Department of Medical Science, BK21 Plus Project, Yonsei University, College of Medicine, Seoul, Korea (Republic of).
Division of Rheumatology, Department of Internal Medicine, Yongin Severance Hospital, Yonsei University College of Medicine, 363 Dongbaekjukjeon-daero, Giheung-gu, 16995, Yongin, Gyeonggi-do, Korea (Republic of).
Z Rheumatol. 2024 Feb;83(Suppl 1):230-235. doi: 10.1007/s00393-023-01320-x. Epub 2023 Feb 2.
This study investigated whether circulating cold-inducible RNA-binding protein (CIRP) could be a biomarker to reflect the current activity, function, and damage status in patients with microscopic polyangiitis (MPA) and granulomatosis with polyangiitis (GPA).
This study selected 39 MPA and 26 GPA patients. Antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV)-specific indices include the Birmingham Vasculitis Activity Index (BVAS), five-factor score (FFS), the Korean version of the Short-Form 36-Item Health Survey (SF-36) physical component summary (PCS) and mental component summary (MCS), and the vasculitis damage index (VDI). The highest tertile of BVAS was defined as high activity of AAV.
The median age of the study subjects was 65.0 years and 53.8% were women. The median BVAS, FFS, SF-36 PCS, MCS, and VDI scores were 12.0, 2.0, 47.5, 50.3, and 3.0, respectively. The median circulating CIRP level was 6.4 ng/mL. Among the four AAV-specific indices, circulating CIRP was significantly correlated with BVAS (r = 0.256). Using the receiver operator characteristic curve, the cut-off of circulating CIRP for high activity of AAV was 6.16 ng/mL. High activity of AAV was identified more frequently in patients with circulating CIRP ≥ 6.16 ng/mL than in those with circulating CIRP < 6.16 ng/mL (48.6% vs. 21.4%). In addition, patients with circulating CIRP ≥ 6.16 ng/mL exhibited a significantly higher risk for high activity of AAV than those with circulating CIRP < 6.16 ng/mL (relative risk 3.474).
This study suggests the clinical potential of circulating CIRP as a biomarker for reflecting the current BVAS and predicting high activity of AAV in patients with MPA and GPA.
本研究旨在探讨循环冷诱导 RNA 结合蛋白(CIRP)是否可作为反映显微镜下多血管炎(MPA)和肉芽肿性多血管炎(GPA)患者当前活动、功能和损伤状态的生物标志物。
本研究纳入了 39 例 MPA 患者和 26 例 GPA 患者。抗中性粒细胞胞质抗体(ANCA)相关性血管炎(AAV)特异性指标包括伯明翰血管炎活动指数(BVAS)、五因子评分(FFS)、韩国版 36 项简明健康状况调查问卷(SF-36)生理成分综合评分(PCS)和心理成分综合评分(MCS)以及血管炎损伤指数(VDI)。将 BVAS 的最高三分位数定义为 AAV 高活动。
研究对象的中位年龄为 65.0 岁,53.8%为女性。中位 BVAS、FFS、SF-36 PCS、MCS 和 VDI 评分为 12.0、2.0、47.5、50.3 和 3.0,中位循环 CIRP 水平为 6.4ng/ml。在四个 AAV 特异性指标中,循环 CIRP 与 BVAS 显著相关(r=0.256)。采用受试者工作特征曲线,循环 CIRP 诊断 AAV 高活动的截断值为 6.16ng/ml。循环 CIRP≥6.16ng/ml 的患者中 AAV 高活动的发生率显著高于循环 CIRP<6.16ng/ml 的患者(48.6% vs. 21.4%)。此外,循环 CIRP≥6.16ng/ml 的患者发生 AAV 高活动的风险显著高于循环 CIRP<6.16ng/ml 的患者(相对风险 3.474)。
本研究提示循环 CIRP 具有作为反映当前 BVAS 和预测 MPA 和 GPA 患者 AAV 高活动的生物标志物的临床潜力。