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Optimization of adiabatic pulses for pulsed arterial spin labeling at 7 tesla: Comparison with pseudo‐continuous arterial spin labeling
Author(s) -
Wang Kai,
Shao Xingfeng,
Yan Lirong,
Ma Samantha J.,
Jin Jin,
Wang Danny J. J.
Publication year - 2021
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.28661
Subject(s) - specific absorption rate , amplitude , adiabatic process , imaging phantom , nuclear magnetic resonance , materials science , residual , arterial spin labeling , pulse sequence , offset (computer science) , perfusion , biomedical engineering , physics , optics , mathematics , algorithm , medicine , computer science , telecommunications , antenna (radio) , cardiology , thermodynamics , programming language
Purpose To optimize and evaluate adiabatic pulses for pulsed arterial spin labeling at ultrahigh field 7 tesla. Methods Four common adiabatic inversion pulses, including hyperbolic secant, wideband uniform rate smooth truncation, frequency offset corrected inversion, and time‐resampled frequency offset corrected inversion pulses, were optimized based on a custom‐defined loss function that included labeling efficiency and inversion band uniformity. The optimized pulses were implemented in flow‐sensitive alternating inversion recovery sequences and tested on phantom and 11 healthy volunteers with 2 constraints: 1) specific absorption rate normalized; and 2) equal peak RF amplitude, respectively. A pseudo‐continuous arterial spin labeling sequence was implemented for comparison. Quantitative metrics such as perfusion and relative labeling efficiency versus residual tissue signal were calculated. Results Among the 4 pulses, the wideband uniform rate smooth truncation pulse yielded the lowest loss in simulation and achieved a good balance between labeling efficiency and residual tissue signal from both phantom and in vivo experiments. Wideband uniform rate smooth truncation–pulsed arterial spin labeling showed significantly higher relative labeling efficiency compared to the other sequences ( P < .01), whereas the perfusion signal was increased by 40% when the highest B 1 + amplitude was used. The 4 pulsed arterial spin labeling sequences yielded comparable perfusion signals compared to pseudo‐continuous arterial spin labeling but with less than half the specific absorption rate. Conclusion Optimized wideband uniform rate smooth truncation pulse with the highest B 1 + amplitude allowed was recommended for 7 tesla pulsed arterial spin labeling.