生命银行
大脑结构与功能
神经影像学
蛋白质组
神经科学
孟德尔随机化
脑图谱
大脑大小
生物
计算生物学
生物信息学
医学
基因
遗传学
磁共振成像
放射科
基因型
遗传变异
作者
Peng Ren,Xiao‐He Hou,Zeyu Li,Jia You,Yuzhu Li,Wei Zhang,Weikang Gong,Bei Zhang,Bang‐Sheng Wu,Linbo Wang,Chun Shen,Yujie Zhao,Qing Ma,Jujiao Kang,Yuchao Jiang,Neil Roberts,Fan Xu,Yong He,Jin‐Tai Yu,Meiyun Wang
标识
DOI:10.1038/s41467-025-60185-7
摘要
Individual variation in brain structure influences deterioration due to disease and comprehensive profiling of the associated proteomic signature advances mechanistic understanding. Here, using data from 4997 UK Biobank participants, we analyzed the associations between 2920 plasma proteins and 272 neuroimaging-derived brain structure measures. We identified 5358 associations between 1143 proteins and 256 brain structure measures, with NCAN and LEP proteins showing the most associations. Functional enrichment implicated these proteins in neurogenesis, immune/apoptotic processes and neurons. Furthermore, bidirectional Mendelian randomization revealed 33 associations between 32 proteins and 23 brain structure measures, and 21 associations between nine brain structure associated proteins and ten brain disorders. Moreover, the significant associations between the identified proteins and mental health were mediated by brain volume and surface area. In summary, this study generates a comprehensive atlas mapping the patterns of association between proteome and brain structure, highlighting their potential value for studying brain disorders.
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