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Front Immunol ; 12: 638066, 2021.
Article in English | MEDLINE | ID: mdl-34177888

ABSTRACT

There is an urgent need to identify biomarkers for diagnosis and disease activity monitoring in rheumatoid arthritis (RA). We leveraged publicly available microarray gene expression data in the NCBI GEO database for whole blood (N=1,885) and synovial (N=284) tissues from RA patients and healthy controls. We developed a robust machine learning feature selection pipeline with validation on five independent datasets culminating in 13 genes: TNFAIP6, S100A8, TNFSF10, DRAM1, LY96, QPCT, KYNU, ENTPD1, CLIC1, ATP6V0E1, HSP90AB1, NCL and CIRBP which define the RA score and demonstrate its clinical utility: the score tracks the disease activity DAS28 (p = 7e-9), distinguishes osteoarthritis (OA) from RA (OR 0.57, p = 8e-10) and polyJIA from healthy controls (OR 1.15, p = 2e-4) and monitors treatment effect in RA (p = 2e-4). Finally, the immunoblotting analysis of six proteins on an independent cohort confirmed two proteins, TNFAIP6/TSG6 and HSP90AB1/HSP90.


Subject(s)
Arthritis, Rheumatoid/pathology , Cell Adhesion Molecules/metabolism , HSP90 Heat-Shock Proteins/metabolism , Osteoarthritis/pathology , Synovial Membrane/metabolism , Biomarkers/metabolism , Cell Adhesion Molecules/genetics , Disease Progression , Gene Expression Profiling , HSP90 Heat-Shock Proteins/genetics , Humans , Machine Learning , Transcriptome/genetics
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