孟德尔随机化
代谢组学
代谢综合征
疾病
医学
因果关系(物理学)
代谢组
脂肪肝
生物信息学
非酒精性脂肪肝
生命银行
糖尿病
动脉粥样硬化性心血管疾病
代谢途径
肝病
生理学
不利影响
生物
情感(语言学)
肥胖
内科学
脂蛋白
老年学
脂肪变性
随机对照试验
生物标志物
内分泌学
脂质代谢
作者
Rongtao Jiang,Matthew Rosenblatt,Shile Qi,Vince D. Calhoun,Qian Wang,Peng Wang,J I A H U I Wu,Dustin Scheinost,Jing Sui
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2026-05-13
卷期号:12 (20): eaeg4939-eaeg4939
标识
DOI:10.1126/sciadv.aeg4939
摘要
Prevention remains a key strategy to address the growing burden of metabolic dysfunction-associated steatotic liver disease (MASLD), highlighting the importance of exploring modifiable risk factors. Accumulating evidence suggests a close link between physical frailty and MASLD. However, how frailty interacts with metabolic syndrome to affect MASLD and the causality and direction of the association remain largely unknown. Leveraging data from 405,224 UK Biobank participants with a 13.65-year follow-up, we found that physical frailty was associated with an increased risk of clinically diagnosed MASLD and exacerbated the adverse effect of metabolic syndrome on MASLD incidence, implying that frail people may be more vulnerable to this disease because of metabolic syndrome. Mendelian randomization provided evidence for a potential causal effect of physical frailty on MASLD but not the reverse direction. Moreover, the metabolome-wide association analysis revealed widespread associations of plasma metabolites with both frailty and MASLD, suggesting a shared metabolomic foundation between them. Some metabolites, including fatty acids and triglyceride-rich lipoprotein biomarkers, partially explained the frailty-MASLD relationship, indicating a potential metabolomic mechanism. If confirmed in further studies, frailty screening may help identify high-risk individuals and inform early prevention for MASLD, especially for those with metabolic syndrome.
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