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COMPARISON OF EFFICACY AND SAFETY OF DIFFERENT MEDICATION PROTOCOLS IN PATIENTS WITH IMMUNOGLOBULIN G4-RELATED DISEASE BASED ON FOLLOW-UP TIME: A SYSTEMATIC REVIEW AND NETWORK META-ANALYSIS

Yanwen LIU, Xianghui FU, Youqun ZHANG, Yan ZHENG, Junfeng JIA, Ping ZHU, Kui ZHANG

Archives of Rheumatology - 2026;41(1):3-13

Department of Clinical Immunology, Xijing Hospital, Fourth Military Medical University, Xi'an, China

 

Background/Aims: Glucocorticoids (GCs) and disease-modifying anti-rheumatic drugs (DMARDs) are commonly used drugs in the treatment of immunoglobulin G4-related disease (IgG4-RD). However, no broad consensus is available on their intervention effects. Therefore, the efficacy and safety of different medication protocols in the treatment of IgG4-RD were assessed in this systematic review and network meta-analysis. Materials and Methods: This study was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses. RStudio and Stata 15.1 were used for data analysis. Results: The results showed that in terms of improvement of remission rates, GCs + DMARDs had the strongest overall efficacy [surface under the cumulative ranking curve (SUCRA) = 82.9%], and DMARDs were the most effective within 12 months during follow-up (SUCRA = 82.5%), while GCs + DMARDs were the most effective over 12 months during follow-up (SUCRA = 83.2%). In terms of reduction of relapse rates, the overall efficacy of GCs + DMARDs was the strongest (SUCRA = 83.5%), and GCs + DMARDs performed the best both within and over 12 months during follow-up. The adverse reaction rates were 38.9%, 5.3%, and 33.3%, respectively, among patients treated with GCs + DMARDs, DMARDs, and GCs. Conclusion: The GCs + DMARDs are recommended for short-term improvement of remission rates and reduction of relapse rates, as well as for achieving long-term efficacy.