Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Department of Biomedical Statistics and Bioinformatics, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Arthritis Res Ther. 2022 May 30;24(1):127. doi: 10.1186/s13075-022-02810-0.
Although the survival rates of patients with relapsing polychondritis (RP) have increased remarkably, the high recurrence rate remains a significant concern for physicians and patients. This retrospective study aimed to investigate the risk factors for RP recurrence.
Patients with RP who presented to Kyoto University Hospital from January 2000 to March 2020 and fulfilled Damiani's classification criteria were included. Patients were classified into recurrence and non-recurrence groups. Risk factors for RP recurrence were analysed using a Cox proportional hazards model, and Kaplan-Meier survival curves were drawn.
Thirty-four patients were included. Twenty-five patients (74%) experienced 64 recurrences (mean: 2.56 recurrences per patient). The median duration before the first recurrence was 202 [55-382] days. The median prednisolone dose at the initial recurrence was 10 [5-12.75] mg/day. Tracheal involvement was significantly more frequent in the recurrence group at the initial presentation (44.0% vs. 0.0%, p=0.0172) than in the non-recurrence group, and pre-treatment C-reactive protein levels were significantly higher in the recurrence group than in the non-recurrence group (4.7 vs 1.15 mg/dL, p=0.0024). The Cox proportional hazards model analysis revealed that tracheal involvement (hazard ratio [HR] 4.266 [1.535-13.838], p=0.0048), pre-treatment C-reactive protein level (HR 1.166 [1.040-1.308], p=0.0085), and initial prednisolone monotherapy (HR 4.443 [1.515-16.267], p=0.0056) may be associated with recurrence. The median time before the initial recurrence was significantly longer in patients who received combination therapy with prednisolone and immunosuppressants or biologics (400 vs. 70 days, p=0.0015).
Tracheal involvement, pre-treatment C-reactive protein level, and initial prednisolone monotherapy were risk factors for recurrence in patients with RP. Initial combination therapy with prednisolone and immunosuppressants may delay recurrence.
尽管复发性多软骨炎(RP)患者的生存率显著提高,但高复发率仍是医生和患者关注的重要问题。本回顾性研究旨在探讨 RP 复发的危险因素。
纳入 2000 年 1 月至 2020 年 3 月期间在京都大学医院就诊并符合达米亚尼分类标准的 RP 患者。将患者分为复发组和未复发组。采用 Cox 比例风险模型分析 RP 复发的危险因素,并绘制 Kaplan-Meier 生存曲线。
共纳入 34 例患者。25 例(74%)患者发生 64 次复发(平均每位患者 2.56 次复发)。首次复发前的中位时间为 202[55-382]天。首次复发时,泼尼松的中位剂量为 10[5-12.75]mg/天。初次就诊时,复发组的气管受累明显多于未复发组(44.0% vs. 0.0%,p=0.0172),且复发组治疗前 C 反应蛋白(CRP)水平明显高于未复发组(4.7 vs 1.15mg/dL,p=0.0024)。Cox 比例风险模型分析显示,气管受累(风险比 [HR] 4.266[1.535-13.838],p=0.0048)、治疗前 CRP 水平(HR 1.166[1.040-1.308],p=0.0085)和初始泼尼松单药治疗(HR 4.443[1.515-16.267],p=0.0056)可能与复发有关。接受泼尼松和免疫抑制剂或生物制剂联合治疗的患者首次复发前的中位时间明显长于接受泼尼松单药治疗的患者(400 天 vs. 70 天,p=0.0015)。
气管受累、治疗前 CRP 水平和初始泼尼松单药治疗是 RP 患者复发的危险因素。初始泼尼松和免疫抑制剂联合治疗可能会延迟复发。