Related Experiment Video
Updated: Dec 14, 2025

Preliminary Study on Acupuncture Combined with Grain-sized Moxibustion for Treating Rheumatoid Arthritis with Finger Joint Pain
Published on: May 16, 2025
Achieving sustained minimal disease activity with methotrexate in early interleukin 23-driven early psoriatic
Hannah den Braanker1,2, Kim Wervers2, Adriana M C Mus2
1Department of Rheumatology and Clinical Immunology, Maasstad Hospital, Rotterdam, Netherlands.
Objectives:
Methotrexate (MTX) is currently the recommended first-line therapy for treating psoriatic arthritis (PsA), despite lacking clear evidence. No estimates of efficacy of MTX in usual care and no clear MTX responsive clinical or laboratory variables are currently available. This study describes the response to MTX monotherapy in newly diagnosed patients with PsA in usual care. Second, we compared clinical variables and cytokine profiles in patients responding and not responding to MTX monotherapy.
Methods:
We used data collected in the Dutch southwest Early Psoriatic Arthritis cohoRt study to select patients with PsA with oligoarthritis or polyarthritis, and at least 1 year follow-up. We analysed disease activity at 6 months of patients who started MTX monotherapy and still used MTX monotherapy 1 year after diagnosis. Cytokine profiles were determined at baseline and after 3 and 6 months with a bead-based multi-immunoassay.
Results:
We identified 219 patients of which 183 (84%) patients started MTX monotherapy within 6 months after diagnosis. 90 patients used MTX monotherapy throughout the first year of which 44 patients (24%) reached minimal disease activity(MDA) at 6 months, decreasing to 33 patients (18%) after 1 year. Non-responders had significantly higher concentrations of interleukin (IL) 23 and IL-10 before and during MTX therapy.
Conclusions:
Our results showed that only 18% of patients with PsA are in sustained MDA after 1 year of MTX monotherapy and non-responders more often had IL-23-driven disease. Our results indicate the need for more treat-to-target and personalised therapy strategies in PsA.
Insights
Methotrexate (MTX) therapy for psoriatic arthritis (PsA) shows limited sustained efficacy, with only 18% achieving minimal disease activity after one year. Non-responders often exhibit higher IL-23 levels, suggesting a need for personalized treatment strategies.
Area of Science:
- Rheumatology
- Immunology
- Clinical Medicine
Background:
- Methotrexate (MTX) is the standard first-line treatment for psoriatic arthritis (PsA).
- Current evidence for MTX efficacy in routine PsA care is limited.
- Predictors of MTX response in PsA are not well-defined.
Purpose of the Study:
- To evaluate the real-world efficacy of MTX monotherapy in newly diagnosed PsA patients.
- To identify clinical and laboratory variables associated with MTX response in PsA.
- To compare cytokine profiles between MTX responders and non-responders.
Main Methods:
- Analysis of data from the Dutch southwest Early Psoriatic Arthritis cohoRt (EPAR) study.
- Inclusion of PsA patients with oligoarthritis or polyarthritis and at least 1-year follow-up.
- Assessment of disease activity at 6 months and 1 year, with cytokine profiling at baseline, 3, and 6 months.
Main Results:
- 183 out of 219 (84%) PsA patients initiated MTX monotherapy within 6 months.
- Only 18% of patients achieved sustained minimal disease activity (MDA) after 1 year of MTX.
- Non-responders showed significantly higher baseline and on-treatment concentrations of interleukin (IL)-23 and IL-10.
Conclusions:
- Sustained MDA is achieved by a minority (18%) of PsA patients on long-term MTX monotherapy.
- Elevated IL-23 levels may indicate an IL-23-driven disease in non-responding PsA patients.
- Personalized, treat-to-target strategies are crucial for optimizing PsA management.
Related Concept Videos
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents
T Cell Types and Functions
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF
Drugs for Treatment of Crohn's Disease in IBD Using Glucocorticoids
Drugs for Treatment of Ulcerative Colitis in IBD
Therapeutic Drug Monitoring: Affecting Factors

