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.
引用
收藏
页数:9
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