全代谢组关联确定铁氧化还原蛋白-1 (FDX1)是亚洲人群胆固醇代谢和心血管风险的决定因素。

IF 9.4 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Nature cardiovascular research Pub Date : 2025-05-01 Epub Date: 2025-05-13 DOI:10.1038/s44161-025-00638-w
Nilanjana Sadhu, Rinkoo Dalan, Pritesh R Jain, Chang Jie Mick Lee, Leroy Sivappiragasam Pakkiri, Kai Yi Tay, Theresia H Mina, Dorrain Low, Yilin Min, Matthew Ackers-Johnson, Thi Tun Thi, Vishnu Goutham Kota, Yu Shi, Yan Liu, Hanry Yu, Vicky Lai, Yang Yang, Darwin Tay, Hong Kiat Ng, Xiaoyan Wang, Kari E Wong, Max Lam, Xue Li Guan, Nicolas Bertin, Eleanor Wong, James Best, Rangaprasad Sarangarajan, Paul Elliott, Elio Riboli, Jimmy Lee, Eng Sing Lee, Joanne Ngeow, Patrick Tan, Christine Cheung, Chester Lee Drum, Roger Sy Foo, Gregory A Michelotti, Haojie Yu, Patricia A Sheridan, Marie Loh, John C Chambers
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引用次数: 0

摘要

与欧洲和北美心血管疾病死亡率下降形成对比的是,亚太区域的心血管疾病负担正在上升。在这里,我们对8124名亚洲成年人进行了883种代谢物的非靶向质谱定量分析,并研究了它们与颈动脉内膜中膜厚度(动脉粥样硬化的标志)的关系。胆固醇代谢物3β -羟基-5-胆固醇酸酯(3BH5C)的血浆浓度与颈动脉内膜中膜厚度呈负相关,孟德尔随机化研究支持3BH5C与冠状动脉疾病之间的因果关系。观察到的效应量在亚洲人身上是欧洲人的5到6倍。共定位分析表明,3BH5C血浆水平与铁氧化还原蛋白1 (FDX1)的信使RNA和蛋白表达之间存在共同的因果变异,铁氧化还原蛋白1是固醇和胆汁酸合成所必需的蛋白质。我们通过敲除和过表达模型验证了FDX1是肝细胞和巨噬细胞中3BH5C合成的调节因子,并证明了其在巨噬细胞和主动脉平滑肌细胞中胆固醇外排中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metabolome-wide association identifies ferredoxin-1 (FDX1) as a determinant of cholesterol metabolism and cardiovascular risk in Asian populations.

The burden of cardiovascular disease is rising in the Asia-Pacific region, in contrast to falling cardiovascular disease mortality rates in Europe and North America. Here we perform quantification of 883 metabolites by untargeted mass spectroscopy in 8,124 Asian adults and investigate their relationships with carotid intima media thickness, a marker of atherosclerosis. Plasma concentrations of 3beta-hydroxy-5-cholestenoate (3BH5C), a cholesterol metabolite, were inversely associated with carotid intima media thickness, and Mendelian randomization studies supported a causal relationship between 3BH5C and coronary artery disease. The observed effect size was 5- to 6-fold higher in Asians than Europeans. Colocalization analyses indicated the presence of a shared causal variant between 3BH5C plasma levels and messenger RNA and protein expression of ferredoxin-1 (FDX1), a protein that is essential for sterol and bile acid synthesis. We validated FDX1 as a regulator of 3BH5C synthesis in hepatocytes and macrophages and demonstrated its role in cholesterol efflux in macrophages and aortic smooth muscle cells, using knockout and overexpression models.

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CiteScore
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