4.5 Article

Cerebral blood volume mapping using Fourier-transform-based velocity-selective saturation pulse trains

Journal

MAGNETIC RESONANCE IN MEDICINE
Volume 81, Issue 6, Pages 3544-3554

Publisher

WILEY
DOI: 10.1002/mrm.27668

Keywords

arterial spin labeling; cerebral blood volume; eddy current; Fourier-transform-based velocity-selective saturation; velocity-selective pulse train

Funding

  1. NIH [R01 HL138182, K25 HL121192, R01 HL135500]
  2. Scholar Award of American Society of Hematology [P41 EB015909]
  3. National Research Foundation of Korea [2018R1D1A1B07045267]
  4. National Research Foundation of Korea [2018R1D1A1B07045267] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Purpose: Velocity-selective saturation (VSS) pulse trains provide a viable alternative to the spatially selective methods for measuring cerebral blood volume (CBV) by reducing the sensitivity to arterial transit time. This study is to compare the Fourier-transformbased velocity-selective saturation (FT-VSS) pulse trains with the conventional flow-dephasing VSS techniques for CBV quantification. Methods: The proposed FT-VSS label and control modules were compared with VSS pulse trains utilizing double refocused hyperbolic tangent (DRHT) and 8-segment B1-insensitive rotation (BIR-8). This was done using both numerical simulations and phantom studies to evaluate their sensitivities to gradient imperfections such as eddy currents. DRHT, BIR-8, and FT-VSS prepared CBV mapping was further compared for velocity-encoding gradients along 3 orthogonal directions in healthy subjects at 3T. Results: The phantom studies exhibited more consistent immunity to gradient imperfections for the utilized FT-VSS pulse trains. Compared to DRHT and BIR-8, FT-VSS delivered more robust CBV results across the 3 VS encoding directions with significantly reduced artifacts along the superior-inferior direction and improved temporal signal-to-noise ratio (SNR) values. Average CBV values obtained from FT-VSS based sequences were 5.3 mL/100 g for gray matter and 2.3 mL/100 g for white matter, comparable to literature expectations. Conclusion: Absolute CBV quantification utilizing advanced FT-VSS pulse trains had several advantages over the existing approaches using flow-dephasing VSS modules. A greater immunity to gradient imperfections and the concurrent tissue background suppression of FT-VSS pulse trains enabled more robust CBV measurements and higher SNR than the conventional VSS pulse trains.

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