CCAD or eCRS: Defining Eosinophilic Subpopulations in Chronic Rhinosinusitis

被引:7
|
作者
Sit, Andrea [1 ,2 ]
Alvarado, Raquel [1 ]
Earls, Peter [1 ,3 ]
Rimmer, Janet [1 ,4 ,5 ]
Kalish, Larry [1 ,6 ,7 ]
Campbell, Raewyn [1 ,8 ,9 ]
Sewell, William [2 ,10 ]
Harvey, Richard J. [1 ,9 ]
机构
[1] St Vincents Ctr Appl Med Res, Rhinol & Skull Base Res Grp, 67 Burton St, Sydney, NSW 2010, Australia
[2] Univ New South Wales, St Vincents Clin Sch, Sydney, NSW, Australia
[3] St Vincents Hosp, Dept Anat Pathol, Sydney, NSW, Australia
[4] Univ Sydney, Woolcock Inst, Sydney, NSW, Australia
[5] Notre Dame Univ, Fac Med, Sydney, NSW, Australia
[6] Univ Sydney, Fac Med, Sydney, NSW, Australia
[7] Concord Gen Hosp, Dept Otolaryngol Head & Neck Surg, Sydney, NSW, Australia
[8] Royal Prince Alfred Hosp, Dept Otolaryngol Head & Neck Surg, Sydney, NSW, Australia
[9] Macquarie Univ, Fac Med Hlth & Human Sci, Sydney, NSW, Australia
[10] Garvan Inst, Immunol Div, Sydney, NSW, Australia
关键词
chronic rhinosinusitis; eosinophils; CCAD; middle turbinate oedema; polyps; allergy; allergic rhinitis; phenotype; endotype; type; 2; Th2; central compartment; inhalant allergy; NASAL POLYPS; HISTOPATHOLOGY; PEROXIDASE; EOTAXIN-3; MARKERS;
D O I
10.1177/19458924231155012
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background Central compartment atopic disease (CCAD) and eosinophilic chronic rhinosinusitis (eCRS) are two clinical phenotypes of primary diffuse type 2 chronic rhinosinusitis (CRS) defined in the European Position Paper on Rhinosinusitis 2020 classification. Currently, the distinction between these subtypes relies on phenotypic features alone. Objective This study aimed to investigate whether eosinophil activation differed between CCAD and eCRS. Methods A cross-sectional study was conducted of adult patients presenting with CCAD and eCRS who had undergone functional endoscopic sinus surgery. Routine pathology results were obtained from clinical records. Eosinophils were counted on haematoxylin and eosin-stained formalin-fixed paraffin-embedded sinonasal tissue. Eotaxin-3, eosinophil peroxidase and immunoglobulin E levels were assessed using immunohistochemistry. Results 38 participants were included (51.7 +/- 15.6 years, 47.4% female), of whom 36.8% were diagnosed with CCAD and 63.2% with eCRS. The eCRS group was characterised by older age (55.8 +/- 16.3 vs 44.5 +/- 11.8 years, p = 0.029), and on histology exhibited a higher degree of tissue inflammation (tau(b) = 0.409, p = 0.011), greater proportion of patients with >100 eosinophils/high power field (87.5% vs 50%, p = 0.011), and higher absolute tissue eosinophil count (2141 +/- 1947 vs 746 +/- 519 cells/mm(2), p = 0.013). Eotaxin-3 scores were higher in the eCRS group (5.00[5.00-6.00] vs 6.00[6.00-6.75], p = 0.015). Other outcomes were similar. Conclusions Eosinophil and eotaxin-3 levels were elevated in eCRS compared with CCAD, suggesting a greater degree of eosinophil stimulation and chemotaxis. Patients with CCAD were younger. Future investigation and biomarkers may better distinguish CRS subpopulations.
引用
收藏
页码:402 / 409
页数:8
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