Yuefeng Wang, etc.,al. Metabolomic Profiling of Plasma Reveals Differential Disease Severity Markers in avian influenza A(H7N9) infection Patients. International Journal of Infectious Diseases
Objectives
Avian influenza such as H7N9 is currently a major global public health risk, and at present, there is a lack of relevant diagnostic and treatment markers.
Methods
We collected plasma samples from 104 confirmed H7N9 patients, 31 of whom died. Plasma metabolites were detected by UHPLC-HRMS, and a survival prediction model based on metabolites was constructed by machine learning models.
Results
A total of 1536 metabolites were identified in the plasma samples of H7N9 patients, of which 64 metabolites were up-regulated and 35 metabolites were down-regulated in the death group. The enrichment analysis of Tryptophan metabolism, Porphyrin metabolism and Riboflavin metabolism were significantly up-regulated in the death group. We found that most Lipids and lipid?like molecules were down-regulated in the death group, and Organoheterocyclic compounds were significantly up-regulated in the death group. A machine learning model was constructed for predicting mortality based on Porphobilinogen, 5-Hydroxyindole-3-acetic acid, L-Kynurenine, Biliverdin, and D-Dimer. The AUC on the test set was 0.929.
Conclusions
We first revealed the plasma metabolomic characteristics of H7N9 patients and found that a machine learning model based on plasma metabolites could predict the risk of death for H7N9 in the early stage of admission.
Avian influenza such as H7N9 is currently a major global public health risk, and at present, there is a lack of relevant diagnostic and treatment markers.
Methods
We collected plasma samples from 104 confirmed H7N9 patients, 31 of whom died. Plasma metabolites were detected by UHPLC-HRMS, and a survival prediction model based on metabolites was constructed by machine learning models.
Results
A total of 1536 metabolites were identified in the plasma samples of H7N9 patients, of which 64 metabolites were up-regulated and 35 metabolites were down-regulated in the death group. The enrichment analysis of Tryptophan metabolism, Porphyrin metabolism and Riboflavin metabolism were significantly up-regulated in the death group. We found that most Lipids and lipid?like molecules were down-regulated in the death group, and Organoheterocyclic compounds were significantly up-regulated in the death group. A machine learning model was constructed for predicting mortality based on Porphobilinogen, 5-Hydroxyindole-3-acetic acid, L-Kynurenine, Biliverdin, and D-Dimer. The AUC on the test set was 0.929.
Conclusions
We first revealed the plasma metabolomic characteristics of H7N9 patients and found that a machine learning model based on plasma metabolites could predict the risk of death for H7N9 in the early stage of admission.
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