Incidence of acne in patients with inflammatory bowel disease treated with Janus kinase inhibitors: a systematic review and meta-analysis.

IF 4.3 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Mohammed Nabil Quraishi, Maryam A Alahmad, Thaer Khaleel Swaid, Antonio Facciorusso, Alyssa A Grimshaw, Badr Al-Bawardy
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引用次数: 0

Abstract

Background: Janus kinase (JAK) inhibitors are effective oral therapies for inflammatory bowel disease (IBD). While acne is a known adverse event in dermatological cohorts, its incidence and risk factors in the IBD population are not well-defined. We aimed to determine the pooled incidence of acne in IBD patients treated with JAK inhibitors and to explore this risk across key clinical subgroups.

Methods: We conducted a systematic review and meta-analysis following PRISMA guidelines. MEDLINE, EMBASE, and CENTRAL were searched from inception to September 2025 for randomized controlled trials (RCTs) and observational studies reporting acne incidence in IBD patients on JAK inhibitors. Data were pooled using a random-effects generalized linear mixed-effects model. Pre-specified subgroup analyses were performed.

Results: A total of 50 studies (5 RCTs, 45 observational) involving 9902 IBD patients were included. The overall pooled incidence of acne was 8.6% (95% CI: 6.4%-11.6%). Acne rates were significantly higher (P < .0001) with the upadacitinib (12.2%), compared to tofacitinib (2.6%) and filgotinib (2.3%). A numerically higher incidence was observed during induction (8.6%) versus maintenance (4.2%) therapy, though this difference was not statistically significant (P = .07). The incidence was significantly higher in the pediatric population (12.2%) compared to adults (7.4%) (P = .03). In RCTs, JAK inhibitors were associated with significantly increased odds of acne compared to placebo (OR 2.43, 95% CI: 1.33-4.43, P = .019). No statistically significant difference was observed by IBD subtype.

Conclusion: Acne is a common adverse event in IBD patients treated with JAK inhibitors. The reported incidence of acne was significantly higher with upadacitinib, in the pediatric population, and numerically higher during the induction phase of treatment.

用Janus激酶抑制剂治疗炎症性肠病患者的痤疮发生率:一项系统回顾和荟萃分析
背景:Janus激酶(JAK)抑制剂是治疗炎症性肠病(IBD)的有效口服疗法。虽然痤疮在皮肤病人群中是一种已知的不良事件,但其在IBD人群中的发病率和危险因素尚不明确。我们的目的是确定接受JAK抑制剂治疗的IBD患者痤疮的总发生率,并在关键临床亚组中探讨这种风险。方法:我们按照PRISMA指南进行了系统回顾和荟萃分析。MEDLINE, EMBASE和CENTRAL检索了从成立到2025年9月的随机对照试验(rct)和观察性研究,报告了使用JAK抑制剂的IBD患者痤疮发生率。采用随机效应广义线性混合效应模型合并数据。进行预先指定的亚组分析。结果:共纳入50项研究(5项随机对照试验,45项观察性研究),涉及9902例IBD患者。痤疮的总合并发生率为8.6% (95% CI: 6.4%-11.6%)。与tofacitinib(2.6%)和filgotinib(2.3%)相比,upadacitinib(12.2%)的痤疮发生率显著高于(P < 0.0001)。诱导治疗(8.6%)与维持治疗(4.2%)的发生率较高,但差异无统计学意义(P = 0.07)。儿童人群的发病率(12.2%)明显高于成人(7.4%)(P = 0.03)。在随机对照试验中,与安慰剂相比,JAK抑制剂与痤疮发生率显著增加相关(OR 2.43, 95% CI: 1.33-4.43, P = 0.019)。不同IBD亚型间差异无统计学意义。结论:痤疮是使用JAK抑制剂治疗IBD患者常见的不良事件。据报道,在儿科人群中,upadacitinib的痤疮发生率明显更高,并且在治疗的诱导阶段数值更高。
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来源期刊
Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 医学-胃肠肝病学
CiteScore
9.70
自引率
6.10%
发文量
462
审稿时长
1 months
期刊介绍: Inflammatory Bowel Diseases® supports the mission of the Crohn''s & Colitis Foundation by bringing the most impactful and cutting edge clinical topics and research findings related to inflammatory bowel diseases to clinicians and researchers working in IBD and related fields. The Journal is committed to publishing on innovative topics that influence the future of clinical care, treatment, and research.
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