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Multi-omics dissection of MASLD reveals divergent pathways to systemic diseases and targets for prevention
Y
M
T
L
蒋
索
T
陈
刘
DOI:10.1016/j.metabol.2026.156734.png)
Abstract
En 中文
• MASLD comprises three genetic subtypes with distinct biological roots. • All subtypes increase liver disease risk but diverge in cardiometabolic outcomes. • Plasma protein signatures distinguish each subtype and link them to systemic disease. • Both established and potentially novel protein targets emerged as candidates for personalized prevention.
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