炎症性肠病诊断时的外周血嗜酸性粒细胞增多症与严重病程有关;一项来自 epi-IIRN 队列的全国性研究。

Anat Yerushalmy-Feler, Rona Lujan, Yiska Loewenberg Weisband, Shira Greenfeld, Amir Ben-Tov, Natan Ledderman, Eran Matz, Iris Dotan, Raffi Lev-Tzion, Idan Goren, Dan Turner, Shlomi Cohen
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引用次数: 0

摘要

背景与目的我们开展了这项全国性研究,以评估外周血嗜酸性粒细胞增多症(PBE)与儿童和成人炎症性肠病(IBD)患者长期预后之间的关系:方法: epi-IIRN 队列是一个经过验证的基于人群的 IBD 数据库,其数据包括 2005-2020 年间确诊的、在确诊时有嗜酸性粒细胞计数的患者以及非 IBD 对照组患者的数据。嗜酸性粒细胞计数>0.5 X109/L定义为PBE。严重病程定义为依赖皮质类固醇、使用≥2种不同类别的生物制剂或手术。包括严重病程在内的转归时间由 Cox 比例危险模型确定:共纳入 28,133 名患者(15,943 名克罗恩病 [CD] 患者和 12,190 名溃疡性结肠炎 [UC] 患者)和 28,724 名非克罗恩病对照组患者。IBD 组 PBE 患病率为 13%,对照组为 5%(P < .001)。与 CD(10.6%,OR=1.52 (95%CI 1.42-1.63);P < .001)相比,PBE 在 UC(16.1%)中的发病率更高;与成人 IBD(11%)相比,PBE 在儿童 IBD(23.5%)中的发病率更高(OR=2.14 (1.97-2.31);P 结论:在这项最大规模的全国性研究中,PBE可预测严重的IBD病程。这些发现支持将 PBE 作为 IBD 不良结局的标志物,并作为未来疗法的潜在靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Peripheral Blood Eosinophilia at Diagnosis of Inflammatory Bowel Disease Is Associated with Severe Disease Course; A Nationwide Study From the epi-IIRN Cohort.

Background & aims: We conducted this nationwide study to evaluate the association between peripheral blood eosinophilia (PBE) and long-term outcomes in children and adults with inflammatory bowel diseases (IBD).

Methods: Data from the epi-IIRN cohort, a validated population-based IBD database, included patients diagnosed between 2005-2020 who had an eosinophil count at diagnosis, and those of non-IBD controls. PBE was defined as an eosinophil count of >0.5 X109/L Severe disease course was defined as corticosteroid dependency, use of ≥2 biologics from different classes, or surgery. Time-to-outcomes, including severe disease course, was determined by Cox proportional hazard models.

Results: Included were 28,133 patients (15,943 Crohn's disease [CD] and 12,190 ulcerative colitis [UC]), and 28,724 non-IBD controls. The prevalence of PBE was 13% in the IBD group and 5% in controls (P < .001). PBE was more prevalent in UC (16.1%) compared to CD (10.6%, OR=1.52 (95%CI 1.42-1.63); P < .001) and in pediatric-onset (23.5%) compared to adult-onset (11%) IBD (OR=2.14 (1.97-2.31); P <.001). In a multivariate analysis, PBE was a predictor of severe disease course in IBD (hazard ratio [HR]=1.49, 95%CI 1.38-1.62, P < .001). PBE also predicted time-to-hospitalization (HR=1.24, 95%CI 1.19-1.30), use of corticosteroids (HR=1.32, 95%CI 1.28-1.36), corticosteroid dependency (HR=1.37, 95%CI 1.31-1.43), and need of biologics (HR=1.27, 95%CI 1.21-1.33).

Conclusion: In this largest nationwide study, PBE predicted severe IBD course. These findings support the use of PBE as a marker of adverse outcome of IBD and as a potential target for future therapies.

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