代谢组学
接收机工作特性
萧条(经济学)
药品
代谢组
肠道菌群
钥匙(锁)
毒品天真
代谢物
高香草酸
生物
重性抑郁障碍
药物代谢
计算生物学
曲线下面积
曲线下面积
医学
代谢网络
药理学
药物发现
心理学
调解
双歧杆菌
微生物群
粪便
神经科学
生物信息学
作者
Mingliang Zhao,Penghong Liu,Mingzhi Pan,Yuhuai Guo,Tao Sun,Zhenxing Ren,Xiaojiao Zheng,Mengci Li,Xiaowen Chao,Jijun Wang,Jiahui Zeng,Xiaohua Liu,Yong Yang,Peiyang Luo,Dan Zheng,Junliang Kuang,Keke Ding,Aihua Zhao,Kun Ge,Yingjun Ouyang
标识
DOI:10.1016/j.xcrm.2025.102574
摘要
Mounting evidence highlights the interplay between gut microbiota, metabolism, and depression. In this study, we analyze fecal and serum metabolomes in first-episode depression and matched controls (n = 186), with validation in three independent cohorts (n = 223, 85, 52) including drug intervention. Significant disruptions are noted in 53 gut microbial species, 12 microbiota-related metabolic pathways, and 34 metabolites in depressive individuals compared to controls. Sixteen metabolites exhibit reversal after drug administration. Partial Spearman analysis identifies 271 species-metabolite correlations, and mediation analysis unveils 61 metabolite-mediated species-depression correlations. Key features associated with depression, including Bifidobacterium longum, Parasutterella excrementihominis, tyrosine, serotonin, and homovanillic acid, are highlighted. A machine learning model with 34 metabolites achieves area under the receiver operating characteristic (ROC) curve values of 0.82 and 0.80 in discriminating depression from control in test and validation sets. Our findings highlight metabolites as key mediators linking microbiota to depression and as valuable indicators for its identification.
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