Niranjan Balu1, Zechen Zhou2, Thomas Hatsukami3, and Chun Yuan1
1Radiology, University of Washington, Seattle, WA, United States, 2Philips Healthcare, Briarcliff Manor, NY, United States, 3Surgery, University of Washington, Seattle, WA, United States
Synopsis
Vessel wall MRI requires good fat suppression to delineate
outer vessel boundaries. Large field-of-views required for turbo spin echo
femoral vessel wall MRI do not provide good fat suppression with spectral inversion
recovery. We developed a time-efficient two-point Dixon turbo spin echo method
using a SNR priority variable flip angle schedule and point spread correction
reconstruction to allow accelerated acquisition and demonstrate its advantages
compared to an existing gradient echo vessel wall MRI method.
Introduction
Large
coverage isotropic resolution vessel wall MRI (VWI) is challenging due to
competing requirements of scan time and signal-to-noise ratio (SNR). While
variable flip angle turbo spin echo MRI (VFA-TSE) sequences provide high SNR,
they do not provide effective or uniform fat suppression which is critical to
distinguish the outer boundary of the vessel wall. VFA-TSE fat suppression
tends to worsen further for large field-of-view (FOV) VWI such as femoral
artery VWI. While VFA-TSE has been demonstrated for VWI applications, their use
has been confined to either intracranial VWI [1] which does not require fat
suppression or smaller FOV VWI such as carotid VWI [2] or their combination [3,4].
Fat suppression for femoral VWI is particularly challenging since it requires a
large FOV starting from the groin to below the knees. Previous femoral VWI
methods have therefore used gradient echo-based sequences [5,6] which provide
sufficient (but non-uniform) fat suppression. While these gradient echo-based
methods are also time-efficient, they are highly susceptible to B0
inhomogeneity and do not provide uniform vessel signal over the large FOV.Aim
To develop a time efficient fat suppressed large FOV VFA-TSE
VWI sequence covering the femoral arteries from above the femoral bifurcation
to below the knees.Methods
A SNR priority variable flip angle schedule [7] was
optimized by Bloch-simulation (Simulation parameters: T1:844ms,T2:39ms,TSE:42,Startup
echoes:4,TR:1000ms) to determine the optimum VFA k-space filter
cutoff-frequency that provides higher signal than VFA-TSE with the sharpest
possible point-spread function (PSF). A k-space filter cutoff of 0.4 is optimal
by this criterion. Figure 1 shows the simulated VFA profiles and figure 2 shows
signal relative to a filter cutoff of 1.0 (highest possible PSF but lowest
signal). With cutoff held at 0.4, the effect of increasing TSE factor was
Bloch-simulated to determine the maximum possible acceleration possible using
large turbo factors (figure 3). SNR measurements were performed using a uniform
bottle phantom and separate noise scan (no RF pulse) to confirm simulation
predictions. All scans were conducted on a Philips Ingenia 3T CX whole body
scanner under IRB approved guidelines. Using optimized parameters from Bloch
simulation, VFA-TSE and 3D-MERGE [5] scans were then compared in vivo as
follows: VFA-TSE with two-point Dixon fat-suppression [8] and similar scan time
as 3D-MERGE was scanned in two stations (40cm S/I FOV each) with a 5cm overlap
between stations. In vivo imaging parameters were optimized on one volunteer
and are shown in table 1. Dixon VFA-TSE, 3D-MERGE and VFA-TSE with spectral
adiabatic inversion recovery fat suppression (SPAIR) were compared in a
volunteer. In vivo SNR priority VFA-TSE scans were PSF corrected using a PSF
correction neural network [7]. Fat suppression, outer wall visibility and SNR
were compared between VFA-TSE and 3D-MERGE. Muscle signal, fat signal in adjacent region
and lumen signal were measured in the thigh. Noise was measured as the standard
deviation of muscle signal to account for use of phased array coils. Muscle-fat
contrast-to-noise ratio (CNRmf) and muscle-lumen CNR (CNRml)
were also compared. Results
A k-space filter cutoff of 0.4 was predicted to provide 2.88x
times the signal relative to cutoff of 1.0 and was used as the optimum cutoff
for in vivo scans. SNR measurements on phantom confirmed simulation
predictions. Increasing TSE was predicted to reduce SNR but not impact PSF. SNR
measurement on a phantom using VFA-TSE and 3D-MERGE showed that TSE factors up
to 85 can be used without SNR penalty relative to 3D-MERGE. In vivo
optimization scans showed that four startup echoes provided sufficient blood
suppression. A TSE factor 75 provided similar scan time as 3D-MERGE. 2X SENSE
acceleration was additionally used for Dixon VFA-TSE only. Two-point Dixon
provided uniform fat suppression for accelerated VFA-TSE across the entire FOV
(figure 4) visually comparable to 3D-MERGE. Signal homogeneity was
substantially better on Dixon VFA-TSE compared to 3D-MERGE, which suffered from
flame artifacts and overall reduced SNR at the edges of the FOV.
Muscle SNR was substantially higher on Dixon VFA-TSE compared
to 3D-MERGE (33.6±5.4 vs 14.2±3.9, p<0.05). CNRmf was
similar on Dixon VFA-TSE and 3D-MERGE (0.5±0.1 vs 0.1±0.4, p=0.16) showing that fat
suppression was adequate on Dixon VFA-TSE for identifying vessel wall. However,
the much lower standard deviation of Dixon VFA-TSE compared to 3D-MERGE suggests
uniform fat suppression on Dixon VFA-TSE while 3D-MERGE fat suppression was
non-uniform. CNRmf was higher on Dixon VFA-TSE than 3D-MERGE
(0.7±0.0
vs 0.5±0.0, p<0.05) suggesting better blood suppression than
3D-MERGE. Compared to SPAIR VFA-TSE, Dixon VFA-TSE had substantially higher CNRmf
(0.7±0.0
vs 0.0±0.14, p<0.05) showing that fat suppression was
significantly improved with Dixon VFA-TSE.Conclusions
A novel acceleration method using long flip angle trains of
SNR priority VFA TSE flip angle schedules and PSF correction combined with
two-point Dixon fat suppression allows time-efficient large coverage peripheral
artery vessel wall MRI. Dixon VFA-TSE provides higher SNR, more uniform fat
suppression and better flow suppression than 3D-MERGE. Thus, Dixon VFA-TSE
method is a promising method for large coverage vessel wall imaging and may
find applications in abdominal and whole body VWI applications in addition to
femoral VWI.Acknowledgements
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