The Incidence and Management of TNF-α Inhibitor Induced Paradoxical Psoriasis in Children With Inflammatory Bowel Disease: A Systematic Review and Meta-Analysis.

IF 1.8 4区 医学 Q2 DERMATOLOGY
Australasian Journal of Dermatology Pub Date : 2025-08-01 Epub Date: 2025-05-21 DOI:10.1111/ajd.14526
James Gaston, Tai Ermongkonchai, Andrew Chen, Senhong Lee, Francis Yi Xing Lai
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引用次数: 0

Abstract

Paradoxical psoriasis is a well-described phenomenon following treatment with Tumour Necrosis Factor alpha (TNF-α) inhibitors in adult patients with Inflammatory Bowel Disease (IBD). The incidence and optimal treatment strategies are not well described in children with IBD. This subgroup of patients is disproportionately impacted by TNF-α inhibitor-induced psoriatic eruptions. Our systematic review and meta-analyses aims to describe the incidence, presentation, and management options for TNF-αinhibitor-induced psoriasis in paediatric patients with IBD. A systematic literature search was conducted using Medline, Embase and Cochrane databases for studies published up to February 2025. Retrospective cohort studies (n = 16), prospective cohort study (n = 1), and a cross-sectional study (n = 1) met inclusion criteria. Studies focusing on patients > 18 years or TNF-α inhibitors used for non-IBD conditions were excluded. A total of 3349 paediatric patients with IBD treated with TNF-α inhibitors were analysed, with 255 (7.6%) developing paradoxical psoriasis. Meta-analysis of 13 studies meeting sample size criteria yielded a pooled incidence of 6.8% (95% CI: 0.04-0.10). Infliximab (IFX) accounted for 151 (79.1%) of cases, whereas adalimumab (ADA) contributed to 40 (20.9%) cases. The median time to clinical eruption was 15.0 months (12.0-18.0). Among affected patients, 22.3% (51/229) discontinued their prescribed TNF-α inhibitor and 5.7% (13/229) were subsequently switched to an alternative TNF-α inhibitor. Ustekinumab (UST) was the most common non-TNF-α alternative (14/94). TNF-α inhibitor-induced psoriasis is a common adverse effect in paediatric IBD, with a significant proportion of cases necessitating treatment discontinuation. Long-term outcomes following a switch to non-TNF-α biologics remain unclear, highlighting the need for further prospective studies.

炎症性肠病患儿TNF-α抑制剂诱导的矛盾型牛皮癣的发病率和治疗:系统回顾和荟萃分析
悖论型牛皮癣是炎症性肠病(IBD)成人患者在接受肿瘤坏死因子α (TNF-α)抑制剂治疗后出现的一种很好的现象。儿童IBD的发病率和最佳治疗策略尚未得到很好的描述。该亚组患者不成比例地受到TNF-α抑制剂诱导的银屑病爆发的影响。我们的系统综述和荟萃分析旨在描述儿童IBD患者中TNF-α抑制剂诱导的牛皮癣的发病率、表现和管理选择。使用Medline、Embase和Cochrane数据库对截至2025年2月发表的研究进行了系统的文献检索。回顾性队列研究(n = 16)、前瞻性队列研究(n = 1)和横断面研究(n = 1)符合纳入标准。排除了针对bb0 ~ 18岁患者或用于非ibd的TNF-α抑制剂的研究。研究共分析了3349例接受TNF-α抑制剂治疗的IBD患儿,其中255例(7.6%)发展为异型牛皮癣。对13项符合样本量标准的研究进行荟萃分析,总发病率为6.8% (95% CI: 0.04-0.10)。英夫利昔单抗(IFX)占151例(79.1%),而阿达木单抗(ADA)占40例(20.9%)。到临床出疹的中位时间为15.0个月(12.0 ~ 18.0个月)。在受影响的患者中,22.3%(51/229)停用了他们的处方TNF-α抑制剂,5.7%(13/229)随后切换到替代TNF-α抑制剂。Ustekinumab (UST)是最常见的非tnf -α替代方案(14/94)。TNF-α抑制剂诱导的牛皮癣是儿科IBD常见的不良反应,有相当大比例的病例需要停药。改用非tnf -α生物制剂后的长期结果尚不清楚,因此需要进一步的前瞻性研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.20
自引率
5.00%
发文量
186
审稿时长
6-12 weeks
期刊介绍: Australasian Journal of Dermatology is the official journal of the Australasian College of Dermatologists and the New Zealand Dermatological Society, publishing peer-reviewed, original research articles, reviews and case reports dealing with all aspects of clinical practice and research in dermatology. Clinical presentations, medical and physical therapies and investigations, including dermatopathology and mycology, are covered. Short articles may be published under the headings ‘Signs, Syndromes and Diagnoses’, ‘Dermatopathology Presentation’, ‘Vignettes in Contact Dermatology’, ‘Surgery Corner’ or ‘Letters to the Editor’.
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