4.7 Article

Latent traits of lung tissue patterns in former smokers derived by dual channel deep learning in computed tomography images

期刊

SCIENTIFIC REPORTS
卷 11, 期 1, 页码 -

出版社

NATURE PORTFOLIO
DOI: 10.1038/s41598-021-84547-5

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资金

  1. NIH [U01-HL114494, R01-HL130506, R01-HL112986, S10-RR022421, S10-OD018526, T32-HL144461]
  2. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2017R1D1A1A09082160]
  3. Korea Environment Industry and Technology Institute (KEITI) through Environmental Health Action Program - Korea Ministry of Environment (MOE) [2018001360001]
  4. NIH/NHLBI [U01 HL137880, U24 HL141762]
  5. AstraZeneca/MedImmune
  6. Bellerophon Therapeutics
  7. Forest Research Institute, Inc.
  8. Grifols Therapeutics, Inc.
  9. Ikaria, Inc.
  10. Novartis Pharmaceuticals Corporation
  11. Nycomed GmbH
  12. Regeneron Pharmaceuticals, Inc.
  13. Sanofi
  14. Sunovion
  15. Takeda Pharmaceutical Company
  16. Theravance Biopharma
  17. Mylan

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This study utilized a deep learning network combined with factor analysis to analyze lung tissue patterns in COPD patients, discovering new latent factors that can predict pulmonary function. The findings suggest that factor-based surrogate markers may aid in discerning different disease severity stages among COPD patients.
Chronic obstructive pulmonary disease (COPD) is a heterogeneous disease and the traditional variables extracted from computed tomography (CT) images may not be sufficient to describe all the topological features of lung tissues in COPD patients. We employed an unsupervised three-dimensional (3D) convolutional autoencoder (CAE)-feature constructor (FC) deep learning network to learn from CT data and derive tissue pattern-clusters jointly. We then applied exploratory factor analysis (EFA) to discover the unobserved latent traits (factors) among pattern-clusters. CT images at total lung capacity (TLC) and residual volume (RV) of 541 former smokers and 59 healthy non-smokers from the cohort of the SubPopulations and Intermediate Outcome Measures in the COPD Study (SPIROMICS) were analyzed. TLC and RV images were registered to calculate the Jacobian (determinant) values for all the voxels in TLC images. 3D Regions of interest (ROIs) with two data channels of CT intensity and Jacobian value were randomly extracted from training images and were fed to the 3D CAE-FC model. 80 pattern-clusters and 7 factors were identified. Factor scores computed for individual subjects were able to predict spirometry-measured pulmonary functions. Two factors which correlated with various emphysema subtypes, parametric response mapping (PRM) metrics, airway variants, and airway tree to lung volume ratio were discriminants of patients across all severity stages. Our findings suggest the potential of developing factor-based surrogate markers for new COPD phenotypes.

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