Evidence map›Paper›PMID 24393332›Full record

ArticleBMC medical imaging2014

Automated measurement of heterogeneity in CT images of healthy and diseased rat lungs using variogram analysis of an octree decomposition.

Richard E Jacob, James P Carson

Abstract read
In one paragraph

Article in BMC medical imaging, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. The textures of sarcoidosis: quantifying lung disease through variograms.medRxiv : the preprint server for health sciences · 2024
    Article
  3. Article
  4. Article
  5. Magnetic resonance imaging provides sensitive in vivo assessment of experimental ventilator-induced lung injury.American journal of physiology. Lung cellular and molecular physiology · 2016
    Article
  6. Article
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Richard E JacobBiological Sciences Division, Pacific Northwest National Laboratory, 902 Battelle Blvd,, Richland, WA 99352, USA. richard.jacob@pnnl.gov.
James P Carson

Funding

3D IMAGING &COMPUTER MODEL OF THE RESPIRATORY TRACTR01HL073598 · NHLBI · BATTELLE PACIFIC NORTHWEST LABORATORIES · PI CORLEY, RICHARD A · 2004 to 2014
$17.6M
NHLBI NIH HHS R01HL073598
6 · The paper itself

Abstract

backgroundAssessing heterogeneity in lung images can be an important diagnosis tool. We present a novel and objective method for assessing lung damage in a rat model of emphysema. We combined a three-dimensional (3D) computer graphics method-octree decomposition-with a geostatistics-based approach for assessing spatial relationships-the variogram-to evaluate disease in 3D computed tomography (CT) image volumes.

methodsMale, Sprague-Dawley rats were dosed intratracheally with saline (control), or with elastase dissolved in saline to either the whole lung (for mild, global disease) or a single lobe (for severe, local disease). Gated 3D micro-CT images were acquired on the lungs of all rats at end expiration. Images were masked, and octree decomposition was performed on the images to reduce the lungs to homogeneous blocks of 2 × 2 × 2, 4 × 4 × 4, and 8 × 8 × 8 voxels. To focus on lung parenchyma, small blocks were ignored because they primarily defined boundaries and vascular features, and the spatial variance between all pairs of the 8 × 8 × 8 blocks was calculated as the square of the difference of signal intensity. Variograms-graphs of distance vs. variance-were constructed, and results of a least-squares-fit were compared. The robustness of the approach was tested on images prepared with various filtering protocols. Statistical assessment of the similarity of the three control rats was made with a Kruskal-Wallis rank sum test. A Mann-Whitney-Wilcoxon rank sum test was used to measure statistical distinction between individuals. For comparison with the variogram results, the coefficient of variation and the emphysema index were also calculated for all rats.

resultsVariogram analysis showed that the control rats were statistically indistinct (p = 0.12), but there were significant differences between control, mild global disease, and severe local disease groups (p < 0.0001). A heterogeneity index was calculated to describe the difference of an individual variogram from the control average. This metric also showed clear separation between dose groups. The coefficient of variation and the emphysema index, on the other hand, did not separate groups.

conclusionThese results suggest the octree decomposition and variogram analysis approach may be a rapid, non-subjective, and sensitive imaging-based biomarker for characterizing lung disease.

Indexed as

AnimalsDisease Models, AnimalEmphysemaImaging, Three-DimensionalLungMaleRadiographic Image Interpretation, Computer-AssistedRatsRats, Sprague-DawleySensitivity and SpecificityTomography, X-Ray Computed

Identifiers

PMID24393332
PMCPMC3922839

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.