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炎症性疾病儿童使用肿瘤坏死因子抑制剂相关的银屑病。

Psoriasis Associated With Tumor Necrosis Factor Inhibitors in Children With Inflammatory Diseases.

机构信息

Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, and Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee.

Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia.

出版信息

Arthritis Care Res (Hoboken). 2021 Feb;73(2):215-220. doi: 10.1002/acr.24100. Epub 2021 Jan 3.

Abstract

OBJECTIVE

To estimate the incidence rate (IR) of psoriasis in children with inflammatory bowel disease (IBD), juvenile idiopathic arthritis (JIA), and chronic noninfectious osteomyelitis (CNO) with tumor necrosis factor inhibitor (TNFi) exposure as compared to children without TNFi exposure and to the general pediatric population.

METHODS

This was a single-center retrospective cohort study of children with IBD, JIA, or CNO from 2008 to 2018. TNFi exposure was defined as a prescription for adalimumab, etanercept, infliximab, certolizumab, or golimumab, and the primary outcome was incident psoriasis. IRs and standardized incidence ratios (SIRs) were calculated. Cox proportional hazards models were used to assess the association of psoriasis with TNFi exposure and other risk factors.

RESULTS

Of the 4,111 children who met inclusion criteria, 1,614 (39%) had TNFi exposure and 2,497 (61%) did not, with 4,705 and 6,604 person-years of follow-up, respectively. There were 58 cases (IR 12.3 per 1,000 person-years) and 25 cases (IR 3.8 per 1,000 person-years) of psoriasis in children with and without TNFi exposure, respectively. The SIR was 18 (95% confidence interval [95% CI] 15-22) overall, 30 (95% CI 23-39) for children with TNFi exposure, and 9.3 (95% CI 6.3-14) for children without TNFi exposure. The hazard ratio of psoriasis comparing TNFi exposure to no TNFi exposure was 3.84 (95% CI 2.28-6.47; P < 0.001).

CONCLUSION

Children with IBD, JIA, and CNO had an increased rate of psoriasis compared to the general pediatric population, with the highest rate in those with TNFi exposure.

摘要

目的

评估在接受肿瘤坏死因子抑制剂(TNFi)治疗的炎症性肠病(IBD)、幼年特发性关节炎(JIA)和慢性非感染性骨髓炎(CNO)患儿中,与未接受 TNFi 治疗的患儿以及一般儿科人群相比,患有银屑病的发生率(IR)。

方法

这是一项 2008 年至 2018 年期间在 IBD、JIA 或 CNO 患儿中进行的单中心回顾性队列研究。TNFi 暴露定义为接受阿达木单抗、依那西普、英夫利昔单抗、certolizumab 或戈利木单抗的处方,主要结局为新发银屑病。计算发病率和标准化发病率比(SIR)。Cox 比例风险模型用于评估银屑病与 TNFi 暴露和其他危险因素的关联。

结果

在符合纳入标准的 4111 名儿童中,1614 名(39%)有 TNFi 暴露,2497 名(61%)没有,分别随访 4705 和 6604 人年。有 58 例(IR 为 12.3/1000 人年)和 25 例(IR 为 3.8/1000 人年)银屑病患儿在有和没有 TNFi 暴露的患儿中,SIR 分别为 18(95%CI 15-22)、30(95%CI 23-39)和 9.3(95%CI 6.3-14)。与无 TNFi 暴露相比,TNFi 暴露患儿发生银屑病的风险比为 3.84(95%CI 2.28-6.47;P<0.001)。

结论

与一般儿科人群相比,IBD、JIA 和 CNO 患儿银屑病的发生率增加,而 TNFi 暴露患儿的发生率最高。

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