Szczegóły publikacji

Opis bibliograficzny

Non-eosinophilic asthma in nonsteroidal anti-inflammatory drug exacerbated respiratory disease / Lucyna Mastalerz, Natalia Celejewska-Wójcik, Adam ĆMIEL, Krzysztof Wójcik, Joanna Szaleniec, Karolina Hydzik-Sobocińska, Jerzy Tomik, Marek Sanak // Clinical and Translational Allergy [Dokument elektroniczny]. — Czasopismo elektroniczne ; ISSN 2045-7022. — 2023 — vol. 13 iss. 3 art. no. e12235, s. 1–9. — Wymagania systemowe: Adobe Reader. — Bibliogr. s. 8–9, Abstr. — Publikacja dostępna online od: 2023-03-13

Autorzy (8)

  • Mastalerz Lucyna
  • Celejewska-Wójcik Natalia
  • AGHĆmiel Adam
  • Wójcik Krzysztof t
  • Szaleniec Joanna
  • Hydzik-Sobocińska Karolina
  • Tomik Jerzy
  • Sanak Marek

Słowa kluczowe

aspirin hypersensitivityinflammatory phenotypescluster analysisnon eosinophilic asthma

Dane bibliometryczne

ID BaDAP150049
Data dodania do BaDAP2023-12-05
Tekst źródłowyURL
DOI10.1002/clt2.12235
Rok publikacji2023
Typ publikacjiartykuł w czasopiśmie
Otwarty dostęptak
Creative Commons
Czasopismo/seriaClinical and Translational Allergy

Abstract

Background: The cellular inflammatory pattern of nonsteroidal anti-inflammatory drug–exacerbated respiratory disease (N-ERD) is heterogeneous. However, data on the heterogeneity of non-eosinophilic asthma (NEA) with aspirin hypersensitivity are scanty. By examination of N-ERD patients based on clinical data and eicosanoid biomarkers we aimed to identify NEA endotypes potentially guiding clinical management. Methods: Induced sputum was collected from patients with N-ERD. Sixty six patients (49.6% of 133 N-ERD) with NEA were included in the hierarchical cluster analysis based on clinical and laboratory data. The quality of clustering was evaluated using internal cluster validation with different indices and a practical decision tree was proposed to simplify stratification of patients. Results: The most frequent NEA pattern was paucigranulocytic (PGA; 75.8%), remaining was neutrophilic asthma (NA; 24.2%). Four clusters were identified. Cluster #3 included the highest number of NEA patients (37.9%) with severe asthma and PGA pattern (96.0%). Cluster #1 (24.2%) included severe only asthma, with a higher prevalence of NA (50%). Cluster #2 (25.8%) comprised well-controlled mild or severe asthma (PGA; 76.5%). Cluster #4 contained only 12.1% patients with well-controlled moderate asthma (PGA; 62.5%). Sputum prostaglandin D2 levels distinguished cluster #1 from the remaining clusters with an area under the curve of 0.94. Conclusions: Among identified four NEA subtypes, clusters #3 and #1 represented N-ERD patients with severe asthma but a different inflammatory signatures. All the clusters were discriminated by sputum PGD2 levels, asthma severity, and age of patients. The heterogeneity of non-eosinophilic N-ERD suggests a need for novel targeted interventions. © 2023 The Authors. Clinical and Translational Allergy published by John Wiley & Sons Ltd on behalf of European Academy of Allergy and Clinical Immunology.

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