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IL-17 抑制剂治疗患者中新发炎症性肠病:来自病例对照 MISSIL 研究的结果。

New-onset inflammatory bowel diseases among IL-17 inhibitor-treated patients: results from the case-control MISSIL study.

机构信息

Service de Rhumatologie, Université de Lille, CHU Lille, Lille.

Service de Rhumatologie, Aix Marseille University, APHM, Marseille.

出版信息

Rheumatology (Oxford). 2022 Jul 6;61(7):2848-2855. doi: 10.1093/rheumatology/keab819.

Abstract

OBJECTIVES

To describe new-onset IBD (new IBD) in patients treated with IL-17 inhibitors (IL-17i), to assess their incidence and to identify their risk factors in real life.

METHODS

A French national registry (MISSIL) aimed to report all cases of new IBD in patients treated with IL-17i from January 2016 to December 2019. Using the estimated number of patients treated by IL-17 in France during the study period, the annual incidence rates of new IBD was reported in IL-17i-treated patients. A case-control study was performed with two controls per new IBD case matched by gender, age and underlying inflammatory disease.

RESULTS

Thirty-one cases of new IBD under IL-17i were collected: 27 patients treated for spondyloarthritis and four patients for psoriasis. All were observed with secukinumab (SEK). The median time to onset of new IBD symptoms was 4.0 (1.5-7.5) months. SEK was discontinued in all patients. The evolution was favourable with complete resolution (17/31), improvement (7/31) or stabilization (5/31). Two patients died: one due to a massive myocardial infarction and one due to post-colectomy complications. The incidence of new IBD decreased from 0.69/100 patient-years [PY] (7/1010) in 2016 to 0.08/100 PY (6/7951) in 2019. No previous treatment with etanercept (odds ratio [OR] = 0.33, 95% CI: 0.14-0.80, P = 0.014) and low number of previous biologic therapies (OR = 0.67, 95% CI: 0.47, 0.94, P = 0.021) were significantly associated with new IBD.

CONCLUSION

The incidence of new IBD was low and decreased from 2016 to 2019. The outcome was favourable in 24 out of 31 patients, but two patients died.

摘要

目的

描述接受白细胞介素 17 抑制剂(IL-17i)治疗的患者中新发炎症性肠病(new IBD)的情况,评估其发病率,并确定其在真实世界中的风险因素。

方法

法国国家登记处(MISSIL)旨在报告 2016 年 1 月至 2019 年 12 月期间接受 IL-17i 治疗的患者中新发 IBD 的所有病例。根据研究期间法国接受 IL-17i 治疗的患者估计数量,报告了接受 IL-17i 治疗的患者中新发 IBD 的年发病率。采用每例新 IBD 患者匹配 2 名对照的病例对照研究,匹配性别、年龄和潜在炎症性疾病。

结果

共收集了 31 例接受 IL-17i 治疗的新 IBD 病例:27 例患者接受治疗用于治疗脊柱关节炎,4 例患者用于治疗银屑病。所有患者均接受司库奇尤单抗(SEK)治疗。新发 IBD 症状的中位发病时间为 4.0(1.5-7.5)个月。所有患者均停用 SEK。病情转归良好,完全缓解(17/31)、改善(7/31)或稳定(5/31)。2 例患者死亡:1 例死于大面积心肌梗死,1 例死于结肠切除术后并发症。2016 年新 IBD 的发病率为 0.69/100 患者年(7/1010),2019 年降至 0.08/100 患者年(6/7951)。与新 IBD 显著相关的因素有:无依那西普(OR=0.33,95%CI:0.14-0.80,P=0.014)和生物制剂治疗数量较少(OR=0.67,95%CI:0.47,0.94,P=0.021)。

结论

新 IBD 的发病率较低,且从 2016 年到 2019 年呈下降趋势。31 例患者中有 24 例转归良好,但有 2 例患者死亡。

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