EBioMedicine (Oct 2015)

Grating-based X-ray Dark-field Computed Tomography of Living Mice

  • A. Velroyen,
  • A. Yaroshenko,
  • D. Hahn,
  • A. Fehringer,
  • A. Tapfer,
  • M. Müller,
  • P.B. Noël,
  • B. Pauwels,
  • A. Sasov,
  • A.Ö. Yildirim,
  • O. Eickelberg,
  • K. Hellbach,
  • S.D. Auweter,
  • F.G. Meinel,
  • M.F. Reiser,
  • M. Bech,
  • F. Pfeiffer

DOI
https://doi.org/10.1016/j.ebiom.2015.08.014
Journal volume & issue
Vol. 2, no. 10
pp. 1500 – 1506

Abstract

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Changes in x-ray attenuating tissue caused by lung disorders like emphysema or fibrosis are subtle and thus only resolved by high-resolution computed tomography (CT). The structural reorganization, however, is of strong influence for lung function. Dark-field CT (DFCT), based on small-angle scattering of x-rays, reveals such structural changes even at resolutions coarser than the pulmonary network and thus provides access to their anatomical distribution. In this proof-of-concept study we present x-ray in vivo DFCTs of lungs of a healthy, an emphysematous and a fibrotic mouse. The tomographies show excellent depiction of the distribution of structural – and thus indirectly functional – changes in lung parenchyma, on single-modality slices in dark field as well as on multimodal fusion images. Therefore, we anticipate numerous applications of DFCT in diagnostic lung imaging. We introduce a scatter-based Hounsfield Unit (sHU) scale to facilitate comparability of scans. In this newly defined sHU scale, the pathophysiological changes by emphysema and fibrosis cause a shift towards lower numbers, compared to healthy lung tissue.

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