Praveen Iyyappan Valsala1, Philipp Ehses2, Marten Veldmann2, and Klaus Scheffler1,3
1Magnetic Resonance Center, Max-Planck Institute for Biological Cybernetics, Tübingen, Germany, 2German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany, 3Department of Biomedical Magnetic Resonance, Eberhard Karls University Tübingen, Tübingen, Germany
Synopsis
We investigate the possibility of using longer multi-shot spiral readouts to accelerate balanced steady-state free precession (bSSFP) at ultra-high field (UHF) for functional imaging. The reconstruction is performed with the full signal model accounting for spatial B0 inhomogeneity and gradient imperfections. We present the activation maps from flickering checkerboard stimulus experiment and discuss challenges of spiral bSSFP at UHF.
Introduction
The BOLD (blood oxygen level dependent) signal of bSSFP sequences is believed to be more localized to the site of neuronal activation because of its higher specificity to smaller vessels1 compared to standard gradient-echo EPI. In addition, the higher BOLD effect and higher SNR at high fields could be used to partially compensate for the loss in sensitivity of the bSSFP technique. These considerations motivate the investigation of bSSFP BOLD at higher fields2. However, the acquisition speed of the conventional Cartesian bSSFP methods is significantly lower than EPI. A Highly segmented echo planar readout with longer TR was proposed for improving the readout efficiency3,4. To further speed up the acquisition, this work looks into the feasibility of a multi-shot spiral bSSFP readout15 for fMRI application at UHF.Methods
Paradigm and fMRI Analysis: An alternating radial checkerboard pattern covering the full visual field is used. The block design consists of equal rest and stimulation duration of 14 s each and 240 volumes were acquired in 5.6 minutes.
We used the FSL FEAT package with recommended settings for functional analysis5. A general linear model fitting is used after temporal filtering (30s high pass) with a gamma hemodynamic response function and its temporal derivative as explanatory variables.
Sequence: A highly segmented 3D stack-of-spirals sequence with multiple interleaves is used. The uniform density Archimedean spiral-out trajectory is calculated at the scanner using a time-optimal algorithm6.
Acquisition: Passband bSSFP spiral dataset with TR/TE=10/2 ms, FOV = 192x192x20 mm3, matrix size = 192x192x20 and flip angle= 15 deg is acquired. After in-plane acceleration of R=3, 7x20 spiral acquisitions of about 5.4 ms each are collected which gives a volume TR of 1.4 s. A low resolution triple echo GRE scan is performed to obtain coil sensitivity and spatial B0 field maps. To allow for the correction of gradient imperfections, the gradient impulse response function (GIRF)7 is measured using a 16 channel 19F-NMR field probe system8. All experiments were performed with a human 9.4T scanner (Siemens Healthineers, Erlangen, Germany).
Reconstruction: After retrospectively correcting the trajectory deviations with the measured GIRF, an iterative cg-SENSE reconstruction is performed with NUFFT9 and multi-frequency interpolation (MFI)10 of spatial B0 effects for computational efficiency. The encoding model is preconditioned with the density compensation function (DCF) to reduce the number of iterations required for convergence11. The coil sensitivity maps are calculated using the ESPIRiT method12 of the BART toolbox. The temporal unwarp algorithm called UMPIRE13 followed by denoising by regularized fieldmap estimation14 are used for a robust spatial B0 map computation.Results
In figure 2, we show the improved image quality of the cg-SENSE reconstruction with B0 correction. Although, the spiral readout was relatively short (~5.4 ms), the spatial B0 inhomogeneity of approximately 200 Hz within the brain results in significant blurring. The tSNR (temporal SNR) analysis in figure 3 shows tSNR values in the range of 15-20 with significantly lower values close to banding artifacts. The spatial B0 correction appreciably increases tSNR across all slices. Even with the sub-optimal experimental condition, the results of our fMRI analysis show considerable positive and negative activations (see Figure 4).Discussion
With a non-optimized ADC duty cycle of 54% and the higher efficiency of spiral readout, we already surpassed the acquisition speed of SE-EPI at lower field4. The major hurdle in sustaining and improving the acquisition speed of bSSFP methods is controlling the spatial B0 inhomogeneity. Some existing solutions to this problem employ advanced shimming techniques or use a phase offset to move the low signal region away from the region of interest when full coverage is not required. Alternatively, phase-cycled bSFFP could be used for full coverage at the cost of spatio-temporal resolution.
As the sequence was already operating close to the SAR limit with a flip angle of 15 degrees, no explicit fat suppression was used in the experiment. However, we inverted the slice gradient polarity to move the chemical shift artifact to the top of the acquired volume, so that it shows up as a ring outside of the brain.Conclusion
The 3D stack-of-spiral acquisition holds potential to enable
and accelerate distortion-free accurate functional imaging at UHF with high
spatial specificity.Acknowledgements
The financial support of Max-Planck society is gratefully
acknowledged.References
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