Respiratory Research (Oct 2023)

Bronchial epithelial gene expression and interstitial lung abnormalities

  • Aravind A. Menon,
  • Minyi Lee,
  • Xu Ke,
  • Rachel K. Putman,
  • Takuya Hino,
  • Jonathan A. Rose,
  • Fenghai Duan,
  • Samuel Y. Ash,
  • Michael H. Cho,
  • George T. O’Connor,
  • Josée Dupuis,
  • Hiroto Hatabu,
  • Marc E. Lenburg,
  • Ehab S. Billatos,
  • Gary M. Hunninghake,
  • the DECAMP Investigators

DOI
https://doi.org/10.1186/s12931-023-02536-w
Journal volume & issue
Vol. 24, no. 1
pp. 1 – 7

Abstract

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Abstract Introduction Interstitial lung abnormalities (ILA) often represent early fibrotic changes that can portend a progressive fibrotic phenotype. In particular, the fibrotic subtype of ILA is associated with increased mortality and rapid decline in lung function. Understanding the differential gene expression that occurs in the lungs of participants with fibrotic ILA may provide insight into development of a useful biomarker for early detection and therapeutic targets for progressive pulmonary fibrosis. Methods Measures of ILA and gene expression data were available in 213 participants in the Detection of Early Lung Cancer Among Military Personnel (DECAMP1 and DECAMP2) cohorts. ILA was defined using Fleischner Society guidelines and determined by sequential reading of computed tomography (CT) scans. Primary analysis focused on comparing gene expression in ILA with usual interstitial pneumonia (UIP) pattern with those with no ILA. Results ILA was present in 51 (24%) participants, of which 16 (7%) were subtyped as ILA with a UIP pattern. One gene, pro platelet basic protein (PPBP) and seventeen pathways (e.g. TNF-α signalling) were significantly differentially expressed between those with a probable or definite UIP pattern of ILA compared to those without ILA. 16 of these 17 pathways, but no individual gene, met significance when comparing those with ILA to those without ILA. Conclusion Our study demonstrates that abnormal inflammatory processes are apparent in the bronchial airway gene expression profiles of smokers with and without lung cancer with ILA. Future studies with larger and more diverse populations will be needed to confirm these findings.

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