David A. Hormuth, II

Research Scientist | Biomedical Engineering + Imaging Science > > Computational Oncology

The effects of intravoxel contrast agent diffusion on the analysis of DCE‐MRI data in realistic tissue domains


Journal article


Ryan T Woodall, Stephanie L. Barnes, D. Hormuth, A. Sorace, C. Quarles, T. Yankeelov
Magnetic Resonance in Medicine, 2018

Semantic Scholar DOI PubMed
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APA   Click to copy
Woodall, R. T., Barnes, S. L., Hormuth, D., Sorace, A., Quarles, C., & Yankeelov, T. (2018). The effects of intravoxel contrast agent diffusion on the analysis of DCE‐MRI data in realistic tissue domains. Magnetic Resonance in Medicine.


Chicago/Turabian   Click to copy
Woodall, Ryan T, Stephanie L. Barnes, D. Hormuth, A. Sorace, C. Quarles, and T. Yankeelov. “The Effects of Intravoxel Contrast Agent Diffusion on the Analysis of DCE‐MRI Data in Realistic Tissue Domains.” Magnetic Resonance in Medicine (2018).


MLA   Click to copy
Woodall, Ryan T., et al. “The Effects of Intravoxel Contrast Agent Diffusion on the Analysis of DCE‐MRI Data in Realistic Tissue Domains.” Magnetic Resonance in Medicine, 2018.


BibTeX   Click to copy

@article{ryan2018a,
  title = {The effects of intravoxel contrast agent diffusion on the analysis of DCE‐MRI data in realistic tissue domains},
  year = {2018},
  journal = {Magnetic Resonance in Medicine},
  author = {Woodall, Ryan T and Barnes, Stephanie L. and Hormuth, D. and Sorace, A. and Quarles, C. and Yankeelov, T.}
}

Abstract

Quantitative evaluation of dynamic contrast enhanced MRI (DCE‐MRI) allows for estimating perfusion, vessel permeability, and tissue volume fractions by fitting signal intensity curves to pharmacokinetic models. These compart mental models assume rapid equilibration of contrast agent within each voxel. However, there is increasing evidence that this assumption is violated for small molecular weight gadolinium chelates. To evaluate the error introduced by this invalid assumption, we simulated DCE‐MRI experiments with volume fractions computed from entire histological tumor cross‐sections obtained from murine studies.


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