医学
危险系数
狼牙棒
内科学
比例危险模型
脂肪肝
肝病
脂肪变性
疾病
置信区间
心肌梗塞
传统PCI
作者
Daniel Clayton‐Chubb,Ammar Majeed,Isabella Commins,Robyn L. Woods,Andrew T. Chan,Joanne Ryan,Franz‐Josef Neumann,Hans G. Schneider,Andrew Tonkin,Mark Nelson,Sharyn M. Fitzgerald,Suzanne G. Orchard,John Lubel,Daniel Sikavi,Cammie Tran,Alexander Hodge,John J. McNeil,William Kemp,Stuart K. Roberts
标识
DOI:10.1097/hc9.0000000000000756
摘要
Background: Steatotic liver disease (SLD) is a significant cause of chronic liver disease. However, the relative prevalence and prognostic significance of various disease entities according to recently defined classification systems (MAFLD vs. the SLD-spectrum of MASLD, Met-ALD, and ALD) is understudied in older adults. Methods: Post hoc analysis of the ASPirin in Reducing Events in the Elderly (ASPREE) study involving 16,703 Australian community-dwelling adults aged ≥70 years free from significant disability, prior cardiovascular disease events, and with a life expectancy ≥5 years. Steatosis was identified by Fatty Liver Index (FLI) ≥60. Alcohol intake was self-reported. SLD subtypes were classified according to European Association for the Study of the Liver (EASL)/American Association for the Study of Liver Diseases (AASLD) guidelines. Cox regression was used to estimate hazard ratios for adjudicated outcomes: mortality, major adverse cardiovascular events (MACE), and persistent physical disability. Results: Of 9847 participants with calculable FLI and a median 8.6 years follow-up, 3748 (38.1%) had hepatic steatosis. Substratifying by MAFLD criteria versus the SLD type, 3743 had MAFLD (38.0%), and 3464 (35.2%) met SLD criteria (MASLD 3132 [90.4%], Met-ALD 262 [7.6%], ALD 74 [2.0%]) (excluding steatogenic medication users). There was no increased mortality risk with MAFLD or SLD. MAFLD and MASLD were associated with MACE when adjusted for age and sex (HR 1.42 [95% CI 1.17–1.71] and HR 1.40 [95% CI 1.15–1.71], respectively), but not in the fully adjusted model. MAFLD, MASLD, and ALD were associated with an increased risk of persistent physical disability even when fully adjusted (HR 1.46 [95% CI 1.19–1.79], HR 1.49 [95% CI 1.20–1.83], HR 2.53 [95% CI 1.27–5.05], respectively), but not Met-ALD. Conclusions: MAFLD and the metabolic-SLD spectrum are common in community-dwelling older adults. No subclassification is associated with increased mortality in this group, although there is an association between both MACE and persistent physical disability with SLD.
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