基于2型炎症标志物的慢性鼻窦炎患者特征:来自欧洲CRS结局登记(CHRINOSOR)的发现

IF 4 2区 医学 Q2 ALLERGY
Carlo Cavaliere, Sven F. Seys, Joost de Kinderen, Giulia Bettio, Alexandros Andrianakis, Isam Alobid, Peter W. Hellings, Laura Van Gerven, Valérie Hox, Claire Hopkins, Anette Kjeldsen, Sietze Reitsma, Sven Schneider, Peter-Valentin Tomazic, Zuzana Diamant, Julia Eckl-Dorna, Wytske J. Fokkens, Clemens Holzmeister, Kenneth Larsen, Anu Laulajainen-Hongisto, Antonella Loperfido, Valerie Lund, Gert Mariën, Simonetta Masieri, Geoffrey Mortuaire, Mathilde Moyaert, Joaquim Mullol, Josje Otten, Camilo Rodriquez-Van Strahlen, Martin Wagenmann, Claus Bachert
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引用次数: 0

摘要

背景原发性慢性鼻窦炎(CRS)可根据受累的鼻窦和粘膜炎症的主要内型进行分类。自从引入2型靶向生物制剂作为CRS的治疗选择以来,炎症状态的评估在CRS患者中变得越来越重要。我们在这里的目的是表征伴有和不伴有2型炎症标志物升高的CRS患者。方法邀请在欧洲7个国家的10个三级中心之一的门诊就诊的CRS患者使用Galenus Health移动应用程序对其疾病进行监测。结果281例CRS患者按血嗜酸性粒细胞计数或BEC (<; 150细胞/μL: 21.6%,≥150细胞/μL: 78.4%; <; 250细胞/μL: 36.3%,≥250细胞/μL: 63.7%)和血清总IgE (< 100 IU/mL: 59.9%,≥100 IU/mL: 40.1%)分层。BEC与血清总IgE相关性不佳(Spearman r = 0.06; p = 0.39)。与BEC低于150或250 cells/μL的CRS患者相比,BEC≥150或250 cells/μL的CRS患者在总CRS症状、嗅觉丧失、鼻塞、流鼻涕方面的NPS、SNOT-22、VAS均增加。血清总IgE升高(≥100 IU/mL)的CRS患者与低于100 IU/mL的患者相比,结果参数没有差异。伴有哮喘的CRS患者(58.9%)与无哮喘患者相比,SNOT-22和VAS嗅觉丧失增加。结论:相当比例的CRS患者表现为2型内型,其特征为血嗜酸性粒细胞增多(78%),血清总IgE升高(40%)和/或合并哮喘(59%)。我们的研究结果强调了嗜酸性粒细胞作为2型炎症和严重程度标记物的有效性,但挑战了血清总IgE的实用性,因为它与任何严重程度标记物都不相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Characterization of Chronic Rhinosinusitis Patients Based on Markers of Type 2 Inflammation: Findings From the European CRS Outcome Registry (CHRINOSOR)

Characterization of Chronic Rhinosinusitis Patients Based on Markers of Type 2 Inflammation: Findings From the European CRS Outcome Registry (CHRINOSOR)

Background

Primary chronic rhinosinusitis (CRS) can be classified based on the sinuses involved and the dominant endotype of the mucosal inflammation. Since the introduction of type 2 targeted biologics as treatment option for CRS, assessment of the inflammatory status has gained importance in CRS patients. We here aimed to characterize CRS patients with and without elevated markers of type 2 inflammation.

Methods

CRS patients who visited the outpatient ENT clinic in one of the 10 tertiary centers in 7 European countries were invited to use the Galenus Health mobile application for the monitoring of their disease.

Results

CRS patients (n = 281) were stratified according to blood eosinophil counts or BEC (< 150 cells/μL: 21.6% of patients, ≥ 150 cells/μL: 78.4%; < 250 cells/μL: 36.3%, ≥ 250 cells/μL: 63.7%) and serum total IgE (< 100 IU/mL: 59.9%, ≥ 100 IU/mL: 40.1%). BEC and serum total IgE did not correlate well (Spearman r = 0.06; p = 0.39). CRS patients with BEC ≥ 150 cell/μL or ≥ 250 cells/μL, respectively, showed increased NPS, SNOT-22, VAS for total CRS symptoms, loss of smell, nasal blockage, runny nose compared to patients with BEC below 150 or 250 cells/μL. CRS patients with increased serum total IgE (≥ 100 IU/mL) did not show differences in the outcome parameters compared to patients with levels below 100 IU/mL. CRS patients with asthma (58.9%) showed increased SNOT-22 and VAS loss of smell compared to patients without asthma.

Conclusions

A significant proportion of CRS patients exhibit a type 2 endotype, characterized by blood eosinophilia (78%), increased serum total IgE (40%) and/or concomitant asthma (59%). Our results underline the usefulness of eosinophils as a marker of type 2 inflammation and severity but challenge the utility of serum total IgE since it does not correlate with any of the markers of severity.

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来源期刊
Clinical and Translational Allergy
Clinical and Translational Allergy Immunology and Microbiology-Immunology
CiteScore
7.50
自引率
4.50%
发文量
117
审稿时长
12 weeks
期刊介绍: Clinical and Translational Allergy, one of several journals in the portfolio of the European Academy of Allergy and Clinical Immunology, provides a platform for the dissemination of allergy research and reviews, as well as EAACI position papers, task force reports and guidelines, amongst an international scientific audience. Clinical and Translational Allergy accepts clinical and translational research in the following areas and other related topics: asthma, rhinitis, rhinosinusitis, drug hypersensitivity, allergic conjunctivitis, allergic skin diseases, atopic eczema, urticaria, angioedema, venom hypersensitivity, anaphylaxis, food allergy, immunotherapy, immune modulators and biologics, animal models of allergic disease, immune mechanisms, or any other topic related to allergic disease.
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