Volkert Roeloffs1, Nick Scholand1,2, and Martin Uecker1,2,3
1Institute for Diagnostic and Interventional Radiology, University Medical Center Göttingen, Goettingen, Germany, 2DZHK (German Centre for Cardiovascular Research), Partner Site Göttingen, Germany, Goettingen, Germany, 3Campus Institute Data Science (CIDAS), University of Göttingen, Göttingen, Germany, Goettingen, Germany
Synopsis
Sensitivity to T1 and T2 in frequency-modulated SSFP sequences can be
increased by choosing a higher modulation speed without prolonging the
repetition time. In this work, we assess the boost in sensitivity by
Cramér-Rao-bound analysis, combine the sequence with stack-of-stars
sampling and subspace-constrained reconstruction, and demonstrate joint
T1/T2/B1/off-resonance mapping in phantom and in vivo study. The results
render fast-sweep frequency-modulated SSFP an excellent candidate for
comprehensive 3D multi-parametric mapping.
INTRODUCTION
Recently, phase-cycled bSSFP methods were proposed to achieve robust joint
T1/T2 mapping [1, 2]. These methods acquire a set of bSSFP images at
different transmitter frequencies to jointly estimate parameter maps and
off-resonance distribution. An alternative to the subsequent preparation of
different steady states is given by frequency-modulated SSFP (fmSSFP), a bSSFP
sequence in which the transmitter frequency is modulated slowly but continuously
[3]. While a very slow modulation ("quasistatic") simply sweeps through
the classic bSSFP spectrum, a faster modulation results in a different signal
response.
In this work, we investigate the increased sensitivity of the
"fast-sweep" fmSSFP, combine this novel sequence with a stack-of-stars sampling
scheme, and demonstrate joint T1/T2/B1/off-resonance mapping in phantom and in
vivo.THEORY
To investigate the effect of changing the modulation or sweeping speed in
an fmSSFP sequence, we simulate a conventional bSSFP signal response using
the Bloch equations where the transmitter phase of the nnn-th pulse is
modulated according to
$$\phi(n)= 180^\circ n + 360^\circ \frac{n^2}{2P}$$
where $$$P$$$ is the period of the generated signal and controls the
sweeping speed. Two representative signal time courses are shown in Fig.
1 with periods $$$P$$$=50000 (slow sweep, left column) and $$$P$$$=1616 (fast
sweep, right column). To assess the sensitivity of the respective Bloch
responses, a relative Cramér-Rao-bound (rCRB) analysis was performed similar to
[4]:
$$ \text{rCRB(}M_0\text{)} = \sigma^{-2} T_\text{exp} \left[I^{-1}(\theta)\right]_{11} $$
$$ \text{rCRB(}R_1\text{)} = \sigma^{-2} R^2_1 T_\text{exp} \left[I^{-1}(\theta)\right]_{22} $$
$$ \text{rCRB(}R_2\text{)} = \sigma^{-2} R^2_2 T_\text{exp} \left[I^{-1}(\theta)\right]_{33} $$
with noise variance $$$\sigma^2$$$, Fisher-Information matrix
$$$I(\theta)=\sigma^{-2}(DS)^{H}(DS)$$$, total duration of the sweep
$$$T_\text{exp}$$$, and Jacobi matrix of the signal $$$DS$$$.
By increasing
the modulation speed of the fmSSFP signal, the sensitivities of both T1
and T2 can be increased as relaxation effects are introduced into the
signal time course, resulting in asymmetries that decouple the partial
derivatives of R1 and R2 (Fig. 1).METHODS
A 3D stack-of-stars trajectory is combined with a frequency-modulated SSFP
sequence. Partitions are sampled in the innermost loop and Tiny-Golden-Angle
sampling [5] is performed within each partition. All partitions are aligned to
allow simple decoupling by inverse FFT prior to reconstruction.
Image
reconstruction is performed in the low-frequency Fourier subspace as detailed
in [6,7] using BART [8] utilizing coil estimation by ESPIRIT [9] and gradient
delay correction with RING [10].
For fast-sweep fmSSFP, in contrast to phase-cycled bSSFP, no closed-form
signal models are available so far. Therefore, we modeled the signal time
course within the framework of Extended Phase Graphs (EPG, [11]) and projected
to the low-frequency Fourier subspace subsequently.
The presented approach was validated in a phantom study (NIST system
standard model 130, TR=5.0 ms, FA=15°, 1×1×3 mm3, 1616 spokes per
partition, 32 partitions, $$$P$$$=1616, 1616 prep. pulses,
$$$T_\text{ACQ}$$$=4m20s) and in a volunteer without known illness (same
acquisition parameters).RESULTS
Figure 2 shows the parameter maps obtained after pixelwise fitting of the
EPG signal model to the complex-valued subspace coefficients (exemplary
slice). A ROI-based comparison with a gold standard T1 and T2 measurement
(multiple inversion FLASH and single-echo spin echo) reveals good
accuracy.
Figure 3 shows reconstructed subspace coefficient maps, fitting results
and fit residuals for the brain study. Fitting accuracy is excellent
except for regions with subcutaneous fat or flowing CSF.
A synthesized time series can be computed from the reconstructed subspace
coefficient maps and is shown in Figure 4.
Figure 5 shows parameter maps of the brain study similar to Fig 2.
A ROI-based analysis for white and gray matter showed good agreement for
both T1 and T2 with literature findings [12,13]. Similar to the phantom
study, a coupling between M0 and relative B1 can be observed.DISCUSSION & CONCLUSION
In this work, we demonstrated that fmSSFP can be sensitized to T1 and T2
by increasing the modulation speed. The reason for this effect might lie in the
fact that for a slow or "quasistatic" modulation, the system stays in
a memoryless steady state while a fast sweep introduces relaxation effects that
depend on the state at previous time points. This signal behaviour enables
decoupling of T1 and T2 dependencies without increasing the repetition time
as suggested in [14].
Several properties render this sequence very attractive for 3D
multi-parametric mapping, which are a) continuous data acquisition without
intermediate preparation phases, b) off-resonance-resolved reconstruction,
and c) availability of a subspace model.
Initial results are promising and we believe fast-sweep fmSSFP to be an
excellent candidate for fast and comprehensive multi-parametric mapping.
As a next step, the observed coupling between $$$M_0$$$ and relative $$$B_1$$$
needs to be analyzed and eventually overcome.
A future integration of this signal model into a non-linear model-based
reconstruction could help to better decouple individual parameter maps (e.g. $$$M_0$$$
from relative $$$B_1$$$) by incorporating prior knowledge and advanced
regularization.Acknowledgements
Supported by the DZHK (German Centre for Cardiovascular Research)References
[1] Nguyen et al., "MIRACLE: Motion-Insensitive RApid Configuration
ReLaxomEtry", JMRI 36.4 (2012)
[2] Shcherbakova et al., "PLANET: an ellipse fitting approach for
simultaneous T1 and T2 mapping using phase‐cycled balanced steady‐state
free precession." MRM 79.2 (2018)
[3] Foxall et al., "Frequency‐modulated steady‐state free precession
imaging", MRM 48.3 (2002)
[4] Assländer et al., "Optimized quantification of spin relaxation times
in the hybrid state" MRM 82.4 (2019)
[5] Wundrak et al., "Golden ratio sparse MRI using tiny golden angles."
MRM 75.6 (2016)
[6] Roeloffs et al., "Frequency‐modulated SSFP with radial sampling and
subspace reconstruction: A time‐efficient alternative to phase‐cycled
bSSFP." MRM 81.3 (2019)
[7] Roeloffs et al., "Joint T1/T2 mapping with frequency-modulated SSFP,
radial sampling, and subspace reconstruction.", Proc. ISMRM 2018, 3702
[8] BART 0.6.00 Toolbox for Computational Magnetic Resonance Imaging, DOI:
10.5281/zenodo.3934312
[9] Uecker et al.. "ESPIRiT—an eigenvalue approach to autocalibrating parallel
MRI: where SENSE meets GRAPPA", MRM 71.3 (2014)
[10] Rosenzweig et al., "Simple auto‐calibrated gradient delay estimation from
few spokes using Radial Intersections (RING).", MRM 81.3 (2019)
[11] Hennig et al., "Echoes—how to generate, recognize, use or avoid them
in MR‐imaging sequences. Part I: Fundamental and not so fundamental
properties of spin echoes" Concepts in Magnetic Resonance 3.3 (1991)
[12] Gelman et al., "MR imaging of human brain at 3.0 T: preliminary
report on transverse relaxation rates and relation to estimated iron
content.", Radiology 210.3 (1999)
[13] Ethofer, et al. "Comparison of longitudinal metabolite
relaxation times in different regions of the human brain at 1.5 and
3 Tesla.", MRM 50.6 (2003)
[14] Shcherbakova et al., "On the accuracy and precision of PLANET for
multiparametric MRI using phase‐cycled bSSFP imaging", MRM 81.3 (2019)