Carina Graf1 and Christopher T Rodgers2
1Wolfson Brain Imaging Centre, Department of Clinical Neuroscience, University of Cambridge, Cambridge, United Kingdom, 2University of Cambridge, Cambridge, United Kingdom
Synopsis
Keywords: Software Tools, Spectroscopy, non-cartesian MRSI
With the wider availability of ultra-high field MR systems,
metabolic imaging using MRSI is a fast-developing area of research. Frequently
used sequences use non-uniformly sampled trajectories to achieve
high-acceleration factors e.g. concentric-ring trajectories (CRT). In this
work, we demonstrate the from-scratch implementation of a simulation and reconstruction
tool for CRT-MRSI using (1) a regridding, (2) an iterative L2 linear solver as
well as (3) applying the non-uniform FFT implementation from the BART-toolbox to
simulated non-cartesian MRSI data with a known Fourier-transform pair. The
exact sampled data permits the evaluation of the impact of different reconstruction
implementations.
Introduction
Fast MRSI methods require high acceleration factors, in
comparison to traditional phase-encoded CSI. A common approach for high-resolution
MRSI is spatial-spectral sampling using non-cartesian trajectories1. These are advantageous over
cartesian trajectories due to the flexibility in balancing optimised sampling
pattern design with hardware constraints. A down-side of using non-uniform
sampling, however, is that the standard 2D Fast-Fourier Transform (FFT)
algorithm cannot be used for the solution of the inverse problem. Thus,
alternative reconstruction methods need to be applied to the sampled data.
There are generally two approaches for MRSI. (A) Gridding onto a cartesian grid
before performing the spatial 2D-FFT, followed by spectral processing and (B)
iterative optimisation of the inverse problem.
In this work, we implement a simple, from-scratch simulation
and reconstruction method which can be used for non-uniformly sampled k-space
trajectories. We demonstrate the usage on a set of concentric-ring trajectories (CRT) for a geometric spectroscopic phantom.Methods
k-space trajectories and definitions of an ellipsoid test
object were used to determine the non-uniformly sampled k-space samples. Since
the analytical Fourier of an ellipsoid is given by the Bessel functions of the
first kind J
1, exact k-space samples were determined for the given
test object. Spectral simulations included frequency modulation, magnitude
scaling and exponential T
2 decays.
Three approaches for the reconstruction of the non-uniformly
sampled data were implemented.
- Spatial
gridding with linear interpolation (“griddata”)
- Iterative
reconstruction using a L2 linear solver (“minres”)
- Iterative
reconstruction using the inverse nufft algorithm from the Berkeley Advanced
Reconstruction Toolbox (BART)2.
For the iterative reconstructions, the non-uniformly sampled
data set was first temporally Fourier-transformed followed by the spatial
iterative reconstruction of each individual frequency component.
The normalised root mean squared error (NRMSE) was
calculated for the quantitative analysis of the reconstructed MRSI compared to the
exact test object data.
All signal simulations and reconstructions were implemented
in MATLAB (R2021b, Mathworks).
Results
Figure 1 shows the workflow of the simulation tool
for the generation of exact non-cartesian sample data. This can be used on any
arbitrary k-trajectory, when a test object with an analytical Fourier transform
is equally sampled in the temporal domain.
The reconstruction implementation was demonstrated on five
distinct concentric-ring trajectories (Figure 2) highlighting different
aspects of CRT variations i.e. equidistant or density-weighted trajectories, as
well as the impact of sampling sparsity.
Reconstruction results for the three different methods are
shown in Figure 3. Note the distinct differences in scaling, and the impact of sparse sampling on the image reconstruction.
The NRMSE for each reconstruction approach is given in Table
1.Discussion & Conlcusion
We demonstrated a simulation and reconstruction tool for
non-cartesian MRSI which can be used on arbitrary sampling trajectories. Future
work may include simulation of imperfections including off-resonance effects
and gradient imperfections. The use of test objects which have an analytical
Fourier transform allows measuring the impact that different reconstruction
pipelines for non-cartesian data have as shown by comparing the three
reconstruction methods.
The simulation and reconstruction source code will be made
available on GitHub3.Acknowledgements
The Wolfson Brain Imaging Centre is supported by the NIHR
Cambridge Biomedical Research Centre and an MRC Clinical Research
Infrastructure Award for 7T research. CG is supported by a Cambridge European
Scholarship awarded by the Cambridge Trust and the W.D. Armstrong Studentship
in Engineering and Medicine. CTR is funded by the Wellcome Trust and the Royal
Society [098436/Z/12/B]. This work
was supported by Innovate UK [10032205] under the Guarantee Scheme relating to
the EU Horizon Europe project MITI [101058229] and European Union’s
H2020 research and innovation program under grant agreement [801075].References
1. Bogner W,
Otazo R, Henning A. Accelerated MR spectroscopic imaging-a review of current
and emerging techniques. NMR Biomed. John Wiley and Sons Ltd;
2020;2020/05/14:e4314.
2. Martin Uecker, Frank Ong, Jonathan
I Tamir, Dara Bahri, Patrick Virtue, Joseph Y Cheng, Tao Zhang, and
Michael Lustig. Berkeley
Advanced Reconstruction Toolbox. Annual Meeting ISMRM,
Toronto 2015, In Proc. Intl. Soc. Mag. Reson. Med. 23:2486
3. https://github.com/brainchemie/non-uniform_MRSI_Reconstruction.git