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LC-MS/MS-Based Serum Metabolomics and Transcriptome Analyses for the Mechanism of Augmented Renal Clearance. | LitMetric

AI Article Synopsis

  • Augmented Renal Clearance (ARC) is characterized by increased renal solute clearance in critically ill patients, and a study utilized transcriptomics and metabolomics to explore its underlying causes.
  • Through transcriptomic analysis of 534 samples, 834 genes linked to ARC were identified, while metabolomic analysis revealed 45 key metabolites that were altered in patients with ARC.
  • The findings indicate significant changes in purine metabolism, arginine biosynthesis, and arachidonic acid metabolism, suggesting that inflammatory responses and various biochemical factors may influence renal blood flow and permeability in ARC patients.

Article Abstract

Augmented Renal Clearance (ARC) refers to the increased renal clearance of circulating solute in critically ill patients. In this study, the analytical research method of transcriptomics combined with metabolomics was used to study the pathogenesis of ARC at the transcriptional and metabolic levels. In transcriptomics, 534 samples from 5 datasets in the Gene Expression Omnibus database were analyzed and 834 differential genes associated with ARC were obtained. In metabolomics, we used Ultra-Performance Liquid Chromatography-Quadrupole Time-of-Flight Mass Spectrometry to determine the non-targeted metabolites of 102 samples after matching propensity scores, and obtained 45 differential metabolites associated with ARC. The results of the combined analysis showed that purine metabolism, arginine biosynthesis, and arachidonic acid metabolism were changed in patients with ARC. We speculate that the occurrence of ARC may be related to the alteration of renal blood perfusion by LTB4R, ARG1, ALOX5, arginine and prostaglandins E2 through inflammatory response, as well as the effects of , , , , NMDAR, glutamate and cAMP on renal capillary wall permeability.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10341629PMC
http://dx.doi.org/10.3390/ijms241310459DOI Listing

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