Department of Applied Biology, CSIR-Indian Institute of Chemical Technology, Tarnaka, Hyderabad, Telangana, 500007, India.
Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India.
Metabolomics. 2024 Sep 21;20(5):104. doi: 10.1007/s11306-024-02169-0.
BACKGROUND & OBJECTIVE: The progression of dengue fever to severe dengue (SD) is a major public health concern that impairs the capacity of the medical system to predict and treat dengue patients. Hence, the present study used a metabolomic approach integrated with machine models to identify differentially expressed metabolites in patients with SD compared to nonsevere patients and healthy controls.
Comprehensively, the plasma was collected at different clinical phases during dengue without warning signs (DWOW, N = 10), dengue with warning signs (DWW, N = 10), and SD (N = 10) at different stages [i.e., day of admission (DOA), day of defervescence (DOD), and day of convalescent (DOC)] in comparison to healthy control (HC). The samples were subjected to LC‒ESI‒MS/MS to identify metabolites. Statistical and machine learning analyses were performed using R and Python language. Further, biomarker, pathway and correlation analysis was performed to identify potential predictors of dengue.
RESULTS & CONCLUSION: A total of 423 metabolites were identified in all the study groups. Paired and unpaired t-tests revealed 14 highly differentially expressed metabolites between and across the dengue groups, with four metabolites (shikimic acid, ureidosuccinic acid, propionyl carnitine, and alpha-tocopherol) showing significant differences compared to HC. Furthermore, biomarker (ROC) analysis revealed 11 potential molecules with a significant AUC value of 1 that could serve as potential biomarkers for identifying different dengue clinical stages that are beneficial for predicting dengue disease outcomes. The logistic regression model revealed that S-adenosylhomocysteine, hypotaurine, and shikimic acid metabolites could be beneficial indicators for predicting severe dengue, with an accuracy and AUC of 0.75. The data showed that dengue infection is related to lipid metabolism, oxidative stress, inflammation, metabolomic adaptation, and virus manipulation. Moreover, the biomarkers had a significant correlation with biochemical parameters like platelet count, and hematocrit. These results shed some light on host-derived small-molecule biomarkers that are associated with dengue severity and novel insights into metabolomics mechanisms interlinked with disease severity.
登革热进展为重症登革热(SD)是一个重大的公共卫生问题,它削弱了医疗系统预测和治疗登革热患者的能力。因此,本研究采用代谢组学方法结合机器模型,鉴定 SD 患者与非重症患者和健康对照组之间差异表达的代谢物。
全面收集无预警症状登革热(DWOW,N=10)、有预警症状登革热(DWW,N=10)和 SD(N=10)患者在不同临床阶段的血浆样本,以及健康对照组(HC)。对样本进行 LC-ESI-MS/MS 以鉴定代谢物。使用 R 和 Python 语言进行统计和机器学习分析。进一步进行生物标志物、途径和相关性分析,以确定登革热的潜在预测因子。
在所有研究组中总共鉴定出 423 种代谢物。配对和非配对 t 检验显示 14 种代谢物在登革热组之间存在高度差异表达,其中 4 种代谢物(莽草酸、尿刊酸、丙酰肉碱和α-生育酚)与 HC 相比具有显著差异。此外,生物标志物(ROC)分析显示 11 种潜在分子具有显著的 AUC 值 1,可作为识别不同登革热临床阶段的潜在生物标志物,有利于预测登革热疾病结局。逻辑回归模型显示,S-腺苷同型半胱氨酸、牛磺酸和莽草酸代谢物可能是预测重症登革热的有益指标,准确率和 AUC 为 0.75。数据表明,登革热感染与脂质代谢、氧化应激、炎症、代谢组学适应和病毒操纵有关。此外,这些生物标志物与血小板计数和血细胞比容等生化参数有显著相关性。这些结果揭示了与登革热严重程度相关的宿主来源小分子生物标志物,并为疾病严重程度相关的代谢组学机制提供了新的见解。