Simultaneous T1 and T2 mapping of hyperpolarized 13C compounds using the bSSFP sequence

被引:6
|
作者
Milshteyn, Eugene [1 ,3 ]
Reed, Galen D. [2 ]
Gordon, Jeremy W. [1 ]
von Morze, Cornelius [1 ,4 ]
Cao, Peng [1 ,5 ]
Tang, Shuyu [1 ]
Leynes, Andrew P. [1 ]
Larson, Peder E. Z. [1 ]
Vigneron, Daniel B. [1 ]
机构
[1] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, 1700 Fourth St,Byers Hall Suite 102, San Francisco, CA 94158 USA
[2] GE Healthcare, Dallas, TX USA
[3] Massachusetts Gen Hosp, Dept Radiol, Athinoula A Martins Ctr Biomed Imaging, Charlestown, MA USA
[4] Washington Univ, Dept Radiol, St Louis, MO USA
[5] HKU, Dept Diagnost Radiol, Hong Kong, Peoples R China
关键词
C-13; Hyperpolarized; T-1; T-2; Mapping; SSFP; MAGNETIC-RESONANCE; IN-VIVO; RELAXATION-TIMES; UREA; CANCER; PYRUVATE; MRI; TRANSLATION; METABOLISM; MODEL;
D O I
10.1016/j.jmr.2020.106691
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As in conventional H-1 MRI, T-1 and T-2 relaxation times of hyperpolarized (HP) C-13 nuclei can provide important biomedical information. Two new approaches were developed for simultaneous T-1 and T-2 mapping of HP C-13 probes based on balanced steady state free precession (bSSFP) acquisitions: a method based on sequential T-1 and T-2 mapping modules, and a model-based joint T-1/T-2 approach analogous to MR fingerprinting. These new methods were tested in simulations, HP C-13 phantoms, and in vivo in normal Sprague-Dawley rats. Non-localized T-1 values, low flip angle EPI T-1 maps, bSSFP T-2 maps, and Bloch-Siegert B-1 maps were also acquired for comparison. T-1 and T-2 maps acquired using both approaches were in good agreement with both literature values and data from comparative acquisitions. Multiple HP C-13 compounds were successfully mapped, with their relaxation time parameters measured within heart, liver, kidneys, and vasculature in one acquisition for the first time. (C) 2020 Elsevier Inc. All rights reserved.
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页数:9
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