Matthias Schloegl1, Stefan Spann1, Christoph Aigner1, Martin Holler2, Kristian Bredies2, and Rudolf Stollberger1
1Institute of Medical Engineering, Graz University of Technology, Graz, Austria, 2Institute of Mathematics and Scientific Computing, University of Graz, Austria
Synopsis
Dynamic arterial spin labeling MRI provides important quantitative
information about blood arrival time and perfusion. However, the
inherently low signal-to-noise ratio requires repeated measurements
to achieve a reasonable image quality. This leads to long acquisition
times and hence increases the risk of motion artifacts, which impedes
clinical applicability. To overcome this limitation we propose to
reconstruct the dynamic ASL data employing ICTGV regularization from
a reduced number of averages. The performance of the method is
evaluated on synthetic and in-vivo ASL data.
INTRODUCTION
Dynamic arterial spin
labeling MRI provides important quantitative information about blood
arrival time and perfusion, by measuring the difference between
control (C ) and spin-labeled (L) data for
multiple post-labeling delays. However, due to an inherently low
signal-to-noise ratio of the difference between C and L, repeated
measurements are required to achieve a reasonable image quality. This
leads to long acquisition times and hence increases the risk of
motion artifacts, which impedes clinical applicability. To overcome
this limitation we propose to reconstruct the
dynamic ASL data employing ICTGV regularization1 from a reduced
number of averages. ICTGV proved to be a suitable regularization
functional to stabilize reconstruction from highly undersampled
dynamic MRI applications and is therefore expected to allow a
suppression of noise in dynamic ASL. The performance of the proposed
approach is evaluated on synthetic and in-vivo ASL data.METHODS
For baseline evaluation a numerical phantom was generated based on a
high-resolution T1w-MRI of our database. The phantom was computed
using Matlab and SPM12 as described in Zhao et al.2 MRI
rawdata was simulated with 20 artificial receiver-coil sensitivities
and different noise-levels. In-vivo ASL data was acquired from one
subject using FAIR-QII with a 3D-GRASE readout.3 The
following acquisition parameters were used on a clinical 3T system: TR/TE = 2500/20ms, matrix
64x64, voxel size 3x3x3mm³, 30 slices, 6 segments, Turbo-factor =
15, EPI-factor = 21, 9 post-labeling delays: TI1,1 / TI1,2 / TI1,{3-9} = 300 / 600 / 800, TIfirst/ ΔTI /TIlast = 500 / 250 / 2500 ms. 7 averages for
each TI were acquired resulting in a total acquisition time of
approximately 33min.
Reconstructions were
computed with ICTGV regularization usging the AVIONIC framework
(https://github.com/IMTtugraz/AVIONIC),
from the different noise-levels of the synthetic phantom as well as
for seven to one averages from in-vivo data.RESULTS
Figure 1 displays the
recovery of noisy phantom data by means of ICTGV reconstruction for
realistic, linearly increasing noise levels for different
post-labeling delays. Figure 2 shows
results from invivo data, similar as in Figure 1, but with recovery
from different amounts of averages avg=(7,5,3,1) comparing to
non-denoised data. The corresponding series of all post-labeling
delays for selected voxels comparing gold-standard 7fold averaging, non-averaged ICTGV reconstruction and conventional reconstruction, resp., is displayed in Figure 3.DISCUSSION AND CONCLUSION
The results
demonstrate that a substantial suppression of noise can be achieved
using the proposed regularization approach. This is accomplished by
taking into account correlations of the varying signal intensity
along the marked post-labeling delays. Image quality can be achieved with ICTGV reconstruction from non-averaged
data, as with seven-fold averaging.
This reduces the scanning time from 33min to 4min 45s.
This improvement potentially helps to enable the
consolidation of clinical applicability and higher spatial
resolutions. Further improvements with this method may be achieved by
computing reconstructions from the 3D-parametric data, which was
processed slice-by-slice in this work to reduce the
computational burden. The implementation as well as comparison to
state-of-the-art methods will be subject to future work.Acknowledgements
BioTechMed-Graz
Funded by the
Austrian Science Fund (FWF) SFB-F3209-18
NVIDIA
Corporation Hardware grant support
References
1.
Schloegl M, Holler M, Bredies K, et al. Infimal convolution of total
generalized variation functionals for dynamic MRI. Magnetic Resonance
in Med. 2016; doi:10.1002/mrm.26352
2.
Zhao L, Fiedlden SW, Feng X, et al. Rapid 3D dynamic arterial spin
labeling with a sparse model-based image reconstruction. Neuroimage
2015;121:205-216
3.
Günther
M,
Oshio
K,
Feinberg
DA.
Single-shot 3D imaging techniques improve arterial spin labeling
perfusion measurements. Magn
Reson Med.
2005;54(2):491-498