Abstract

Although Janus kinase inhibitors (JAKi) could reduce patient-reported pain in rheumatoid arthritis (RA), their mechanism remains unclear. Therefore, we examined lipid metabolites change in JAKi-treated patients and evaluate their association with pain reduction. We used 1H-NMR-based lipid/metabolomics to determine serum levels of lipid metabolites at baseline and week 24 of treatment. Serum levels of significant lipid metabolites were replicated by ELISA in 24 JAKi-treated and 12 tocilizumab-treated patients. Pain was evaluated with patients’ assessment on a 0–100 mm VAS, and disease activity assessed using DAS28. JAKi or tocilizumab therapy significantly reduced disease activity. Acceptable pain (VAS pain ≤20) at week 24 was observed in 66.7% of JAKi-treated patients, and pain decrement was greater than tocilizumab-treated patients (ΔVAS pain 70.0 vs. 52.5, p = 0.0595). Levels of omega-3 fatty acids and docosahexaenoic acid (DHA) were increased in JAKi-treated patients (median 0.55 mmol/L versus 0.71 mmol/L, p = 0.0005; 0.29 mmol/L versus 0.35 mmol/L, p = 0.0004; respectively), which were not observed in tocilizumab-treated patients. ELISA results showed increased DHA levels in JAKi-treated patients with acceptable pain (44.30 µg/mL versus 45.61 µg/mL, p = 0.028). A significant association of pain decrement with DHA change, not with DAS28 change, was seen in JAKi-treated patients. The pain reduction effect of JAKi probably links to increased levels of omega-3 fatty acids and DHA.

Highlights

  • The pain decrement was greater in Janus kinase inhibitors (JAKi)-treated patients than in those treated with TCZ (∆visual analogue scale (VAS) pain 70.0 vs. 52.5, p = 0.0595, Figure 1B)

  • Our results showed a trend of positive correlation between baseline docosahexaenoic acid (DHA) levels from the nuclear magnetic resonance (NMR)-based assay and those from ELISA-based assay (r = 0.327, p = 0.096) in rheumatoid arthritis (RA) patients

  • Given that omega-3 polyunsaturated fatty acids (PUFAs) and DHA showed a beneficial effect of pain reduction [26,30], we examined the changes of their serum levels in RA treated with JAKi or TCZ

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Summary

Introduction

Rheumatoid arthritis (RA) is characterized by inflammation and hyperplasia of synovia, cartilage degradation, and bone erosions [1,2]. A dominant component of the patient-reported outcome, can significantly burden RA patients’ quality of life. Reduction of RA-related pain is one major need of patients [3,4]. Pain associated with RA is multifactorial and complex [5,6,7,8,9,10], and the mechanisms include peripheral joint inflammation, noninflammatory nociceptive stimuli, peripheral/central sensitization, and JAK/STAT pathway [5,6,7,8,9,10].

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