonkin Andrew M, Nelson Mark R, Chan Andrew T, Ryan Joanne, Tran Cammie, Hodge Alexander, Lubel John S, Schneider Hans G, Brodtmann Amy, Fitzgerald Sharyn M, Orchard Suzanne G, McNeil John J, Kemp William W
Department of Gastroenterology, The Alfred Hospital Health, 99 Commercial Road, Melbourne, VIC, 3004, Australia.
Department of Medicine, School of Translational Medicine, Monash University, Melbourne, Australia.
Geroscience. 2025 Feb;47(1):1303-1318. doi: 10.1007/s11357-024-01435-2. Epub 2024 Nov 28.
The impact of metabolic dysfunction-associated steatotic liver disease (MASLD), the preferred nomenclature for NAFLD, on cardiovascular health and mortality among older adults is uncertain. As such, we aimed to identify whether MASLD increases the risk of Major Adverse Cardiovascular Events (MACE) (a composite of fatal coronary heart disease [excluding heart failure], nonfatal myocardial infarction, or fatal or nonfatal ischemic stroke), Atrial Fibrillation (AF), or all-cause mortality in older adults, and whether aspirin attenuates these risks in individuals with MASLD. This is a non-prespecified post-hoc analysis of the ASPREE (ASPirin in Reducing Events in the Elderly) randomized trial. Participants were community dwelling well adults aged ≥ 70 years without a history of atherosclerotic cardiovascular disease or AF. Fatty Liver Index (FLI) was used to identify MASLD at baseline. FLI is a composite of anthropometric and biochemical markers used in epidemiologic studies to rule in and rule out hepatic steatosis. MACE and cause of death were adjudicated by clinical experts; AF was assessed by previously defined algorithm in ASPREE. 9,097 participants were stratified into groups according to FLI. In univariate analysis, prevalent MASLD (FLI ≥ 60 with evidence of metabolic dysfunction; n = 2,998 [33.0%]) was associated with an increased risk of MACE (HR 1.47 [95% CI 1.22-1.78]) and AF (HR 1.50 [95% CI 1.19-1.88] but not all-cause mortality (HR 1.04 [95% CI 0.91-1.19]). After adjusting for cardiovascular disease risk factors, only the association between MASLD and AF remained significant (HR 1.46 [95% CI 1.11-1.93]). Aspirin did not reduce the risk of MACE, death, or AF in the MASLD group. MASLD was associated with an increased hazard of incident AF, but not of MACE or all-cause mortality, in community dwelling older adults. Primary prevention with aspirin does not ameliorate these risks in older adults with MASLD.
代谢功能障碍相关脂肪性肝病(MASLD),即非酒精性脂肪性肝病(NAFLD)的首选命名法,对老年人心血管健康和死亡率的影响尚不确定。因此,我们旨在确定MASLD是否会增加老年人发生主要不良心血管事件(MACE,包括致命性冠心病[不包括心力衰竭]、非致命性心肌梗死或致命或非致命性缺血性中风)、心房颤动(AF)或全因死亡的风险,以及阿司匹林是否能降低患有MASLD个体的这些风险。这是对ASPREE(老年人使用阿司匹林降低事件风险)随机试验进行的一项非预先指定的事后分析。参与者为年龄≥70岁、无动脉粥样硬化性心血管疾病或AF病史的社区居住健康成年人。在基线时使用脂肪肝指数(FLI)来识别MASLD。FLI是流行病学研究中用于判断和排除肝脂肪变性的人体测量和生化标志物的综合指标。MACE和死亡原因由临床专家判定;AF通过ASPREE中先前定义的算法进行评估。9097名参与者根据FLI分层。在单变量分析中, prevalent MASLD(FLI≥60且有代谢功能障碍证据;n = 2998 [33.0%])与MACE风险增加(HR 1.47 [95% CI 1.22 - 1.78])和AF风险增加(HR 1.50 [95% CI 1.19 - 1.88])相关,但与全因死亡无关(HR 1.04 [95% CI 0.91 - 1.19])。在调整心血管疾病风险因素后,只有MASLD与AF之间的关联仍然显著(HR 1.46 [95% CI 1.11 - 1.93])。阿司匹林并未降低MASLD组发生MACE、死亡或AF的风险。在社区居住的老年人中,MASLD与新发AF风险增加相关,但与MACE或全因死亡风险增加无关。对患有MASLD的老年人进行阿司匹林一级预防并不能改善这些风险。