Rheumatoid arthritis

The effects of suppressing inflammation by tofacitinib may simultaneously improve glycaemic parameters and inflammatory markers in rheumatoid arthritis patients with comorbid type 2 diabetes: a proof-of-concept, open, prospective, clinical study

Arthritis Res TherPublished Prospective single-group clinical study

Main finding · Overall reduction of HOMA2-IRResult — go to the resultβ - 1.1 95% CI - 1.5 to - 0.76

Authors' conclusion

The administration of tofacitinib in RA with T2D led to a simultaneous improvement of IR and inflammatory disease activity, inducing a "bidirectional" benefit in these patients.

Study context

Population
Consecutive rheumatoid arthritis (RA) patients with T2D diagnosisfemale sex 68.9%
Participants
40 patients
Outcome
Change in homeostatic model assessment of IR (HOMA2-IR)
Follow-up
6 months
Methodological detailsproof-of-concept, open, consecutive patients, Planned before the recent emergence of safety signals about tofacitinib
  • Proof-of-concept
  • Open
  • Consecutive patients
  • Planned before the recent emergence of safety signals about tofacitinib

Main finding

Overall reduction of HOMA2-IR

β

- 1.1

95% CI - 1.5 to - 0.76

P = 0.019

As reported in the abstract

Observational data: associations, not effects.

Further findings

HOMA2-β

HOMA2-β enhanced, highlighting an improvement of insulin sensitivity

Glycated haemoglobin

Trend in glycated haemoglobin reduction
  • A longer follow-up is required

RA disease activity

Patients achieving a good clinical response
76.8%
Significant reduction of DAS28-CRP and SDAI

Safety

No major adverse events (AEs), no life-threatening AEs and no cardiovascular and/or thromboembolic events recorded; no new safety signals

Original publication

The effects of suppressing inflammation by tofacitinib may simultaneously improve glycaemic parameters and inflammatory markers in rheumatoid arthritis patients with comorbid type 2 diabetes: a proof-of-concept, open, prospective, clinical study. Arthritis Res Ther. Published 4 January 2024. doi:10.1186/s13075-023-03249-7

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