Long‐term clinical outcomes of aspirin‐exacerbated respiratory disease: Real‐world data from an adult asthma cohort

Author:

Lee Youngsoo1ORCID,Kim Chungsoo2ORCID,Lee Eunyoung34ORCID,Lee Hyun Young5ORCID,Woo Seong‐Dae6ORCID,You Seng Chan7ORCID,Park Rae Woong23ORCID,Park Hae‐Sim1ORCID

Affiliation:

1. Department of Allergy & Clinical Immunology Ajou University School of Medicine Suwon South Korea

2. Department of Biomedical Sciences Ajou University Graduate School of Medicine Suwon South Korea

3. Department of Biomedical Informatics Ajou University School of Medicine Suwon South Korea

4. Office of Biostatistics, Ajou Research Institute for Innovative Medicine Ajou University Medical Center Suwon South Korea

5. Department of Statistics, Clinical Trial Center Ajou University Medical Center Suwon South Korea

6. Division of Pulmonology and Allergy Chungnam National University School of Medicine Daejeon South Korea

7. Department of Biomedicine System Informatics Yonsei University College of Medicine Seoul South Korea

Abstract

AbstractBackgroundAspirin‐exacerbated respiratory disease (AERD) is a phenotype of severe asthma, but its disease course has not been well documented compared with that of aspirin‐tolerant asthma (ATA).ObjectivesThis study aimed to investigate the long‐term clinical outcomes between AERD and ATA.MethodsAERD patients were identified by the diagnostic code and positive bronchoprovocation test in a real‐world database. Longitudinal changes in lung function, blood eosinophil/neutrophil counts, and annual numbers of severe asthma exacerbations (AEx) were compared between the AERD and the ATA groups. Within a year after baseline, two or more severe AEx events indicated severe AERD, whereas less than two AEx events indicated nonsevere AERD.ResultsAmong asthmatics, 353 had AERD in which 166 and 187 patients had severe and nonsevere AERD, respectively, and 717 had ATA. AERD patients had significantly lower FEV1%, higher blood neutrophil counts, and higher sputum eosinophils (%) (all p < .05) as well as higher levels of urinary LTE4 and serum periostin, and lower levels of serum myeloperoxidase and surfactant protein D (all p < .01) than those with ATA. In a 10‐year follow‐up, the severe AERD group maintained lower FEV1% with more severe AEs than the nonsevere AERD group.Conclusion and Clinical RelevanceWe demonstrated that AERD patients presented poorer long‐term clinical outcomes than ATA patients in real‐world data analyses.

Funder

Korea Health Industry Development Institute

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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