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Multi-omics dissection of MASLD reveals divergent pathways to systemic diseases and targets for prevention

delete2026-08-11
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PRE
AI
Y
Yuxuan Weng
M
Mingyi Du
T
Tianhao Wu
L
Linyao Lu
蒋艳峰 (Yanfeng Jiang)
索晨 (Chen Suo)
李金 cover
李金 (Jin Li)
T
Tiejun Zhang *
陈兴栋 (Xingdong Chen) *
刘振球 (Zhenqiu Liu) *
DOI:10.1016/j.metabol.2026.156734delete
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Abstract

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.

Journal

M
Metabolism-Clinical and Experimental
IF:
11.9
Papers:
9.6K
Citations:
2.1W

Organization

F
fudan university
Scholars:
11.3W
Papers: 7.6W
Citations: 121
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