Synovial Joint Fluid Metabolomic Profiles and Pathways Differentiate Osteoarthritis, Rheumatoid Arthritis, and Psoriatic Arthritis

Each arthritis type displayed distinct metabolic fingerprints in synovial fluid. Candidate discriminatory metabolites, including gut-derived metabolites in OA and specific lipid alterations in PsA, open new diagnostic and therapeutic avenues. Given the limited RA sample size (<i>n</i> = 5), RA-related results should be viewed as exploratory and requiring validation in larger independent cohorts. These metabolites may, after rigorous validation in larger and independent cohorts, contribute to multi-metabolite biomarker panels for earlier diagnosis and to the rational design of targeted therapeutics addressing disease-specific metabolic disruptions.

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Publication Details

Journal
Metabolites
Published
2026-01-12
DOI
https://doi.org/10.3390/metabo16010070
Primary Topic
Metabolomics and Mass Spectrometry Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Synovial Joint Fluid Metabolomic Profiles and Pathways Differentiate Osteoarthritis, Rheumatoid Arthritis, and Psoriatic Arthritis

F. Korkusuz, Mustafa Çelebi̇er, OZAN KAPLAN, Rositsa Karalilova et al.
Metabolites
Metabolomics and Mass Spectrometry Studies
article

Synovial Joint Fluid Metabolomic Profiles and Pathways Differentiate Osteoarthritis, Rheumatoid Arthritis, and Psoriatic Arthritis

F. Korkusuz, Mustafa Çelebi̇er, OZAN KAPLAN, Rositsa Karalilova, Z. Batalov, Konstantin Batalov, Victoria Sarafian, Maria Kazakova, Emine Koç
article en

Abstract

Each arthritis type displayed distinct metabolic fingerprints in synovial fluid. Candidate discriminatory metabolites, including gut-derived metabolites in OA and specific lipid alterations in PsA, open new diagnostic and therapeutic avenues. Given the limited RA sample size (<i>n</i> = 5), RA-related results should be viewed as exploratory and requiring validation in larger independent cohorts. These metabolites may, after rigorous validation in larger and independent cohorts, contribute to multi-metabolite biomarker panels for earlier diagnosis and to the rational design of targeted therapeutics addressing disease-specific metabolic disruptions.

MetabolitesVol. 16(1)
Medical University Plovdiv (BG), Hacettepe University (TR)
European Commission, Türkiye Bilimler Akademisi
Reduced inequalities
Openalex Percentile: Top 90%
Metabolomics and Mass Spectrometry Studies
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