hla - b27相关疾病发生眼部和肠外表现的时间:免疫疗法的比较研究

IF 2.8 3区 医学 Q2 RHEUMATOLOGY
Negin Yavari, Karen M Wai, Amer F Alsoudi, Euna Koo, Chase A Ludwig, Andrea L Kossler, Quan Dong Nguyen, Prithvi Mruthyunjaya, Ehsan Rahimy
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引用次数: 0

摘要

目的:本研究比较了接受不同类型免疫治疗的人白细胞抗原(HLA)- b27相关疾病患者的眼肠外表现(O-EIMs)和眼肠外表现(EIMs)的发生率和事件发生时间。方法:采用2014年1月1日至2024年12月31日来自TriNetX网络的汇总电子健康记录进行回顾性队列研究。hla - b27相关疾病的患者如果在初始诊断时或之后新开了肿瘤坏死因子(TNF)、janus激酶(JAK)或白细胞介素(IL)抑制剂,则纳入。计算每100人年O-EIMs和EIMs的累积发病率。Kaplan-Meier估计使用R Studio(版本4.4.1)来绘制时间到事件结果的图表。结果:我们确定了22,287例患者[平均年龄47.2(16.8)岁;13132(58.9) %女性]。从指数日期起,葡萄膜炎的累积发病率为0.11例/ 100人年。根据首次用药,使用IL抑制剂的患者的前葡萄膜炎发病率最低,其次是JAK和TNF抑制剂(分别为0.07%,0.10%和0.20%,病例/ 100人年)。时间-事件分析显示,最初使用TNF抑制剂的患者发生前葡萄膜炎的可能性更高,尽管差异无统计学意义。对于EIMs,骶髂炎的发生率最高,TNF(0.91%),其次是JAK(0.72%)和IL(0.37%)。与TNF(2.19%)和IL(2.17%)相比,JAK抑制剂的银屑病皮炎发病率最高(2.85%)。结论:在hla - b27相关疾病患者的队列研究中,缺乏统计学意义表明不同免疫治疗类别在预防O-EIMs和EIMs方面的有效性相似。•使用TriNetX网络的真实数据,对接受TNF、JAK或IL抑制剂治疗的hla - b27相关疾病患者的O-EIMs和EIMs的发生时间进行大规模比较研究。•在所有免疫治疗类别中,观察到O-EIMs和EIMs的总发病率较低,在事件发生时间结果上没有统计学上的显著差异,表明预防这些表现的有效性相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time to incident ocular and extraintestinal manifestation in HLA-B27-Associated diseases: a comparative study of immunotherapies.

Objectives: This study compared the incidence and time-to-event outcomes of ocular extraintestinal manifestations (O-EIMs) and EIMs among patients with human leukocyte antigen (HLA)-B27-associated diseases receiving different classes of immunotherapy.

Methods: A retrospective cohort study was conducted using aggregated electronic health records from the TriNetX network between January 1, 2014, and December 31, 2024. Patients with HLA-B27-associated diseases were included if they were newly prescribed tumor necrosis factor (TNF), janus kinase (JAK), or interleukin (IL) inhibitors on or after their initial diagnosis. The cumulative incidence of O-EIMs and EIMs was calculated per 100 person-years. Kaplan-Meier estimates were used to graph time-to-event outcomes using R Studio (version 4.4.1).

Results: We identified 22,287 patients [mean age 47.2 (16.8) years; 13,132 (58.9) % women]. The cumulative incidence of anterior uveitis from the index date was 0.11 cases per 100 person-years. According to first medication prescribed, the incidence of anterior uveitis was lowest in patients prescribed IL inhibitors, followed by JAK and TNF inhibitors (0.07%, 0.10%, and 0.20%, cases per 100 person-years respectively). Time-to-event analysis showed a higher likelihood of anterior uveitis with initial TNF inhibitor use, although the difference was not statistically significant. Regarding EIMs, incident sacroiliitis was highest with TNF (0.91%), followed by JAK (0.72%) and IL (0.37%). Psoriatic dermatitis incidence was highest with JAK inhibitors (2.85%), compared to TNF (2.19%) and IL (2.17%).

Conclusion: In this cohort study of patients with HLA-B27-associated diseases, the lack of statistical significance indicates similar effectiveness across immunotherapy classes in preventing O-EIMs and EIMs. Key Points • Large-scale comparative study assessing time-to-incident O-EIMs and EIMs in patients with HLA-B27-associated diseases treated with TNF, JAK, or IL inhibitor therapies using real-world data from the TriNetX network. • Low overall incidence of O-EIMs and EIMs was observed across all immunotherapy classes, with no statistically significant difference in time-to-event outcomes, indicating similar effectiveness in preventing these manifestations.

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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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