MRI-derived arterial input functions for PET kinetic modelling in rats

被引:3
|
作者
Evans, Eleanor [1 ]
Sawiak, Stephen J. [1 ,2 ]
Carpenter, T. Adrian [1 ]
机构
[1] Univ Cambridge, Addenbrookes Hosp, Wolfson Brain Imaging Ctr, Cambridge CB2 2QQ, England
[2] Univ Cambridge, Behav & Clin Neurosci Inst, Cambridge, England
来源
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT | 2013年 / 702卷
基金
英国医学研究理事会;
关键词
PET/MR; MRI; PET; Arterial input function; Rats; Contrast agent; TIME;
D O I
10.1016/j.nima.2012.08.081
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
Simultaneous PET-MR acquisition provides the high temporal and spatial resolution of MRI with the specificity of PET. In PET, accurate modelling of physiological function in vivo requires the time-activity curve of tracer in blood plasma, known as the arterial input function (ALF). As the gold standard method of blood sampling is inherently prohibitive in the small animal case, here we discuss how we prepare to rapidly sample MRI signals from gadolinium-doped tracer to obtain the tracer input functions from a simultaneous PET-MR measurement. Delta R2* measurements taken from EPI images were used to obtain first pass bolus AIFs in the rat brain from DSC-MRI datasets of 5 rats. AlFs obtained using our automatic algorithm were found to be consistent between animals and compared well with manual methods without need for a priori voxel selection. A variable flip angle FLASH sequence used for T1 mapping was successfully tested in a phantom study, providing accurate measurements of Gd concentration. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:126 / 128
页数:3
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