Classic models for dynamic contrast-enhanced MRI

被引:330
|
作者
Sourbron, Steven P. [1 ]
Buckley, David L. [1 ]
机构
[1] Univ Leeds, Div Med Phys, Leeds LS2 9JT, W Yorkshire, England
关键词
perfusion; permeability; tracer-kinetic models; deconvolution; DCE-MRI; DSC-MRI; CEREBRAL-BLOOD-FLOW; SINGULAR-VALUE DECOMPOSITION; BRAIN-BARRIER PERMEABILITY; GLOMERULAR-FILTRATION-RATE; TRACER-KINETIC-MODELS; BOLUS-TRACKING MRI; MAGNETIC-RESONANCE; GD-DTPA; SUSCEPTIBILITY-CONTRAST; GRADIENT-ECHO;
D O I
10.1002/nbm.2940
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Dynamic contrast-enhanced MRI (DCE-MRI) is a functional MRI method where T-1 -weighted MR images are acquired dynamically after bolus injection of a contrast agent. The data can be interpreted in terms of physiological tissue characteristics by applying the principles of tracer-kinetic modelling. In the brain, DCE-MRI enables measurement of cerebral blood flow (CBF), cerebral blood volume (CBV), blood-brain barrier (BBB) permeability-surface area product (PS) and the volume of the interstitium (v(e)). These parameters can be combined to form others such as the volume-transfer constant K-trans, the extraction fraction E and the contrast-agent mean transit times through the intra- and extravascular spaces. A first generation of tracer-kinetic models for DCE-MRI was developed in the early 1990s and has become a standard in many applications. Subsequent improvements in DCE-MRI data quality have driven the development of a second generation of more complex models. They are increasingly used, but it is not always clear how they relate to the models of the first generation or to the model-free deconvolution methods for tissues with intact BBB. This lack of understanding is leading to increasing confusion on when to use which model and how to interpret the parameters. The purpose of this review is to clarify the relation between models of the first and second generations and between model-based and model-free methods. All quantities are defined using a generic terminology to ensure the widest possible scope and to reveal the link between applications in the brain and in other organs. Copyright (C) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:1004 / 1027
页数:24
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