Abstract

In this study, we analysed the expression level of sera circulating miRNA-5196 in rheumatoid arthritis (RA) and ankylosing spondylitis (AS) patients before and after tumor necrosis factor (TNF)-α therapy as biomarkers predicting positive treatment outcome. We enrolled 10 RA patients, 13 AS patients, and 12 healthy individuals in the study. The expression of miRNA-5196 was measured by real-time polymerase chain reaction before and after anti-TNF-α therapy. Disease activity of RA patients was assessed using disease activity score 28 (DAS28), whereas ankylosing spondylitis DAS (ASDAS) was used in AS patients. MiRNA-5196 expression was significantly higher in patients with RA and AS before TNF-α therapy than in those following anti-TNF-α therapy and healthy controls. Changes in miRNA-5196 expression positively correlated with delta DAS28 or delta ASDAS, respectively, following TNF-α therapy. In contrast, changes in C-reactive protein (CRP) levels in RA and AS patients did not positively correlate with DAS28 or ASDAS changes. Receiver-operating characteristic analysis showed better diagnostic accuracy of miRNA-5196 expression both in RA (area under curve (AUC) = 0.87, p = 0.055) and AS patients (AUC = 0.90, p = 0.050) compared to CRP levels in RA (AUC = 0.75, p = 0.201) and AS patients (AUC = 0.85, p = 0.086) upon biologic therapy treatment. Finding novel biomarkers, including miRNA-5196 which allow to predict and monitor anti-TNF-α response, would be of clinical value especially during the early phase of RA or AS development.

Highlights

  • Rheumatic diseases, including rheumatoid arthritis (RA), systemic sclerosis (SSc), or ankylosing spondylitis (AS), are chronic autoimmune disorders characterized by pain and joint inflammation (Ciechomska and O’Reilly 2016)

  • Since we have previously demonstrated that the level of miRNA-5196 is increased in sera and monocytes isolated from SSc patients compared to healthy control (HC) (Ciechomska et al 2017), we sought to investigate the level of miRNA-5196 in sera from RA and AS patients to determine whether circulating miRNA-5196 can be used as a potential biomarker of rheumatic diseases

  • This suggests that expression of circulating miRNA-5196 from patients suffering from rheumatic diseases including SSc, RA and AS is significantly elevated and it can be reduced by anti-tumor necrosis factor (TNF)-α treatment

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Summary

Introduction

Rheumatic diseases, including rheumatoid arthritis (RA), systemic sclerosis (SSc), or ankylosing spondylitis (AS), are chronic autoimmune disorders characterized by pain and joint inflammation (Ciechomska and O’Reilly 2016). Rheumatic diseases affect more individuals than any other disease group (eular.org https://www.eular.org/myUploadData/files/10%20things%20 on%20RD.pdf). A third of people of all ages are affected by rheumatic diseases at some point during their lifetime (eular.org https://www.eular.org/myUploadData/ files/10%20things%20on%20RD.pdf). Rheumatic diseases tend to be progressive in terms of disability; during the last decade, the economic burden of rheumatic diseases has been increasingly recognised. The cost of rheumatic diseases is estimated at more than 200 billion euros per year in Europe (eular.org https://www.eular.org/myUploadData/files/ 10%20things%20on%20RD.pdf).

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