Risk of De Novo Inflammatory Bowel Disease in Patients With Psoriasis and Psoriatic Arthritis Treated With IL-17A Inhibitors: A Population-Based Study

IF 6.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Saqr Alsakarneh, Omar Al Ta’ani, Razan Aburumman, Inas Mikhail, Jana G. Hashash, Francis A. Farraye
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引用次数: 0

Abstract

IL-17 inhibitors effectively treat psoriasis and psoriatic arthritis but may increase the risk of inflammatory bowel disease (IBD). We assessed their association with IBD compared to apremilast. Utilising the TriNetX database, we analysed patients with psoriasis or ankylosing spondylitis initiating IL-17 inhibitors or apremilast. We used propensity score matching and Cox models to estimate IBD risk. Among 13,216 matched patients per group, 142 developed IBD with IL-17 inhibitors versus 60 with apremilast (aHR = 2.50, 95% CI: 1.85–3.39). IL-17 inhibitors increase IBD risk, necessitating careful patient selection and monitoring.

Abstract Image

IL-17A抑制剂治疗银屑病和银屑病关节炎患者新发炎症性肠病的风险:一项基于人群的研究
IL-17抑制剂有效治疗银屑病和银屑病关节炎,但可能增加炎症性肠病(IBD)的风险。我们评估了与阿普雷米司特相比,它们与IBD的关系。利用TriNetX数据库,我们分析了银屑病或强直性脊柱炎患者启动IL-17抑制剂或阿普米司特。我们使用倾向评分匹配和Cox模型来估计IBD风险。在每组13216例匹配的患者中,142例使用IL-17抑制剂,60例使用阿普米司特(aHR = 2.50, 95% CI: 1.85-3.39)。IL-17抑制剂增加IBD风险,需要仔细选择和监测患者。
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来源期刊
CiteScore
15.60
自引率
7.90%
发文量
527
审稿时长
3-6 weeks
期刊介绍: Alimentary Pharmacology & Therapeutics is a global pharmacology journal focused on the impact of drugs on the human gastrointestinal and hepato-biliary systems. It covers a diverse range of topics, often with immediate clinical relevance to its readership.
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