TY - JOUR
T1 - Ensuring both velocity and spatial responses robust to B0/B1+ field inhomogeneities for velocity-selective arterial spin labeling through dynamic phase-cycling
AU - Liu, Dapeng
AU - Li, Wenbo
AU - Xu, Feng
AU - Zhu, Dan
AU - Shin, Taehoon
AU - Qin, Qin
N1 - Publisher Copyright:
© 2020 International Society for Magnetic Resonance in Medicine
PY - 2021/5
Y1 - 2021/5
N2 - Purpose: To evaluate both velocity and spatial responses of velocity-selective arterial spin labeling (VS-ASL), using velocity-insensitive and velocity-compensated waveforms for control modules, as well as a novel dynamic phase-cycling approach, at different B0/ (Formula presented.) field inhomogeneities. Methods: In the presence of imperfect refocusing, the mechanism of phase-cycling the refocusing pulses through four dynamics was first theoretically analyzed with the conventional velocity-selective saturation (VSS) pulse train. Numerical simulations were then deployed to compare the performance of the Fourier-transform based velocity-selective inversion (FT-VSI) with these three different schemes in terms of both velocity and spatial responses under various B0/ (Formula presented.) conditions. Phantom and human brain scans were performed to evaluate the three methods at (Formula presented.) scales of 0.8, 1.0, and 1.2. Results: The simulations of FT-VSI showed that, under nonuniform B0/ (Formula presented.) conditions, the scheme with velocity-insensitive control was susceptible to DC bias of the static spins as systematic error, while the scheme with velocity-compensated control had deteriorated velocity-selective labeling profiles and, thus, reduced labeling efficiency. Through numerical simulation, phantom scans, and brain perfusion measurements, the dynamic phase-cycling method demonstrated considerable improvements over these issues. Conclusion: The proposed dynamic phase-cycling approach was demonstrated for the velocity-selective label and control modules with both velocity and spatial responses robust to a wide range of B0 and (Formula presented.) field inhomogeneities.
AB - Purpose: To evaluate both velocity and spatial responses of velocity-selective arterial spin labeling (VS-ASL), using velocity-insensitive and velocity-compensated waveforms for control modules, as well as a novel dynamic phase-cycling approach, at different B0/ (Formula presented.) field inhomogeneities. Methods: In the presence of imperfect refocusing, the mechanism of phase-cycling the refocusing pulses through four dynamics was first theoretically analyzed with the conventional velocity-selective saturation (VSS) pulse train. Numerical simulations were then deployed to compare the performance of the Fourier-transform based velocity-selective inversion (FT-VSI) with these three different schemes in terms of both velocity and spatial responses under various B0/ (Formula presented.) conditions. Phantom and human brain scans were performed to evaluate the three methods at (Formula presented.) scales of 0.8, 1.0, and 1.2. Results: The simulations of FT-VSI showed that, under nonuniform B0/ (Formula presented.) conditions, the scheme with velocity-insensitive control was susceptible to DC bias of the static spins as systematic error, while the scheme with velocity-compensated control had deteriorated velocity-selective labeling profiles and, thus, reduced labeling efficiency. Through numerical simulation, phantom scans, and brain perfusion measurements, the dynamic phase-cycling method demonstrated considerable improvements over these issues. Conclusion: The proposed dynamic phase-cycling approach was demonstrated for the velocity-selective label and control modules with both velocity and spatial responses robust to a wide range of B0 and (Formula presented.) field inhomogeneities.
KW - B field inhomogeneity
KW - B1+ field inhomogeneity
KW - arterial spin labeling
KW - cerebral blood flow
KW - velocity-selective inversion
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U2 - 10.1002/mrm.28622
DO - 10.1002/mrm.28622
M3 - Article
C2 - 33349968
AN - SCOPUS:85097287011
SN - 0740-3194
VL - 85
SP - 2723
EP - 2734
JO - Magnetic resonance in medicine
JF - Magnetic resonance in medicine
IS - 5
ER -