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A very early clinical response to treatment with the Janus kinase inhibitor tofacitinib in patients with active rheumatoid arthritis: the dynamics of pain and central sensitization elements

Authors :
A. E. Karateev
E. S. Filatova
E. Yu. Pogozheva
V. N. Amirdzhanova
E. L. Nasonov
A. M. Lila
V. I. Mazurov
A. Yu. De
A. A. Baranov
N. A. Lapkina
G. V. Lukina
N. A. Kiryukhina
S. Yu. Davidyan
T. S. Salnikova
R. R. Samigullina
D. S. Chakieva
I. M. Marusenko
O. V. Semagina
M. Yu. Semchenkova
A. F. Davydova
E. V. Kalinina
Source :
Современная ревматология, Vol 14, Iss 2, Pp 69-75 (2020)
Publication Year :
2020
Publisher :
IMA-PRESS LLC, 2020.

Abstract

Janus kinase (JK) inhibitors block the intracellular signaling pathways that are responsible for the synthesis of proinflammatory cytokines and mediators, which in turn cause the activation of pain receptors and central sensitization (CS). It is suggested that JK inhibitors can rapidly eliminate pain and reduce the severity of CS.Objective: to evaluate the effect of the JK inhibitor tofacitinib (TOFA) on the intensity of pain and the signs of CS in patients with active rheumatoid arthritis (RA) at 7 and 28 days after therapy initiation.Patients and methods. A study group consisted of 39 patients (79.5% female) (mean age 50.9±11.1 years) with RA (DAS28 5.8±0.6). Of these, 89.7% were seropositive for rheumatoid factor; 82.0% took methotrexate and 18.0% received leflunomide. All the patients were prescribed TOFA 5 mg twice daily due to the inefficacy or intolerance of biological agents. The investigators estimated pain intensity using a Brief Pain Inventory (BPI), rated the presence of a neuropathic pain component (NPC) with the PainDETECT questionnaire, and assessed the signs of CS with the Central Sensitization Inventory (CSI) during the first 4 weeks after TOFA administration.Results and discussion. The patients initially experienced moderate or severe pain (the mean scores of 5.33±2.51 on the numerical rating scale (NRS) included in BPI); 53.8% had signs of CS (CSI scores of ≥40); 17.9% had signs of a NPC (PainDETECT scores of >18). Already on day 7 after the start of TOFA administration, there was a statistically significant decrease in the mean NRS pain intensity scores to 4.06±2.2 (p=0.01) and by 29.4±17.9%, as shown by the patient's assessment of the analgesic effect of therapy (BPI), as well as the severity of CS, namely a decrease in the mean NRS pain score to 35.9±11.2 (p=0.01). On 28 days, the effect became better: there was a reduction in the level of NRS pain to 2.32±1.57 (p

Details

Language :
Russian
ISSN :
19967012 and 2310158X
Volume :
14
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Современная ревматология
Publication Type :
Academic Journal
Accession number :
edsdoj.f84c1d6e4e34c688e41f9ab87acd8f6
Document Type :
article
Full Text :
https://doi.org/10.14412/1996-7012-2020-2-69-75