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Tumor necrosis factor-α inhibitor-induced psoriasis in juvenile idiopathic arthritis patients.肿瘤坏死因子-α抑制剂诱发幼年特发性关节炎患者出现银屑病。
Pediatr Dermatol. 2019 Sep;36(5):613-617. doi: 10.1111/pde.13859. Epub 2019 Jun 25.
2
Infliximab Paradoxical Psoriasis in a Cohort of Children With Inflammatory Bowel Disease.一组炎症性肠病患儿中的英夫利昔单抗反常性银屑病
J Pediatr Gastroenterol Nutr. 2019 Aug;69(2):189-193. doi: 10.1097/MPG.0000000000002349.
3
Case series of psoriasis associated with tumor necrosis factor-α inhibitors in children with chronic recurrent multifocal osteomyelitis.慢性复发性多灶性骨髓炎患儿中与肿瘤坏死因子-α抑制剂相关的银屑病病例系列
JAAD Case Rep. 2018 Sep 14;4(8):767-771. doi: 10.1016/j.jdcr.2018.06.008. eCollection 2018 Sep.
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Dermatological Manifestations in Pediatric Patients with Inflammatory Bowel Diseases on Anti-TNF Therapy.抗 TNF 治疗的炎症性肠病儿科患者的皮肤表现。
Inflamm Bowel Dis. 2018 Aug 16;24(9):2086-2092. doi: 10.1093/ibd/izy112.
5
Psoriasis and Psoriasiform Eruptions in Pediatric Patients with Inflammatory Bowel Disease Treated with Anti-Tumor Necrosis Factor Alpha Agents.接受抗肿瘤坏死因子α制剂治疗的炎症性肠病儿科患者中的银屑病和银屑病样皮疹
Pediatr Dermatol. 2017 May;34(3):253-260. doi: 10.1111/pde.13081. Epub 2017 Feb 17.
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Development of psoriasis in IBD patients under TNF-antagonist therapy is associated neither with anti-TNF-antagonist antibodies nor trough levels.炎症性肠病(IBD)患者在接受肿瘤坏死因子(TNF)拮抗剂治疗时银屑病的发生既与抗TNF拮抗剂抗体无关,也与谷浓度无关。
Scand J Gastroenterol. 2016 Dec;51(12):1482-1488. doi: 10.1080/00365521.2016.1218541. Epub 2016 Aug 18.
7
Incidence, Clinical Characteristics, and Management of Psoriasis Induced by Anti-TNF Therapy in Patients with Inflammatory Bowel Disease: A Nationwide Cohort Study.炎症性肠病患者抗TNF治疗诱导的银屑病的发病率、临床特征及管理:一项全国性队列研究
Inflamm Bowel Dis. 2016 Apr;22(4):894-901. doi: 10.1097/MIB.0000000000000757.
8
Biological therapy increases the health-related quality of life in patients with inflammatory bowel disease in a clinical setting.在临床环境中,生物疗法可提高炎症性肠病患者与健康相关的生活质量。
Scand J Gastroenterol. 2016;51(6):706-11. doi: 10.3109/00365521.2015.1136352. Epub 2016 Jan 22.
9
An overview of developing TNF-α targeted therapy for the treatment of psoriasis.用于治疗银屑病的肿瘤坏死因子-α靶向治疗的进展概述。
Expert Opin Investig Drugs. 2015;24(10):1343-54. doi: 10.1517/13543784.2015.1076793. Epub 2015 Aug 8.
10
Cumulative incidence of, risk factors for, and outcome of dermatological complications of anti-TNF therapy in inflammatory bowel disease: a 14-year experience.炎症性肠病抗TNF治疗皮肤并发症的累积发病率、危险因素及转归:14年经验
Am J Gastroenterol. 2015 Aug;110(8):1186-96. doi: 10.1038/ajg.2015.205. Epub 2015 Jul 21.

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.

DOI:10.1002/acr.24100
PMID:31646743
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8176628/
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。