医学                        
                
                                
                        
                            内科学                        
                
                                
                        
                            类风湿性关节炎                        
                
                                
                        
                            中止                        
                
                                
                        
                            危险系数                        
                
                                
                        
                            比例危险模型                        
                
                                
                        
                            队列                        
                
                                
                        
                            Janus激酶抑制剂                        
                
                                
                        
                            不利影响                        
                
                                
                        
                            回顾性队列研究                        
                
                                
                        
                            胃肠病学                        
                
                                
                        
                            托法替尼                        
                
                                
                        
                            置信区间                        
                
                        
                    
            作者
            
                Ryu Watanabe,Kosuke Ebina,Takaho Gon,Tadashi Okano,Koichi Murata,Kosaku Murakami,Yuichi Maeda,Sadao Jinno,Iku Shirasugi,Yonsu Son,Hideki Amuro,Masaki Katayama,Ryota Hara,Kenichiro Hata,Ayaka Yoshikawa,Wataru Yamamoto,Shotaro Tachibana,Shinya Hayashi,Yuki Etani,Masao Katsushima            
         
                    
            出处
            
                                    期刊:Rheumatology
                                                         [Oxford University Press]
                                                        日期:2024-05-09
                                                        卷期号:63 (9): 2418-2426
                                                        被引量:4
                                 
         
        
    
            
            标识
            
                                    DOI:10.1093/rheumatology/keae265
                                    
                                
                                 
         
        
                
            摘要
            
            Abstract Objectives To investigate the predictive factors for difficult-to-treat rheumatoid arthritis (D2T RA) and assess the efficacy of biologic DMARDs (bDMARDs) and Janus kinase inhibitors (JAKi). Methods Retrospective analysis was conducted on data from the ANSWER cohort comprising 3623 RA patients treated with bDMARDs or JAKi in Japan. Multivariate Cox proportional hazards modelling was used to analyse the hazard ratios (HRs) for treatment retention. Results Of the 3623 RA patients, 450 (12.4%) met the first two criteria of the EULAR D2T RA definition (defined as D2T RA in this study). Factors contributing to D2T RA included age over 75 (compared with those under 65, hazard ratio [HR] = 0.46; 95% CI: 0.31, 0.69), higher rheumatoid factor (RF) titres (HR = 1.005; 95% CI: 1.00, 1.01), higher clinical disease activity index (HR = 1.02; 95% CI: 1.01, 1.03), lower methotrexate dosage (HR = 0.97; 95% CI: 0.95, 0.99), and comorbidities like hypertension (HR = 1.53; 95% CI: 1.2, 1.95) and diabetes (HR = 1.37; 95% CI: 1.09, 1.73). Anti-IL-6 receptor antibodies (aIL-6R, HR = 0.53; 95% CI: 0.37, 0.75) and JAKi (HR = 0.64; 95% CI: 0.46, 0.90) were associated with fewer discontinuations due to ineffectiveness compared with TNF inhibitors. Oral glucocorticoid usage (HR = 1.65; 95% CI: 1.11, 2.47) was linked to increased discontinuation due to toxic adverse events. Conclusion Younger onset, higher RF titres, and comorbidities predicted D2T RA development. For managing D2T RA, aIL-6R and JAKi exhibited superior drug retention.
         
            
 
                 
                
                    
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