4.5 Article

Ensuring both velocity and spatial responses robust to B-0/B-1(+) field inhomogeneities for velocity-selective arterial spin labeling through dynamic phase-cycling

Journal

MAGNETIC RESONANCE IN MEDICINE
Volume 85, Issue 5, Pages 2723-2734

Publisher

WILEY
DOI: 10.1002/mrm.28622

Keywords

B-1(+) field inhomogeneity; arterial spin labeling; B-0 field inhomogeneity; cerebral blood flow; velocity-selective inversion

Funding

  1. NIH [R01 HL138182, R01 HL144751, R01 HL135500, K25 HL145129]
  2. Scholar Award of American Society of Hematology
  3. NIH

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The study aimed to evaluate the velocity and spatial responses of velocity-selective arterial spin labeling under different field inhomogeneities. Numerical simulations and human scans showed that the dynamic phase-cycling approach significantly improved the labeling efficiency and control module performance under nonuniform field conditions.
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 B-0/B-1(+) 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 B-0/B(1)(+ )conditions. Phantom and human brain scans were performed to evaluate the three methods at B-1(+) scales of 0.8, 1.0, and 1.2. Results: The simulations of FT-VSI showed that, under nonuniform B-0/B-1(+) 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 B-0 and B-1(+) field inhomogeneities.

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