Piao Yurong, Xu Xiaolin, Yao Xingfeng, Li Yan, Sun Yixin, Han Tongxin, Wang Xiaoling, Mao Huawei
Department of Immunology, Beijing Children's Hospital, National Center for Children's Health, Capital Medical University, Beijing, China.
Department of Pharmacy, Beijing Children's Hospital, National Center for Children's Health, Capital Medical University, Beijing, China.
Pediatr Res. 2025 Jul 23. doi: 10.1038/s41390-025-04305-5.
Paradoxical psoriasis (PP) is a class of adverse events associated with tumor necrosis factor α inhibitor (TNFi) that are realistically observed in the real world. We aim to quantify the signals of PP with TNFis in pediatric patients based on a pharmacovigilance study.
Data on pediatric PP cases linked to five TNFi drugs-etanercept, infliximab, adalimumab, certolizumab, and golimumab-were extracted from the FDA Adverse Event Reporting System (FAERS) database (Q1 2004 to Q1 2023). PP event reports were assessed using ROR, PRR, BCPNN, MGPS, and logistic regression to conduct a disproportionality analysis and identify signal disparities.
The FAERS database noted 563 pediatric PP cases, with 33.69% male and 66.31% female, representing 0.58% of all pediatric TNFi adverse event reports. The average age was 14 years. Among the five TNFis, four showed disproportionate reporting of PP: etanercept [ROR = 18.53], infliximab [ROR = 17.19], adalimumab [ROR = 10.23], and certolizumab [ROR = 3.95].
The real-world FAERS pharmacovigilance data showed the safety signal for PP associated with TNFi in pediatric patients. Etanercept, infliximab, adalimumab, and certolizumab showed disproportionate reporting.
This study collected and analysed the data of paradoxical psoriasis (PP) associated with TNFis in pediatric patients from a worldwide pharmacovigilance database. Reports of PP adverse events accounted for 0.58% of the overall TNFi adverse event reports in pediatric patients. Among the five TNFis, we found disproportionate reporting of PP with etanercept, infliximab, adalimumab, and certolizumab in pediatric patients.
反常性银屑病(PP)是一类与肿瘤坏死因子α抑制剂(TNFi)相关的不良事件,在现实世界中确实可以观察到。我们旨在通过一项药物警戒研究来量化儿科患者中TNFi引发PP的信号。
从美国食品药品监督管理局不良事件报告系统(FAERS)数据库(2004年第一季度至2023年第一季度)中提取与五种TNFi药物(依那西普、英夫利昔单抗、阿达木单抗、赛妥珠单抗和戈利木单抗)相关的儿科PP病例数据。使用报告比值比(ROR)、比例报告比值(PRR)、贝叶斯置信传播神经网络(BCPNN)、多伽马泊松收缩法(MGPS)和逻辑回归对PP事件报告进行评估,以进行不成比例分析并识别信号差异。
FAERS数据库记录了563例儿科PP病例,其中男性占33.69%,女性占66.31%,占所有儿科TNFi不良事件报告的0.58%。平均年龄为14岁。在这五种TNFi中,有四种显示出PP报告不成比例:依那西普[ROR = 18.53]、英夫利昔单抗[ROR = 17.19]、阿达木单抗[ROR = 10.23]和赛妥珠单抗[ROR = 3.95]。
现实世界的FAERS药物警戒数据显示了儿科患者中与TNFi相关的PP的安全信号。依那西普、英夫利昔单抗、阿达木单抗和赛妥珠单抗显示出报告不成比例。
本研究从全球药物警戒数据库中收集并分析了儿科患者中与TNFi相关的反常性银屑病(PP)的数据。PP不良事件报告占儿科患者总体TNFi不良事件报告的0.58%。在这五种TNFi中,我们发现儿科患者中依那西普、英夫利昔单抗、阿达木单抗和赛妥珠单抗的PP报告不成比例。