Tofacitinib and Baricitinib in Type 2 Diabetic Patients with Rheumatoid Arthritis


Por: Martinez-Molina, C, Diaz-Torne, C, Park, HS, Feliu, A, Vidal, S, Corominas, H

Publicada: 1 mar 2024
Resumen:
Background and Objectives: Recently, a randomized controlled trial suggested a potential benefit of baricitinib in patients with diabetes mellitus, preserving beta-cell function. However, the clinical evidence currently available is limited. We aimed to assess the potential impact of tofacitinib and baricitinib on type 2 diabetes mellitus (T2DM) patients with rheumatoid arthritis. Materials and Methods: The candidates for this observational, retrospective, single-center study were selected from a cohort of 120 rheumatoid arthritis patients treated with tofacitinib or baricitinib between September 2017 and September 2023. The eligibility criteria included patients with T2DM who were receiving oral antidiabetic drugs (OADs). The primary outcome was the glycosylated hemoglobin (HbA1c) value after 6 months of a JAK inhibitor treatment. Secondary outcomes included body mass index (BMI) and rheumatoid arthritis disease activity. Differences were evaluated using Fisher's exact test, as well as the Mann-Whitney test or the Wilcoxon test. Results: Thirteen patients were included; 46.2% (6/13) underwent treatment with tofacitinib, while 53.8% (7/13) were treated with baricitinib. At 6 months, baricitinib treatment resulted in a reduction in HbA1c (p = 0.035), with 57.1% (4/7) of patients achieving values <7%, and 28.6% (2/7) of patients requiring a reduction in OAD dosage. Concerning BMI, an increase (p = 0.022) was observed at 6 months following baricitinib administration. All the patients treated with either tofacitinib or baricitinib achieved remission or low disease activity, without requiring statistically significant changes in concomitant rheumatoid arthritis treatment. Conclusions: In T2DM patients with rheumatoid arthritis, baricitinib can improve insulin sensitivity and glucose uptake, enabling the optimization of T2DM management.

Filiaciones:
Martinez-Molina, C:
 Hosp Santa Creu & Sant Pau, Dept Pharm, Barcelona 08041, Spain

 Univ Autonoma Barcelona UAB, Dept Med, Barcelona 08193, Spain

Diaz-Torne, C:
 Univ Autonoma Barcelona UAB, Dept Med, Barcelona 08193, Spain

 Hosp Santa Creu & Sant Pau, Dept Rheumatol & Syst Autoimmune Dis, Barcelona 08041, Spain

Park, HS:
 Univ Autonoma Barcelona UAB, Dept Med, Barcelona 08193, Spain

 Hosp Santa Creu & Sant Pau, Dept Rheumatol & Syst Autoimmune Dis, Barcelona 08041, Spain

Feliu, A:
 Hosp Santa Creu & Sant Pau, Dept Pharm, Barcelona 08041, Spain

Vidal, S:
 Univ Autonoma Barcelona UAB, Dept Med, Barcelona 08193, Spain

 St Pau Biomed Res Inst IIB St Pau, Grp Immunol Inflammatory Dis, Barcelona 08041, Spain

Corominas, H:
 Univ Autonoma Barcelona UAB, Dept Med, Barcelona 08193, Spain

 Hosp Santa Creu & Sant Pau, Dept Rheumatol & Syst Autoimmune Dis, Barcelona 08041, Spain
ISSN: 1010660X
Editorial
MDPI, ST ALBAN-ANLAGE 66, CH-4052 BASEL, SWITZERLAND, Lituania
Tipo de documento: Article
Volumen: 60 Número: 3
Páginas:
WOS Id: 001193344900001
ID de PubMed: 38541086
imagen Green Published, gold

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