• DocumentCode
    1171332
  • Title

    Distributed versus compartment models for PET receptor studies

  • Author

    Muzic, Raymond F., Jr. ; Saidel, Gerald M.

  • Author_Institution
    Dept. of Nucl. Medicine, Case Western Reserve Univ., Cleveland, OH, USA
  • Volume
    22
  • Issue
    1
  • fYear
    2003
  • Firstpage
    11
  • Lastpage
    21
  • Abstract
    Although distributed models are generally accepted as being more realistic than compartment models, use of simpler compartment models is pervasive in nuclear medicine applications, particularly in positron emission tomography (PET). Here, we report on comparisons made between distributed and compartment model outputs to address the question of whether differences between them are sufficient to justify distributed models for analysis of PET receptor experiments. For both two- and three-injection experiments, "data" sets were obtained by simulation using a distributed model and a wide range of parameter values. Optimal fits of the compartment model output to these "data" were achieved with three strategies in which values of different groups of parameter were estimated. Compartment model outputs yielded good fits to all the distributed model outputs and the values of the corresponding parameters were in close agreement. Given the temporal resolution typically available with PET, the use of a distributed model has no advantage over a compartment model for PET receptor quantification.
  • Keywords
    blood flow measurement; physiological models; positron emission tomography; PET receptor quantification; compartment models; data sets; distributed models; nuclear medicine; optimal fits; parameter values; positron emission tomography; temporal resolution; three-injection experiments; two-injection experiments; Biomedical engineering; Blood; Context modeling; Data mining; Heart; Lungs; Nuclear medicine; Parameter estimation; Positron emission tomography; Spatial resolution; Computer Simulation; Heart; Humans; Ligands; Metabolic Clearance Rate; Models, Biological; Models, Cardiovascular; Models, Chemical; Myocardium; Radiopharmaceuticals; Receptors, Cell Surface; Reproducibility of Results; Sensitivity and Specificity; Tomography, Emission-Computed;
  • fLanguage
    English
  • Journal_Title
    Medical Imaging, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    0278-0062
  • Type

    jour

  • DOI
    10.1109/TMI.2002.806576
  • Filename
    1191356