Eosinophilic Esophagitis as a Complex Th2 Inflammatory Disease: Results of a Prospective Long-Term Study in Children.

IF 2.1
Digestive diseases (Basel, Switzerland) Pub Date : 2026-01-01 Epub Date: 2025-11-07 DOI:10.1159/000549092
Sabrina Degen, Theresa Hironimus, Tobias Rechenauer, Christoph Ehrsam, Anja Rabe, Adrian Regensburger, Aline Rückel, Arndt Hartmann, Ralf Rieker, Joachim Woelfle, Anja Rappl, André Hoerning
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引用次数: 0

Abstract

Introduction: While the eosinophilic esophagitis (EoE) has become the second most common disease entity causing esophageal dysfunction, there is currently a lack of data reporting on pediatric EoE from Germany. This monocentric longitudinal study seeks to fill this gap by investigating treatment success, atopic co-morbidities, and potential blood parameters in a real-world setting.

Methods: This study analyzed data on children with EoE (n = 50), gastroesophageal reflux disease (GERD, n = 13), and controls (n = 5). Evaluated characteristics included clinical manifestations, atopy, and treatment success during disease progress. We defined the primary endpoint as histological remission in all esophageal locations (proximal, mid, distal). Secondary endpoints were histological-clinical, histological-endoscopic, and histological-clinical-endoscopic remission.

Results: Of 50 patients (0.5-16.9 years), 26% (n = 13) responded to proton-pump inhibitors (PPI-R) and 74% (n = 37) needed other forms of treatment (PPI-NR). Atopic co-morbidities were observed in 46% (PPI-NR) and 23% (PPI-R). Primary PPI treatment resulted in histological remission in 13 patients (median: 2 [2;4.5] months); only one (8%) achieved complete endoscopic-clinical-histological remission. Thirty-two PPI-NRs (84%) reached histological remission after a median of 7 [4;11] months, but only eleven (34%) acquired complete histological-clinical-endoscopic remission. Absolute blood eosinophil count (AEC) was increased within active EoE (420 [250;550] cells/µL). It distinguished EoE from controls (cutoff 90 cells/µL, sensitivity/specificity: 95.7%/80%) and from GERD (180 cells/µL, 87.5%/66.7%). Eosinophilic cationic protein (ECP) differed between children with active EoE and controls (10 µg/L, 86.7%/100%).

Conclusions: Patients' characteristics are comparable to those from other European countries. AEC and ECP were increased in EoE patients. Achieving complete remission required an intensified therapy regime.

.

嗜酸性粒细胞性食管炎是一种复杂的Th2炎症性疾病:一项儿童前瞻性长期研究的结果
虽然嗜酸性粒细胞性食管炎(EoE)已成为导致食管功能障碍的第二大常见疾病,但目前缺乏德国儿童EoE的数据报道。这项单中心纵向研究试图通过调查治疗成功、特应性合并症和现实世界中潜在的血液参数来填补这一空白。方法:本研究分析了EoE患儿(n=50)、胃食管反流病患儿(n= 13)和对照组(n=5)的资料。评估的特征包括临床表现、疾病进展期间的特应性和治疗成功。我们将主要终点定义为所有食管部位(近端、中端、远端)的组织学缓解。次要终点是组织-临床、组织-内窥镜和组织-临床-内窥镜缓解。结果:50例患者(0.5-16.9岁)中,26% (n=13)对质子泵抑制剂(PPI-R)有反应,74% (n=37)需要其他形式的治疗(PPI-NR)。46% (PPI-NR)和23% (PPI-R)观察到特应性合并症。初级PPI治疗导致13例患者的组织学缓解(中位数:2[2;4.5]个月),只有1例(8%)实现了完全的内镜-临床-组织学缓解。32例PPI-NR(84%)达到组织学缓解,中位数为7 [4];11个月,但只有11例(34%)获得了完全的组织学-临床-内镜缓解。活性EoE内绝对血嗜酸性粒细胞计数(AEC)升高(420[250;550]个细胞/µL)。它将EoE与对照组(截止值为90个细胞/µL,灵敏度/特异性:95.7%/80%)和GERD(180个细胞/µL, 87.5%/66.7%)区分开来。活性EoE患儿的嗜酸性阳离子蛋白(ECP)与对照组差异较大(10µg/L, 86.7%/100%)。结论:患者的特征与其他欧洲国家的患者具有可比性。EoE患者AEC和ECP升高。达到完全缓解需要强化治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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