AI Article Synopsis

  • Blood eosinophil count (BEC) is used for evaluating T2 inflammation in severe asthma, but its connection to tissue changes remains unclear; bronchial biopsy may clarify this issue with a standardized pathological scoring system.
  • A systematic evaluation of various tissue characteristics (like eosinophilic count and goblet cell hyperplasia) was conducted on biopsies from severe uncontrolled asthma patients, showing strong agreement among pathologists and significant correlations between BEC, tissue eosinophil count (TEC), and fractional exhaled nitric oxide (FeNO).
  • The study concludes that a standardized assessment of bronchial biopsy can enhance the understanding and classification of severe uncontrolled asthma, especially in patients undergoing treatment with oral corticosteroids.

Article Abstract

Background: Blood eosinophil count (BEC) is currently used as a surrogate marker of T2 inflammation in severe asthma but its relationship with tissue T2-related changes is elusive. Bronchial biopsy could add reliable information but lacks standardization.

Objectives: To validate a systematic assessment of the bronchial biopsy for the evaluation of severe uncontrolled asthma (SUA) by standardizing a pathological score.

Methods: A systematic assessment of submucosal inflammation, tissue eosinophilic count/field (TEC), goblet cells hyperplasia, epithelial changes, basement membrane thickening, prominent airway smooth muscle and submucosal mucous glands was initially agreed and validated in representative bronchial biopsies of 12 patients with SUA by 8 independent pathologists. In a second phase, 62 patients with SUA who were divided according to BEC≥300cells/mm or less underwent bronchoscopy with bronchial biopsies and the correlations between the pathological findings and the clinical characteristics were investigated.

Results: The score yielded good agreement among pathologists regarding submucosal eosinophilia, TEC, goblet cells hyperplasia and mucosal glands (ICC=0.85, 0.81, 0.85 and 0.87 respectively). There was a statistically significant correlation between BEC and TEC (r=0.393, p=0.005) that disappeared after correction by oral corticosteroids (OCS) use (r=0.170, p=0.307). However, there was statistically significant correlation between FeNO and TEC (r=0.481, p=0.006) that was maintained after correction to OCS use (r=0.419, p=0.021). 82.4% of low-BEC had submucosal eosinophilia, 50% of them moderate to severe.

Conclusion: A standardized assessment of endobronchial biopsy is feasible and could be useful for a better phenotyping of SUA especially in those receiving OCS.

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Source
http://dx.doi.org/10.1016/j.arbres.2023.05.014DOI Listing

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