Difficult-to-treat axial spondyloarthritis patients

Abstract

Objectives: This study aimed to formulate D2T (difficult to treat) criteria for axial spondyloarthritis (AxSpA) patients and identify the prevalence of D2T patients and their characteristics.

Patients and methods: The cross-sectional study was conducted with 166 AxSpA patients (93 males, 73 females; mean age: 47.1±12.9 years; range, 19 to 78 years) between February 2023 and March 2023. The criteria were based on patients treated according to the European Alliance of Associations for Rheumatology (EULAR) recommendations for AxSpA. Entry criteria were treatment failure to ≥2 biological/targeted synthetic disease-modifying antirheumatic drugs with two different mechanisms of action or ≥3 biological/targeted synthetic disease-modifying antirheumatic drugs. Potential preliminary factors for D2T criteria were analyzed, and the characteristics of the subjects matching D2T criteria were compared with those of others.

Results: One hundred forty-two ankylosing spondylitis patients and 24 nonradiographic AxSpA patients were included in the study. The rate of fulfilling the D2T criteria was 22.9% (n=38) among AxsPA patients treated with biological agents. The potential D2T criteria were met by 23.2% of ankylosing spondylitis and 20.8% of nonradiographic AxSpA patients. Baseline characteristics, such as sex, age, diagnosis age, occupation, and education, of D2T patients were not statistically different from other patients. The prevalence of fibromyalgia was higher in D2T patients (p<0.001). Disease activity indices and acute phase response indicators were higher and quality of life was worse in D2T patients.

Conclusion: There was a considerable amount of AxSpA patients fulfilling the D2T criteria despite new and effective treatment agents.

Citation: Öğüt TS, Erbasan F, Şahiner MF, Nokay M, Yörük Öğüt A, Dilbil M, et al. Difficult-totreat axial spondyloarthritis patients. Arch Rheumatol 2024;39(3):419-428. doi: 10.46497/ ArchRheumatol.2024.10567.

The study protocol was approved by the Akdeniz University Faculty of Medicine Clinical Research Ethics Committee (date: 08.02.2023, no: KAEK-97). The study was conducted in accordance with the principles of the Declaration of Helsinki.

A written informed consent was obtained from each patient.

Have designed the study: V.Y., T.S.Ö.; Have collected the data: T.S.Ö., M.N., M.D., M.F.., A.Y.Ö.; Data analyses and interpretation have been performed: V.Y., T.S.Ö.; Literature review is done: T.S.Ö., F.E.; Have written the first draft of the manuscript, and all authors commented on the last version of the manuscript: V.Y., T.S.Ö.; Critical review of the manuscript is performed: M.E.T. All authors have read and approved the final and revised manuscript.

The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

The authors received no financial support for the research and/or authorship of this article.

The data that support the findings of this study are available from the corresponding author upon reasonable request.