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血清补体 3 水平高是接受托珠单抗治疗的 TA 患者血管狭窄进展的危险因素:一项前瞻性观察研究。

High level of serum complement 3 is a risk factor for vascular stenosis progression in TA patients receiving tocilizumab: a prospective observational study.

机构信息

Department of Rheumatology, Zhongshan Hospital Fudan University, No.180, Fenglin Road, Xuhui District, Shanghai, 200032, China.

Evidence-Based Medicine Centre, Fudan University, Shanghai, China.

出版信息

Arthritis Res Ther. 2023 Aug 2;25(1):137. doi: 10.1186/s13075-023-03106-7.

Abstract

BACKGROUND

The IL-6R antibody tocilizumab has been proven effective in treating Takayasu arteritis (TA). However, some patients show silent vascular stenosis progression (VSP) despite treatment with tocilizumab. The aim of the study was to explore the related risk factors of VSP in patients treated with tocilizumab.

METHODS

Patients receiving tocilizumab were enrolled from the prospective living ongoing East China Takayasu Arteritis cohort. Their medical information was uniformly recorded with a homogenized evaluation method. Magnetic resonant angiography or computed tomographic angiography was employed to monitor VSP during the follow-up period, and Cox regression analysis was performed to explore the related risk factors.

RESULTS

Thirty-eight patients were enrolled, among whom 18 (47.4%) experienced VSP, and seven and three patients experienced new and worsened vascular ischemic symptoms and events (VISE) during follow-up, respectively. The median period for VSP occurrence was 6.9 months during follow-up. Patients with VSP showed higher levels of baseline complement 3 (C3) than those in the patients without VSP. Multivariate Cox regression analysis revealed baseline C3 level (hazard ratio [HR] = 7.05, 95% confidence interval: 1.50-33.07, p = 0.013) was independently associated with VSP, with a cut-off value of 1.22 g/L.

CONCLUSIONS

47.4% of TA patients treated with tocilizumab would suffer VSP. A high C3 level is a risk factor for VSP in TA patients receiving tocilizumab, which may facilitate the option of tocilizumab in the future.

摘要

背景

白细胞介素 6 受体拮抗剂托珠单抗已被证明对治疗大动脉炎(TA)有效。然而,一些患者尽管接受托珠单抗治疗,仍会出现无症状性血管狭窄进展(VSP)。本研究旨在探讨托珠单抗治疗患者 VSP 的相关危险因素。

方法

从前瞻性华东大动脉炎队列中纳入接受托珠单抗治疗的患者。采用统一的评估方法记录他们的医疗信息。在随访期间采用磁共振血管造影或计算机断层血管造影监测 VSP,并进行 Cox 回归分析以探讨相关危险因素。

结果

共纳入 38 例患者,其中 18 例(47.4%)发生 VSP,7 例和 3 例患者在随访期间分别出现新的和加重的血管缺血性症状和事件(VISE)。VSP 发生的中位时间为随访期间 6.9 个月。发生 VSP 的患者基线补体 3(C3)水平高于未发生 VSP 的患者。多因素 Cox 回归分析显示,基线 C3 水平(风险比[HR] = 7.05,95%置信区间:1.50-33.07,p = 0.013)与 VSP 独立相关,其截断值为 1.22 g/L。

结论

接受托珠单抗治疗的 TA 患者中有 47.4%会发生 VSP。高 C3 水平是 TA 患者接受托珠单抗治疗后发生 VSP 的危险因素,这可能有助于未来托珠单抗的选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a547/10394800/9d6db9bc5eec/13075_2023_3106_Fig1_HTML.jpg

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