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
Summary
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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