MicroRNA-125b: association with disease activity and the treatment response of patients with early rheumatoid arthritis
Open Access
- 2 June 2016
- journal article
- research article
- Published by Springer Nature in Arthritis Research & Therapy
- Vol. 18 (1) , 1-8
Abstract
MicroRNAs (miRNAs) are small RNAs that regulate gene expression by targeting mRNA. It was proved that some miRNAs are significantly deregulated in rheumatoid arthritis (RA). MicroRNA-125b negatively regulates expression of TNF-α, which plays a crucial role in RA pathogenesis. The aim of this study was to determine the treatment outcome of patients with early RA based on the expression of circulating and cellular miR-125b. Total RNA was isolated from the plasma and peripheral blood mononuclear cells (PBMCs) of 58 patients with early RA before and three months after treatment initiation and of 54 age- and sex-matched healthy controls (HC). The expression of miR-125b was measured by TaqMan quantitative PCR. The treatment responders were defined as patients achieving remission or low disease activity (28-joint count disease activity score (DAS28) <3.2). Receiver operating characteristic (ROC) curve and stepwise backward multivariable logistic regression analyses of miR-125b expression were used to predict the disease outcome at three and six months after initiation of treatment. The expression of miR-125b in the PBMCs and plasma of treatment-naïve early RA patients was significantly lower than that of HC and increased significantly after three months of treatment, particularly in responders. However, only the cellular expression of miR-125b was inversely correlated with disease activity. MiR-125b expression in PBMCs was higher in responders than in non-responders after three months (p = 0.042). Using ROC analysis, the cellular expression of miR-125b, but not the disease activity at baseline, predicted the treatment response after three months of therapy (area under the curve 0.652 (95 % CI 0.510 to 0.793); p = 0.048). The expression of miR-125b in PBMCs of treatment-naïve patients may present a novel biomarker for monitoring the treatment outcome during the early phase of RA.Keywords
Funding Information
- Ministerstvo Zdravotnictví Ceské Republiky (NT 14498 and 023728)
- Přírodovědecká Fakulta, Univerzita Karlova (GAUK-367615)
- 1. lékařská fakulta v Praze, Univerzita Karlova (SVV 260 155)
This publication has 33 references indexed in Scilit:
- MicroRNAs in Rheumatoid ArthritisBioDrugs, 2012
- microRNA Regulation of Inflammatory ResponsesAnnual Review of Immunology, 2012
- Circulating MiR-125b as a Marker Predicting Chemoresistance in Breast CancerPLOS ONE, 2012
- The microcosmos of cancerNature, 2012
- Novel regulatory mechanisms in inflammatory arthritis: a role for microRNAImmunology & Cell Biology, 2012
- Aggressive therapy in patients with early arthritis results in similar outcome compared with conventional care: the STREAM randomized trialRheumatology, 2011
- Mycobacterium tuberculosislipomannan blocks TNF biosynthesis by regulating macrophage MAPK-activated protein kinase 2 (MK2) and microRNA miR-125bProceedings of the National Academy of Sciences, 2011
- Plasma and synovial fluid microRNAs as potential biomarkers of rheumatoid arthritis and osteoarthritisArthritis Research & Therapy, 2010
- MicroRNAs: Target Recognition and Regulatory FunctionsCell, 2009
- Circulating microRNAs as stable blood-based markers for cancer detectionProceedings of the National Academy of Sciences, 2008