Metabolomic profiling of dengue infection: unraveling molecular signatures by LC-MS/MS and machine learning models.

IF 3.5 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Jhansi Venkata Nagamani Josyula, Aashika Raagavi JeanPierre, Sachin B Jorvekar, Deepthi Adla, Vignesh Mariappan, Sai Sharanya Pulimamidi, Siva Ranganathan Green, Agieshkumar Balakrishna Pillai, Roshan M Borkar, Srinivasa Rao Mutheneni
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引用次数: 0

Abstract

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.

Methods: 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.

登革热感染的代谢组学分析:利用 LC-MS/MS 和机器学习模型揭示分子特征。
背景与目的:登革热发展为重症登革热(SD)是一个重大的公共卫生问题,损害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与机器模型相结合,以确定与非严重登革热患者和健康对照组相比,严重登革热患者体内表达不同的代谢物:全面收集登革热无预警征兆期(DWOW,N = 10)、登革热有预警征兆期(DWW,N = 10)和SD(N = 10)患者在不同临床阶段[即入院日(DOA)、休养日(DOD)和康复日(DOC)]与健康对照组(HC)的血浆。样本经 LC-ESI-MS/MS 鉴定代谢物。使用 R 和 Python 语言进行统计和机器学习分析。此外,还进行了生物标志物、路径和相关性分析,以确定登革热的潜在预测因子:所有研究组共鉴定出 423 种代谢物。配对和非配对 t 检验显示,登革热组之间和登革热组之间有 14 种高度差异表达的代谢物,其中四种代谢物(莽草酸、脲二酸、丙酰肉碱和α-生育酚)与登革热组相比有显著差异。此外,生物标志物(ROC)分析显示,11 个潜在分子的 AUC 值显著为 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的结局。逻辑回归模型显示,S-腺苷高半胱氨酸、低牛磺酸和莽草酸代谢物可作为预测重症登革热的有利指标,准确率和AUC值均为0.75。数据显示,登革热感染与脂质代谢、氧化应激、炎症、代谢组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衍生小分子生物标志物,并对与疾病严重程度相关的代谢组学机制提出了新的见解。
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来源期刊
Metabolomics
Metabolomics 医学-内分泌学与代谢
CiteScore
6.60
自引率
2.80%
发文量
84
审稿时长
2 months
期刊介绍: Metabolomics publishes current research regarding the development of technology platforms for metabolomics. This includes, but is not limited to: metabolomic applications within man, including pre-clinical and clinical pharmacometabolomics for precision medicine metabolic profiling and fingerprinting metabolite target analysis metabolomic applications within animals, plants and microbes transcriptomics and proteomics in systems biology Metabolomics is an indispensable platform for researchers using new post-genomics approaches, to discover networks and interactions between metabolites, pharmaceuticals, SNPs, proteins and more. Its articles go beyond the genome and metabolome, by including original clinical study material together with big data from new emerging technologies.
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