Dan Zhu1,2, Dapeng Liu2,3, Wenbo Li2,3, Michael Schär2, and Qin Qin2,3
1Department of Biomedical Engineering, Johns Hopkins University School of Medicine, Baltimore, MD, United States, 2Russell H. Morgan Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD, United States, 3. F.M. Kirby Research Center for Functional Brain Imaging, Johns Hopkins University School of Medicine, Baltimore, MD, United States
Synopsis
Renal perfusion
has clinical significance in diagnosis of renal diseases. Velocity-selective arterial
spin labeling (VSASL) has minimal sensitivity to arterial transit time delay and velocity-selective
inversion (VSI) labeling could improve SNR of perfusion signal. Here renal VSASL images were acquired using different
post-labeling delay time and under different B1 shimming conditions. The
feasibility of VSI based ASL for renal perfusion mapping at 3T under free
breathing is demonstrated on healthy volunteers.
Introduction
Perfusion quantification is important
for accessing renal tissue function of both chronic kidney disease and acute
kidney injuries, as well as characterizing renal cell carcinoma1,2. Arterial
spin labeling (ASL) does not require injecting contrast agents and is ideally
suited for kidney perfusion measurement especially for patients with renal
insufficiency3. ASL methods based on spatially selective labeling,
such as FAIR and PCASL, have been demonstrated mostly at 1.5T4-9 with
fewer on 3T10-12. Spatially selective ASL
is known to be sensitive to extended
arterial transit time, especially for patients with renal artery stenosis.
Velocity-selective (VS) ASL has minimal time-delay
sensitivity13 and was recently shown feasible for renal ASL at 1.5T14. Compared
to conventional flow-dephasing based VS saturation (VSS) pulse train, Fourier-transform
(FT) based VS inversion (VSI) pulse train was demonstrated with higher SNR for brain perfusion
measurement at 3T15. Both spatially selective
and velocity-selective ASL methods are susceptible to the stronger B0 and B1
field inhomogeneities in the abdomen at 3T. In this work we aim to evaluate the
feasibility of VSI prepared ASL on renal perfusion mapping at 3T.Methods
The diagram for the VSI prepared renal ASL
sequence is shown in Fig.1a. A pre-saturation pulse was applied with 2000ms
delay allowing arterial inflow. The VSI pulse train was composed of nine 20° excitation
pulses, interleaved with 16 phase-cycled composite refocusing pulses with bipolar
or unipolar velocity-encoding gradients for velocity-sensitive label and velocity-compensated control modules respectively (Fig.1b). The pulse was 64ms long and the cutoff velocity
(Vc) was 2cm/s.
The ideal velocity-selective profile of this VSI pulse train is shown in Fig.1c. During Post labeling delay (PLD), three
non-selective adiabatic inversion pulses were applied for background
suppression (BGS). At the end of the PLD, a 20ms T2 preparation VSS module was
applied before fat suppression and acquisition to dephase blood spins flowing
above 3cm/s. The velocity-encoding gradients of both the VSI and VSS pulses were
applied along the left-right direction of bilateral kidney arteries. This also
avoided mistakenly labeling the foot-head motion of renal tissue during
respiration.
A Bloch equation simulation was conducted to assess
the sensitivity of label efficiency to B0 and B1 inhomogeneities. The B1 range was
60% to 120% with B0 off-resonance set to either 0Hz or -50Hz.
Experiments
were conducted among seven
healthy volunteers (24-59 yo, 4 females) at a 3T Philips Ingenia scanner with a
32-channel chest array. PLD of 0.6s, 0.9s, and 1.2s were compared with the
timing of BGS pulses listed in Fig.1d. We also compared the performance of fixed and vendor-provided adaptive RF
shimming (dual-transmit) with local power setting. A 2D coronal slice was
acquired with single-shot GRASE during free breathing: FOV=200(FH)$$$\times$$$400(LR)mm2,
Resolution=2$$$\times$$$2mm2, slice thickness=8mm, TSE factor=6, EPI factor=15,
SENSE=2, TE=17ms, TR=3045/3345/3645ms for each PLD, 16 dynamics of control-label
pairs. M0 maps were acquired with the same acquisition except TR=5000ms. Cortex
images were acquired using inversion recovery with TI=1300ms. B0 maps were obtained by a standard gradient echo sequences with two echo times. Auto B0 shim was used in all scans. Dream
technique16 was used to obtain B1+ maps with
STEAM flip angle = 60° and imaging flip angle =20°.
Image alignment
was implemented on Advanced Normalization Toolkit libraries (ANTs)17, with non-rigid registration after an affine
registration. Control and label series were registered to an individual control
image and then averaged to obtain the reference for M0 registration. Renal
perfusion weighted signal (PWS) were analyzed as (control-lable)/M0. Temporal SNR (tSNR) of the labeling/control
difference images were calculated as the ratio of the mean to standard
deviation values.RESULTS AND DISCUSSION
Fig.2 shows the simulated Mz-velocity responses over different B0 and B1 conditions. When B1+ scales is more than 20% lower from the correct setting, the
velocity-selective profiles of the velocity-compensated control pulse train
increasingly deteriorate for the spins flowing above the cutoff velocity.
Even though the label module preserves the velocity-selective profiles under
these poor B0/B1conditions, the subtracted signal suffers very low labeling
efficiency.
PWS and
tSNR images of a subject with different PLDs at two B1 shimming conditions are displayed
in Fig.3. Results with PLD=0.9s using adaptive shim of all seven subjects were arrayed in Fig.4, together
with B0 and B1 maps, M0 and cortex images, as well as averaged control and label images
normalized by M0. Good quality
of renal perfusion weighted images were seen in first six cases, all with distinct
cortex-medulla contrast similar to the cortex images. The last case yielded low
perfusion signal in the right kidney, most likely affected by the poor B1
inhomogeneity as reflected in the corresponding B1 map.
The
averaged PWS and tSNR within cortex region of interest for the six successful
cases with different PLD and B1 shim conditions are compared in Fig.5. Results indicated
better performance with Adaptive B1 Shim than fixed shim on both PWS and tSNR. PLD=0.9s
also derived slightly higher perfusion signal and tSNR than 0.6s and 1.2s
delays.CONCLUSION
The
feasibility of VSI based ASL for renal perfusion mapping at 3T under free
breathing is demonstrated on healthy volunteers. Better B1 shimming will be
explored in future work to improve the robustness of the method.Acknowledgements
No acknowledgement found.References
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