Metabolomics and machine learning approaches for diagnostic and prognostic biomarkers screening in sepsis

被引:5
|
作者
She, Han [1 ,2 ]
Du, Yuanlin [1 ,2 ]
Du, Yunxia [1 ,2 ]
Tan, Lei [1 ,2 ]
Yang, Shunxin [1 ,2 ]
Luo, Xi [1 ,2 ]
Li, Qinghui [2 ]
Xiang, Xinming [2 ]
Lu, Haibin [3 ]
Hu, Yi [1 ]
Liu, Liangming [2 ]
Li, Tao [2 ]
机构
[1] Army Med Univ, Daping Hosp, Dept Anesthesiol, Chongqing 400042, Peoples R China
[2] Army Med Univ, Daping Hosp, Shock & Transfus Dept, State Key Lab Trauma Burns & Combined Injury, Chongqing 400042, Peoples R China
[3] Army Med Univ, Daping Hosp, Dept Intens Care Unit, Chongqing 400042, Peoples R China
关键词
Sepsis; Metabolomics; Biomarker; Machine learning; Phenylalanine metabolism; DISCRIMINATION;
D O I
10.1186/s12871-023-02317-4
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
BackgroundSepsis is a life-threatening disease with a poor prognosis, and metabolic disorders play a crucial role in its development. This study aims to identify key metabolites that may be associated with the accurate diagnosis and prognosis of sepsis.MethodsSeptic patients and healthy individuals were enrolled to investigate metabolic changes using non-targeted liquid chromatography-high-resolution mass spectrometry metabolomics. Machine learning algorithms were subsequently employed to identify key differentially expressed metabolites (DEMs). Prognostic-related DEMs were then identified using univariate and multivariate Cox regression analyses. The septic rat model was established to verify the effect of phenylalanine metabolism-related gene MAOA on survival and mean arterial pressure after sepsis.ResultsA total of 532 DEMs were identified between healthy control and septic patients using metabolomics. The main pathways affected by these DEMs were amino acid biosynthesis, phenylalanine metabolism, tyrosine metabolism, glycine, serine and threonine metabolism, and arginine and proline metabolism. To identify sepsis diagnosis-related biomarkers, support vector machine (SVM) and random forest (RF) algorithms were employed, leading to the identification of four biomarkers. Additionally, analysis of transcriptome data from sepsis patients in the GEO database revealed a significant up-regulation of the phenylalanine metabolism-related gene MAOA in sepsis. Further investigation showed that inhibition of MAOA using the inhibitor RS-8359 reduced phenylalanine levels and improved mean arterial pressure and survival rate in septic rats. Finally, using univariate and multivariate cox regression analysis, six DEMs were identified as prognostic markers for sepsis.ConclusionsThis study employed metabolomics and machine learning algorithms to identify differential metabolites that are associated with the diagnosis and prognosis of sepsis patients. Unraveling the relationship between metabolic characteristics and sepsis provides new insights into the underlying biological mechanisms, which could potentially assist in the diagnosis and treatment of sepsis.Trial registrationThis human study was approved by the Ethics Committee of the Research Institute of Surgery (2021-179) and was registered by the Chinese Clinical Trial Registry (Date: 09/12/2021, ChiCTR2200055772).
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页数:13
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