UCT Medical Imaging Research Unit, Division of Biomedical Engineering, Department of Human Biology, University of Cape Town, Cape Town, South Africa.
Athinoula A. Martinos Center for Biomedical Imaging/MGH, Charlestown, Massachusetts.
Magn Reson Med. 2019 Apr;81(4):2600-2613. doi: 10.1002/mrm.27597. Epub 2018 Dec 2.
CEST MRI allows for indirect detection of molecules with exchangeable protons, measured as a reduction in water signal because of continuous transfer of saturated protons. CEST requires saturation pulses on the order of a second, as well as repeated acquisitions at different offset frequencies. The resulting extended scan time makes CEST susceptible to subject motion, which introduces field inhomogeneity, shifting offset frequencies and causing distortions in CEST spectra that resemble true CEST effects. This is a particular problem for molecules that resonate close to water, such as hydroxyl group in glycogen. To address this, a technique for real-time measurement and correction of motion and field inhomogeneity is proposed.
A CEST sequence was modified to include double volumetric navigators (DvNavs) for real-time simultaneous motion and shim correction. Phantom tests were conducted to investigate the effects of motion and shim changes on CEST quantification and to validate the accuracy of DvNav motion and shim estimates. To evaluate DvNav shim and motion correction in vivo, acquisitions including 5 experimental conditions were performed in the calf muscle of 2 volunteers.
Phantom data show that DvNav-CEST accurately estimates frequency and linear gradient changes because of motion and corrects resulting image distortions. In addition, DvNav-CEST improves CEST quantification in vivo in the presence of motion.
The proposed technique allows for real-time simultaneous motion and shim correction with no additional scanning time, enabling accurate CEST quantification even in the presence of motion and field inhomogeneity.
化学交换饱和转移(CEST)MRI 允许间接检测可交换质子的分子,其表现为由于饱和质子的连续转移导致水信号减少。CEST 需要持续时间约为 1 秒的饱和脉冲,以及在不同偏移频率下重复采集。由此产生的扩展扫描时间使 CEST 容易受到受试者运动的影响,这会引入磁场不均匀性,改变偏移频率,并导致 CEST 谱的扭曲,这些扭曲类似于真正的 CEST 效应。对于与水共振的分子,如糖原中的羟基基团,这是一个特别的问题。为了解决这个问题,提出了一种用于实时测量和校正运动和磁场不均匀性的技术。
修改了 CEST 序列,包括双容积导航仪(DvNavs),用于实时同时进行运动和匀场校正。进行了幻影测试,以研究运动和匀场变化对 CEST 定量的影响,并验证 DvNav 运动和匀场估计的准确性。为了在体内评估 DvNav 匀场和运动校正,在 2 名志愿者的小腿肌肉中进行了包含 5 种实验条件的采集。
幻影数据表明,DvNav-CEST 可以准确估计由于运动引起的频率和线性梯度变化,并校正由此产生的图像扭曲。此外,DvNav-CEST 可以在存在运动的情况下改善体内 CEST 定量。
所提出的技术允许实时同时进行运动和匀场校正,而不会增加额外的扫描时间,即使在存在运动和磁场不均匀性的情况下,也能实现准确的 CEST 定量。