Renata Porciuncula Baptista1, Alexandre Vignaud1, Chaithya G R1,2, Guillaume Daval-Frérot1,2, Franck Mauconduit1, Mathieu Naudin3, Marc Lapert4, Remy Guillevin3, Philippe Ciuciu1,2, Cécile Rabrait-Lerman1, and Fawzi Boumezbeur1
1NeuroSpin, Joliot, CEA, CNRS, University Paris-Saclay, Gif-sur-Yvette, France, 2Inria, Parietal, Université Paris-Saclay, Palaiseau, France, 3University Hospital Centre Poitiers, DACTIM-MIS, Poitiers, France, 4Siemens Healthcare SAS, Saint-Denis, France
Synopsis
Quantitative 23Na MRI provides useful information about brain tissue homeostasis. Most sequences use deterministic non-Cartesian 3D trajectories such as TPI. However, stochastic strategies such as SPARKLING could improve the coverage of k-space. This study evaluates the advantages of SPARKLING versus TPI. From in vivo datasets at 7T, we determined that undersampled SPARKLING acquisitions outperform TPI for (8 mm)3 resolution with a birdcage coil or for (4 mm)3 with a 32-channel coil. Through extrapolation of these results, we predict that at 11.7T/32-channel, 23Na MRI data could be acquired in 90s at (3 mm)3, which could be interesting for sodium fMRI imaging.
Introduction
Sodium (23Na) MRI in the human brain provides unique information about physiology in vivo. Several studies confirmed the relevance of assessing total sodium concentration in different neurological diseases such as Alzheimers1 and Multiple Sclerosis2. Current studies use ultra-short echo time (UTE) sequences combined with deterministic non-Cartesian k-space trajectories such as radial, TPI3 or FLORET4. Still, acquisition times (TA) remains relatively long even at high magnetic field due to the moderate intrinsic NMR sensitivity of sodium and its low concentration. Although more efficient than Cartesian trajectories, these standard non-Cartesian readouts do not fully cover the k-space as they are analytically and thus geometrically constrained. Therefore, we assume that X-nuclei MRI in general and 23Na MRI acquisitions in particular could benefit from optimization-driven compressed-sensing (CS) approaches5 like SPARKLING6,7 that end up with (i) global variable density sampling but (ii) locally uniform coverage of k-space. As preliminary shown in SWI, this approach is good candidate to to shorten the TA without degrading image quality in 23Na MRI. Determination of scenarios of interest is not trivial because CS performance depends on signal-to-noise ratio (SNR) and image sizes8. In this study, our goal is to identify the best combination of undersampling and input SNR (i.e. voxel size) for which SPARKLING outperforms TPI.Material and Methods
For both in vivo and in vitro, 3D radial UTE at (8 mm)3 with a number of
shots (Ns$$$=4\pi(k_{max}FOV)^2$$$) chosen to
meet Nyquist criteria9 and a number of 32 averages (NA)
were used as reference image for our simulations. This
study explores different acceleration factors ($$$\textit{AF}=\dfrac{N_s\textit{radial full nyquist}}{N_s\textit{current acquisition} }$$$) and resolutions and focus on a fixed set of parameters: TR/TE=20/0.5
ms, FA=55°, FOV = (240 mm)3, dwell time = 10 us, 1248 points, which
has previously been optimized for in vivo
23Na MRI acquisition10.
MRI data were
acquired on Magnetom or Terra 7T MR Siemens scanners (Siemens Healthineers)
using respectively a dual-resonance 1H/23Na birdcage or a
32-channel coil (Rapid Biomedical).
Input
SNR per spoke was measured from these experiments. Gaussian noise was added to the reference complex k-space data to simulate the
performances of SPARKLING and TPI strategies (Fig.1) at lower input SNR. For
each considered input SNR, k-space was subsampled at
various AF (2, 4, 16, 32,
64, 128).
Images were
reconstructed CS reconstruction with density compensation11 using
Pysap-MRI12-13, which handles large 3D non-Cartesian multichannel
datasets. For each reconstruction, the regularization parameter6
(lambda) was chosen visually in the 10-7 to 10-20 range
(30 steps) to maximize image quality.
The metric chosen
for comparison was the SSIM14 score which attempts to model and
mimic the human visual system.
In order to
validate our simulations, in vitro
sodium images of a homemade phantom were acquired using both TPI and SPARKLING
sampling schemes using the same acquisition parameters for a resolution of (8 mm)3 and NA=32. Separate datasets were acquired at AF=2, 4, 16, 32, 64,
128.
Once
our simulations were validated in vitro
(Fig.2), in vivo 23Na MRI datasets were acquired in one human volunteer
at AF=2, 4, 32, 64, 128. Resolution and NA were set to
match SNR used successfully in the simulations while keeping the total
examination time below 60 minutes.
In vivo 23Na
images acquired with the 32-channel coil exhibited an improved SNR compared to
the birdcage coil. Input SNR expected at 9.4 and 11.7T were extrapolated
considering the relationship $$$\dfrac{SNR_ {target}}{SNR_{7T}}=\left(\dfrac{B_0}{7}\right)^{1.65}$$$15.
Results
Figure 2 plots the SSIM scores obtained for each AF and shows a fair agreement between the simulations and phantom data. Figures 3 and 4 display respectively our in vitro and in vivo experimental data along the corresponding simulations. SPARKLING outperform TPI for 23Na MRI data acquired at (8 mm)3 resolution especially for larger AF. In particular, we could obtain similar image qualities for TPI at AF=2 and SPARKLING at AF=32 thus 16-fold faster acquisition. Figure 5 shows the comparison between TPI and SPARKLING at (4 mm)3 resolution with a 32-channel coil showing similar results for TPI at AF=8 and SPARKLING at AF=32.Discussion
As illustrated,
we obtained an overall good agreement between our experimental and simulated results.
Residual differences could be attributed to slight differences in the
point-spread-functions, in particular due to T2*-weighting.
SSIM is known to be is weakly sensitive to blurring16. In both in vitro and in vivo results, SPARKLING results resist to
higher acceleration factors compared to TPI images.
However, a minimum input SNR value has to be reached to see this effect. For
lower magnetic fields or coils sensitivity, TPI as well as other deterministic
k-space non-Cartesian trajectories stay relevant. Conclusion
At 7T with a
birdcage coil, center-out 3D SPARKLING undersealing scheme outperforms TPI for 23Na
MRI at (8 mm)3 resolution. This advantage is particularly
predominant for AF>8. At 7T with a 32-channel coil for a (4 mm)3 resolution,
32-fold accelerated SPARKLING provides similar results to 8-fold accelerated
TPI. Based on our simulation extrapolating the input SNR for 23Na
MRI at 11.7T, we expect to acquire dynamic sodium MRI within 90 seconds with a (3
mm)3 resolution, which could be of interest to revisit sodium
changes during neuronal activation as proposed by Bydder et al17. Acknowledgements
This work received financial support from Leducq Foundation (large equipment ERPT program, NEUROVASC7T project. Chaithya G R was supported by the CEA NUMERICS program, which has received funding from the European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant agreement No 800945. This work was granted access to the HPC resources of IDRIS under the allocation 2021-AD011011153 made by GENCI.References
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