代谢综合征
蛋白质组学
人口
医学
分类器(UML)
内科学
生物信息学
计算生物学
生物
计算机科学
环境卫生
人工智能
肥胖
遗传学
基因
作者
Xue Cai,Zhangzhi Xue,Fangfang Zeng,Jun Tang,Liang Yue,Bo Wang,Weigang Ge,Yuting Xie,Zelei Miao,Wanglong Gou,Yuanqing Fu,Sainan Li,Jinlong Gao,Menglei Shuai,Ke Zhang,Fengzhe Xu,Yunyi Tian,Nan Xiang,Yan Zhou,Peng‐Fei Shan
标识
DOI:10.1016/j.xcrm.2023.101172
摘要
Metabolic syndrome (MetS) is a complex metabolic disorder with a global prevalence of 20%–25%. Early identification and intervention would help minimize the global burden on healthcare systems. Here, we measured over 400 proteins from ∼20,000 proteomes using data-independent acquisition mass spectrometry for 7,890 serum samples from a longitudinal cohort of 3,840 participants with two follow-up time points over 10 years. We then built a machine-learning model for predicting the risk of developing MetS within 10 years. Our model, composed of 11 proteins and the age of the individuals, achieved an area under the curve of 0.774 in the validation cohort (n = 242). Using linear mixed models, we found that apolipoproteins, immune-related proteins, and coagulation-related proteins best correlated with MetS development. This population-scale proteomics study broadens our understanding of MetS and may guide the development of prevention and targeted therapies for MetS.
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