Parenchymal destruction in asthma: Fixed airflow obstruction and lung function trajectory

J Allergy Clin Immunol. 2022 Mar;149(3):934-942.e8. doi: 10.1016/j.jaci.2021.07.042. Epub 2021 Aug 24.

Abstract

Background: Fixed airflow obstruction (FAO) in asthma, particularly in nonsmokers, is generally believed to be caused by airway remodeling. However, parenchymal destruction may also contribute to FAO and longitudinal decline in forced expiratory volume in 1 second (FEV1).

Objectives: To evaluate parenchymal destruction, we used emphysema indices, exponent D, and low-attenuation area percentage (LAA%) on computed tomography (CT), and test whether the parenchymal destruction and airway disease are independently associated with FAO and FEV1 decline in both smoking and nonsmoking asthma.

Methods: Exponent D, LAA%, wall area percentage at segmental airways, and airway fractal dimension (AFD) in those with asthma were measured on inspiratory CT and compared to those in patients with chronic obstructive pulmonary disease (COPD).

Results: Exponent D was lower and LAA% was higher in COPD (n = 42) and asthma with FAO (n = 101) than in asthma without FAO (n = 88). The decreased exponent D and increased LAA% were associated with FAO regardless of smoking status or asthma severity. In multivariable analysis, decreased exponent D and increased LAA% were associated with an increased odds ratio of FAO and decreased FEV1, irrespective of wall area percentage and airway fractal dimension. Moreover, decreased exponent D affected the longitudinal decline in FEV1 in those with severe asthma, independent of smoking status.

Conclusions: Patients with asthma with FAO showed parenchymal destruction regardless of smoking status and asthma severity. Parenchymal destruction was associated with an accelerated FEV1 decline, suggesting the involvements of both airway and parenchyma in the pathophysiology of a subgroup of asthma.

Keywords: Asthma; computed tomography; fractal; low-attenuation area; nonsmokers; parenchyma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asthma*
  • Forced Expiratory Volume
  • Humans
  • Lung
  • Pulmonary Disease, Chronic Obstructive*
  • Pulmonary Emphysema* / diagnostic imaging