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Efficacy and Safety of Biologics in Polymyalgia Rheumatica: A Retrospective Study
Naoaki Ohkubo1, Yusuke Miyazaki1, Shingo Nakayamada1
1The First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan, 1-1 Iseigaoka, Yahata-nishi, Kitakyushu, Fukuoka, 807-8555, Japan.
Introduction:
The study aimed to determine the efficacy and safety of biological disease-modifying antirheumatic drugs (bDMARDs) in the treatment of polymyalgia rheumatica (PMR) complicated by rheumatoid arthritis (RA).
Methods:
Patients with PMR which could be classified as RA and who were treated with bDMARDs were included in the analysis. The primary endpoint was the clinical Polymyalgia Rheumatica Activity Score (Clin-PMR-AS) after 26 weeks of treatment, and the secondary endpoint was adverse events during the observation period.
Results:
A total of 203 patients with PMR which was resistant or intolerant to glucocorticoids and could be classified as RA were receiving bDMARDs and were enrolled in the study. There were 83, 82, and 38 patients in the tumor necrosis factor inhibitor (TNFi), interleukin-6 receptor inhibitor (IL-6Ri), and cytotoxic T lymphocyte-associated antigen-4-immunoglobulin (CTLA4-Ig) groups, respectively. Twenty-six weeks after bDMARD initiation, Clin-PMR-AS levels were significantly lower in the IL-6Ri group as compared to other groups. Multiple regression analysis was performed with Clin-PMR-AS as the objective variable. Body mass index (BMI), history of bDMARDs, and IL-6Ri use were identified as factors involved in Clin-PMR-AS. After adjustment for group characteristics using inverse probability of treatment weighting with propensity scores, the Clin-PMR-AS score at 26 weeks was significantly lower in the IL-6Ri group (9.0) than in both the TNFi (12.4, p = 0.004) and CTLA4-Ig (15.9, p = 0.003) group.
Conclusion:
IL-6Ri may potentially improve the disease activity of PMR compared to other bDMARDs.
Insights
Interleukin-6 receptor inhibitors (IL-6Ri) may effectively treat polymyalgia rheumatica (PMR) with rheumatoid arthritis (RA) complications. This study found IL-6Ri significantly reduced disease activity scores compared to other biological disease-modifying antirheumatic drugs (bDMARDs).
Area of Science:
- Rheumatology
- Immunology
- Pharmacology
Background:
- Polymyalgia rheumatica (PMR) can present with rheumatoid arthritis (RA) overlap.
- Glucocorticoid resistance or intolerance is common in PMR/RA cases.
- Biological disease-modifying antirheumatic drugs (bDMARDs) are used for complex PMR/RA.
Purpose of the Study:
- To evaluate the efficacy and safety of bDMARDs in PMR patients with RA.
- To compare different classes of bDMARDs for treating PMR/RA.
- To identify factors influencing treatment outcomes in PMR/RA patients.
Main Methods:
- Analysis of 203 patients with PMR/RA treated with bDMARDs.
- Primary endpoint: Clinical Polymyalgia Rheumatica Activity Score (Clin-PMR-AS) at 26 weeks.
- Secondary endpoint: Adverse events monitoring.
- Comparison of tumor necrosis factor inhibitors (TNFi), IL-6 receptor inhibitors (IL-6Ri), and CTLA4-Ig.
Main Results:
- IL-6Ri use was associated with significantly lower Clin-PMR-AS scores at 26 weeks.
- Compared to TNFi (12.4) and CTLA4-Ig (15.9), IL-6Ri showed a lower mean Clin-PMR-AS (9.0).
- Body mass index, prior bDMARD history, and IL-6Ri use were significant factors in Clin-PMR-AS.
Conclusions:
- Interleukin-6 receptor inhibitors (IL-6Ri) demonstrate potential for improved disease activity in PMR/RA.
- IL-6Ri may be a more effective bDMARD option for PMR patients with RA.
- Further research into IL-6Ri for PMR/RA is warranted.
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