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Obesity might not alter tofacitinib drug survival in rheumatoid arthritis patients.

Authors :
Kayacan Erdoğan E
Armağan B
Koçak Ulucaköy R
Orhan K
Can Güven S
Özdemir Ulusoy B
Konak HE
Karakaş Ö
Akyüz Dağlı P
Atalar E
Doğan İ
Maraş Y
Omma A
Küçükşahin O
Erten Ş
Babaoğlu H
Source :
Wiener klinische Wochenschrift [Wien Klin Wochenschr] 2024 Sep 11. Date of Electronic Publication: 2024 Sep 11.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Introduction: Obese rheumatoid arthritis (RA) patients often show reduced responses to traditional treatments, including TNF inhibitors (TNFi). Considering the different mechanisms of action it is important to evaluate the efficacy of tofacitinib in obese patients. This study aims to explore the impact of obesity on the drug survival of tofacitinib in RA patients.<br />Material and Methods: This retrospective cohort study included RA patients treated with tofacitinib. Patients were categorized into obese (BMI ≥ 30 kg/m <superscript>2</superscript> ) and non-obese (BMI < 30 kg/m <superscript>2</superscript> ) groups. The primary outcome was drug survival, assessed using Kaplan-Meier and logistic regression analyses.<br />Results: The study comprised 80 RA patients, with 31 (39%) classified as obese. At the 12-month mark, the drug survival rate for tofacitinib was higher in the obese group (81%) compared to the non-obese group (59%). Contrary to univariable analysis, multivariate analysis did not identify obesity as a significant predictor of drug survival. Other variables including sex, hypertension, diabetes mellitus, and anti-cyclic citrullinated peptide (anti-CCP) positivity also showed no significant association with tofacitinib drug survival.<br />Conclusion: The findings indicate that obesity does not alter the drug survival rate for tofacitinib among RA patients. Univariate analysis reported a potentially higher drug survival rate in obese patients; however, the lack of statistical significance in multivariate analysis and the study's retrospective nature necessitate further research to validate these observations and guide personalized therapeutic strategies for this population.<br /> (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature.)

Details

Language :
English
ISSN :
1613-7671
Database :
MEDLINE
Journal :
Wiener klinische Wochenschrift
Publication Type :
Academic Journal
Accession number :
39259223
Full Text :
https://doi.org/10.1007/s00508-024-02424-3