In this work, a modified pseudo-continuous ASL sequence is presented, which reduces the SAR deposition by ~50% and provides robust labeling efficiency in the presence of off-resonances between -300Hz and 300Hz. The sequence was successfully tested on two coils with different coverage of the neck region at two labeling positions. The method allows PCASL experiments at UHF without a pre-scan in significantly reduced scan time and, therefore, exploits the advantage of UHF for perfusion imaging.
Pseudo-continuous ASL (PCASL)(1) has many advantages at ultra-high field (UHF >3T)(2). Most prominent are the longer T1,blood, leading to slower decay of the label, and the intrinsically higher SNR. But the rapid application of thousands of RF pulses causes significant energy deposition (SAR) forcing the user to use longer TRs, which decreases the sensitivity per unit time. A second problem is the loss of labeling efficiency in the presence of B0 inhomogeneities, which can lead to a nonuniform labeling across the brain feeding arteries(3),(2).
In this work, modifications to the PCASL pulse train are presented, which reduce the SAR deposition and increase the robustness against off-resonances by means of shorter pulse spacing and variable rate RF pulses. This enables a prescan-free acquisition of background-suppressed whole brain PCASL at 7T within a TR of 8s.
PCASL labeling was simulated as described in (3) to find optimal pulse spacing and duration. The parameter set presented in the aforementioned publication (unbalanced PCASL at 3T, TPulse=500 µs, TSpacing=1200 µs, B1,avg=1.5 µT, gmax=3.5 mT/m, gaverage=0.5 mT/m) served as a starting point for further optimization. Since the off-resonance effects of PCASL are a direct result of the introduced gaps between RF pulses, the gaps were minimized. The pulse duration maximized to distribute the RF energy deposition over as much time as possible to reduce SAR. Along with hardware restrictions due to acoustic resonance frequencies of the gradient system, gradient limits and RF duty cycles, this leads to a pulse spacing of 600 µs and a pulse duration of 420 µs. To further reduce SAR, the VERSE scheme presented in (4) was applied to the Hann-shaped RF pulses and corresponding gradients, significantly reducing RF amplitude while timing is maintained. The initial PCASL sequence (PCASL3T) and the optimized one (PCASL7T) are shown in Fig. 1.
This PCASL scheme was implemented on a Siemens Magnetom 7T (Siemens Healthineers, Erlangen) equipped with an additional parallel transmit (pTX) system (8-channel, version 2.3). A centric-reordered gradient echo 3D-EPI readout was used, which helps to minimize SAR due to its small excitation flip angles. For background suppression a WET(5) pre-saturation with 4 pulses and two GOIA-WURST-16-4(6) pulses (6.7 ms duration, 16.8 kHz bandwidth, 14 µT B1,max) for inversion were used.
Two subjects (2 female, 34 +/- 6 years) were scanned at 7T. The imaging protocol included a flip angle map (3D-DREAM)(7), a B0 shimming sequence, an anatomical MPRAGE scan (1mm3) and a PCASL scan (Resolution=2.5x2.5x2.5 mm3, TE=6.8 ms, TR=8 s, GRAPPAPE1=2x, Partial-fourier-factorPE1=6/8, repetitions=22, acquisition time=02m:56s, labeling duration=1.5s, PLD=1.5s). Reference voltages were derived from the flip angle map and the PCASL pulse voltage was then increased by 25% to mitigate low transmission efficiency in the neck region. The first subject was scanned in single channel transmit mode at labeling position (a) as shown in Fig. 3. The second subject was scanned with the 8-channel pTX system in so called protected mode (conservative RF power limits given by global worst-case estimates). Here, labeling position (b) as in Fig. 3 was possible, since the flip angle map indicated a more efficient transmission in the lower regions for the pTX coil (32RX/8TX Nova Medical) compared to the single channel transmit coil (32RX/1TX Nova Medical).
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