Comparison of dynamic contrast-enhanced MRI and quantitative SPECT in a rat glioma model

被引:11
|
作者
Skinner, Jack T. [1 ,2 ]
Yankeelov, Thomas E. [1 ,2 ,3 ,4 ,5 ]
Peterson, Todd E. [1 ,3 ,4 ]
Does, Mark D. [1 ,2 ,3 ]
机构
[1] Vanderbilt Univ, Inst Imaging Sci, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Biomed Engn, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Sch Med, Dept Radiol & Radiol Sci, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Dept Phys, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Dept Elect Engn, Dept Canc Biol, Nashville, TN 37232 USA
关键词
MRI; dynamic contrast; DCE; tumor; pharmacokinetic modeling; SPECT; radionuclide; diffusion; ARTERIAL INPUT FUNCTION; APPARENT DIFFUSION-COEFFICIENT; EXTRACELLULAR VOLUME FRACTION; DCE-MRI; TRACER KINETICS; BLOOD-VOLUME; WATER; TISSUE; PERMEABILITY; PARAMETERS;
D O I
10.1002/cmmi.1479
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Pharmacokinetic modeling of dynamic contrast-enhanced (DCE) MRI data provides measures of the extracellular-extravascular volume fraction (ve) and the volume transfer constant (Ktrans) in a given tissue. These parameter estimates may be biased, however, by confounding issues such as contrast agent and tissue water dynamics, or assumptions of vascularization and perfusion made by the commonly used model. In contrast to MRI, radiotracer imaging with SPECT is insensitive to water dynamics. A quantitative dual-isotope SPECT technique was developed to obtain an estimate of ve in a rat glioma model for comparison with the corresponding estimates obtained using DCE-MRI with a vascular input function and reference region model. Both DCE-MRI methods produced consistently larger estimates of ve in comparison to the SPECT estimates, and several experimental sources were postulated to contribute to these differences. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:494 / 500
页数:7
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