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Abstract Number: 1134

Efficacy and Safety of Anakinra for Acute Calcium Pyrophosphate Deposition Disease Flare: A Systematic Review and Meta-Analysis

Pannathorn Nakaphan1, Somkiat Phutinart2, Patavee Pajareya2, Priabprat Jansem3, Nattanicha Chaisrimaneepan4, Pim Jetanalin5 and Noppachai Siranart2, 1Department of Internal Medicine, Weiss Memorial Hospital, Chicago, IL, 2Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand, 3Department of Psychiatry, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand, 4Department of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, 5Department of Medicine, Division of Rheumatology, University of Illinois College of Medicine, Chicago, IL

Meeting: ACR Convergence 2025

Keywords: Crystal-induced arthritis, Interleukins, meta-analysis, pseudogout

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Session Information

Date: Monday, October 27, 2025

Title: (1123–1146) Metabolic & Crystal Arthropathies – Basic & Clinical Science Poster I

Session Type: Poster Session B

Session Time: 10:30AM-12:30PM

Background/Purpose: Calcium Pyrophosphate Deposition Disease (CPPD) is a common inflammatory arthritis among older adults. Comorbidities often limit conventional treatment of acute CPPD flare. Anakinra, an interleukin-1 inhibitor, is a promising alternative. We aimed to evaluate the efficacy and safety of anakinra in acute CPPD flares.

Methods: We systematically searched studies from MEDLINE, EMBASE, and the Cochrane Database up until August 2024. The primary outcome was a positive treatment response between day 3 and day 5 after anakinra initiation. Secondary outcomes included changes in pain ratings assessed by the visual analog scales (VAS), C-reactive protein levels, tender joint counts (TJC), swollen joint counts (SJC) and corticosteroid usage.

Results: Six studies were included in our meta-analysis: five observational studies and one randomized controlled trial. A total of 84 patients were included in our analysis. Subjective physician assessments of clinical response were reported in all studies with a combined positive treatment response rate of 76% (95%CI: 61-86, I2=0%). Our pooled analysis also showed a significant reduction of VAS scores by 48.12 mm (95% CI: 53.21 – 43.03, I²=0%) and CRP levels by 62.09 mg/L (95% CI: 97.74-26.44, I²=77%) from baseline. Reductions of TJC and SJC were also demonstrated, 4.86 (95% CI: 5.48 – 4.23, I²=0%) and 3.65 (95% CI: -12.53-5.22, I²=54%), respectively. Adverse reactions included injection site reaction, rash, bacterial pneumonitis, and neutropenia.

Conclusion: Anakinra is a promising alternative treatment for patients with acute CPPD flare as it showed desirable clinical responses and a favorable safety profile.

Supporting image 1Figure 1. The PRISMA Flow Diagram

Supporting image 2Figure 2. Subjective Physician Assessment of Clinical Responses Following Anakinra Treatment for Acute CPPD Flares. The figure depicts the proportion of patients achieving clinical responses as evaluated by physicians after treatment with Anakinra.

Supporting image 3Figure 3. Mean Differences in Secondary Outcomes Following Anakinra Treatment for Acute CPPD Flares. The figure depicts the mean differences in secondary outcomes measured between baseline and post-treatment with Anakinra. Secondary outcomes include: (A) Visual analog scale, (B) Total joint count, (C) Swollen joint count, (D) C-reactive protein levels, and (E) Steroid-sparing effects.


Disclosures: P. Nakaphan: None; S. Phutinart: None; P. Pajareya: None; P. Jansem: None; N. Chaisrimaneepan: None; P. Jetanalin: None; N. Siranart: None.

To cite this abstract in AMA style:

Nakaphan P, Phutinart S, Pajareya P, Jansem P, Chaisrimaneepan N, Jetanalin P, Siranart N. Efficacy and Safety of Anakinra for Acute Calcium Pyrophosphate Deposition Disease Flare: A Systematic Review and Meta-Analysis [abstract]. Arthritis Rheumatol. 2025; 77 (suppl 9). https://acrabstracts.org/abstract/efficacy-and-safety-of-anakinra-for-acute-calcium-pyrophosphate-deposition-disease-flare-a-systematic-review-and-meta-analysis/. Accessed .
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