Modeling Dynamic Contrast-Enhanced MRI Data with a Constrained Local AIF.

Purpose: This study aims to develop a constrained local arterial input function (cL-AIF) to improve quantitative analysis of dynamic contrast-enhanced (DCE)-magnetic resonance imaging (MRI) data by accounting for the contrast-agent bolus amplitude error in the voxel-specific AIF.Procedures: Bayesian...

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Publicado en:Molecular Imaging & Biology Vol. 20; no. 1; pp. 150 - 160
Autores principales: Duan, Chong, Kallehauge, Jesper F., Pérez-Torres, Carlos J., Bretthorst, G. Larry, Beeman, Scott C., Tanderup, Kari, Ackerman, Joseph J. H., Garbow, Joel R.
Formato: equations & formulas research tables/charts Journal Article
Publicado: Springer Nature Feb2018
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Feb2018
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      pub: Springer Nature
      place: New York, New York
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        10.1007/s11307-017-1090-x
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        atl: Modeling Dynamic Contrast-Enhanced MRI Data with a Constrained Local AIF.
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        au:
          Duan, Chong
          Kallehauge, Jesper F.
          Pérez-Torres, Carlos J.
          Bretthorst, G. Larry
          Beeman, Scott C.
          Tanderup, Kari
          Ackerman, Joseph J. H.
          Garbow, Joel R.
        affil: Department of Chemistry, Washington University, Saint Louis, MO, USA
      sug:
        subj:
          Magnetic Resonance Imaging
          Algorithms
          Contrast Media
          Models, Biological
          Kinetics
          Computer Simulation
          Time Factors
          Uncertainty
          Funding Source
      ab: Purpose: This study aims to develop a constrained local arterial input function (cL-AIF) to improve quantitative analysis of dynamic contrast-enhanced (DCE)-magnetic resonance imaging (MRI) data by accounting for the contrast-agent bolus amplitude error in the voxel-specific AIF.Procedures: Bayesian probability theory-based parameter estimation and model selection were used to compare tracer kinetic modeling employing either the measured remote-AIF (R-AIF, i.e., the traditional approach) or an inferred cL-AIF against both in silico DCE-MRI data and clinical, cervical cancer DCE-MRI data.Results: When the data model included the cL-AIF, tracer kinetic parameters were correctly estimated from in silico data under contrast-to-noise conditions typical of clinical DCE-MRI experiments. Considering the clinical cervical cancer data, Bayesian model selection was performed for all tumor voxels of the 16 patients (35,602 voxels in total). Among those voxels, a tracer kinetic model that employed the voxel-specific cL-AIF was preferred (i.e., had a higher posterior probability) in 80 % of the voxels compared to the direct use of a single R-AIF. Maps of spatial variation in voxel-specific AIF bolus amplitude and arrival time for heterogeneous tissues, such as cervical cancer, are accessible with the cL-AIF approach.Conclusions: The cL-AIF method, which estimates unique local-AIF amplitude and arrival time for each voxel within the tissue of interest, provides better modeling of DCE-MRI data than the use of a single, measured R-AIF. The Bayesian-based data analysis described herein affords estimates of uncertainties for each model parameter, via posterior probability density functions, and voxel-wise comparison across methods/models, via model selection in data modeling.
      pubtype: Academic Journal
      doctype:
        equations & formulas
        research
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        Journal Article
      ougenre: Article
    language: English
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