4.4 Article

Metabolic discrimination of synovial fluid between rheumatoid arthritis and osteoarthritis using gas chromatography/time-of-flight mass spectrometry

期刊

METABOLOMICS
卷 18, 期 7, 页码 -

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SPRINGER
DOI: 10.1007/s11306-022-01893-9

关键词

Rheumatoid arthritis; Osteoarthritis; Synovial fluid; Metabolite profiling; Gas chromatography-mass spectrometry

资金

  1. National Research Foundation of Korea - Korean Government (MSIT) [2020R1A2B5B02002631, 2020R1G1A1008268]
  2. Korea Institute of Planning and Evaluation for Technology in Food, Agriculture, Forestry, and Fisheries - Ministry of Agriculture, Food, and Rural Affairs [321036051SB010]
  3. Korea University Food Safety Hall for the Institute of Biomedical Science and Food Safety
  4. Korea University Grant
  5. Institute of Planning & Evaluation for Technology in Food, Agriculture, Forestry & Fisheries (iPET), Republic of Korea [321036051SB010] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  6. National Research Foundation of Korea [2020R1A2B5B02002631, 2020R1G1A1008268] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study assessed the feasibility of using metabolomics to differentiate the metabolite profiles of synovial fluid between rheumatoid arthritis (RA) and osteoarthritis (OA). Results showed clear differences in metabolomic changes between RA and OA, with 28 crucial metabolites identified to play a role in distinguishing the two conditions.
Introduction Rheumatoid arthritis (RA) and osteoarthritis (OA) are clinicopathologically different. Objectives We aimed to assess the feasibility of metabolomics in differentiating the metabolite profiles of synovial fluid between RA and OA using gas chromatography/time-of-flight mass spectrometry. Methods We first compared the global metabolomic changes in the synovial fluid of 19 patients with RA and OA. Partial least squares-discriminant, hierarchical clustering, and univariate analyses were performed to distinguish metabolites of RA and OA. These findings were then validated using synovial fluid samples from another set of 15 patients with RA and OA. Results We identified 121 metabolites in the synovial fluid of the first 19 samples. The score plot of PLS-DA showed a clear separation between RA and OA. Twenty-eight crucial metabolites, including hypoxanthine, xanthine, adenosine, citrulline, histidine, and tryptophan, were identified to be capable of distinguishing RA metabolism from that of OA; these were found to be associated with purine and amino acid metabolism. Conclusion Our results demonstrated that metabolite profiling of synovial fluid could clearly discriminate between RA and OA, suggesting that metabolomics may be a feasible tool to assist in the diagnosis and advance the comprehension of pathological processes for diseases.

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