Yu Simiao, Wang Sici, Li Ping, Zheng Haocheng, Jing Jing, He Tingting, Ding Xia, Wang Ruilin
Department of Hepatology of Traditional Chinese Medicine, The Fifth Medical Center of PLA General Hospital, Beijing, China.
Beijing University of Chinese Medicine, Beijing, China.
J Clin Transl Hepatol. 2025 Aug 28;13(8):619-629. doi: 10.14218/JCTH.2025.00073. Epub 2025 Jun 30.
Drug-induced liver injury (DILI) represents a prevalent adverse event associated with medication use. However, the exact mechanisms underlying DILI remain incompletely understood, and the lack of specific diagnostic and prognostic biomarkers poses significant challenges to the clinical diagnosis and treatment of this condition. Consequently, our study aimed to endeavor to identify serum and fecal metabolic biomarkers, enabling more accurate DILI diagnosis and improved prediction of chronic progression.
Untargeted metabolomics analysis was performed on serum and fecal samples obtained from a cohort of 32 DILI patients (causality confirmed via the updated Roussel Uclaf Causality Assessment Method) and 36 healthy controls. Utilizing techniques such as partial least squares-discriminant analysis modeling and t-tests, we identified significantly differentially expressed metabolites and metabolite sets. Causality assessment was performed using the updated Roussel Uclaf Causality Assessment Method.
The findings from the analysis of serum and fecal metabolomics association pathways suggested that perturbations in bile acid metabolism might serve as potential mechanisms underlying the progression of DILI. Our study revealed 22 overlapping differential metabolites between serum and feces, displaying significant concentration differences between the DILI and healthy control groups. Notably, we identified chenodeoxycholic acid and deoxycholic acid as promising markers that not only distinguished DILI patients from healthy individuals but also exhibited predictive potential for DILI chronicity.
The integrated analysis of serum and fecal metabolites uncovers the significant disruption of bile acid metabolites as a key contributing factor in the pathogenesis of DILI. Our study offers promising potential biomarkers for the diagnosis and prognosis of DILI, paving the way for a novel perspective in the realm of DILI diagnosis and treatment.
药物性肝损伤(DILI)是一种与药物使用相关的常见不良事件。然而,DILI的确切机制仍未完全明确,且缺乏特异性诊断和预后生物标志物给该疾病的临床诊断和治疗带来了重大挑战。因此,我们的研究旨在努力识别血清和粪便代谢生物标志物,以实现更准确的DILI诊断并改善对慢性进展的预测。
对32例DILI患者(通过更新的乌普萨拉监测中心因果关系评估方法确认因果关系)和36例健康对照者的血清和粪便样本进行非靶向代谢组学分析。利用偏最小二乘判别分析建模和t检验等技术,我们识别出显著差异表达的代谢物和代谢物集。使用更新的乌普萨拉监测中心因果关系评估方法进行因果关系评估。
血清和粪便代谢组学关联途径分析结果表明,胆汁酸代谢紊乱可能是DILI进展的潜在机制。我们的研究发现血清和粪便中有22种重叠的差异代谢物,在DILI组和健康对照组之间显示出显著的浓度差异。值得注意的是,我们将鹅去氧胆酸和脱氧胆酸确定为有前景的标志物,它们不仅能区分DILI患者和健康个体,还对DILI的慢性化具有预测潜力。
血清和粪便代谢物的综合分析揭示了胆汁酸代谢物的显著破坏是DILI发病机制中的一个关键因素。我们的研究为DILI的诊断和预后提供了有前景的潜在生物标志物,为DILI诊断和治疗领域开辟了新视角。