Simon Konstandin1 and Matthias Günther1,2
1MR-Imaging and Spectroscopy, University of Bremen, Bremen, Germany, 2Fraunhofer MEVIS, Bremen, Germany
Synopsis
Sodium MRI can act as a biomarker for heart tissue
viability. However, several aspects (blurring behavior of
non-Cartesian ultra-short echo time sequences, blurring because of heart motion,
small myocardial infarction (MI) regions) complicate MI detection due to
resolution reasons. Optimal sequence
parameters are difficult to find since many subject parameters (e.g.,
relaxation times, heart motion) must be considered. The presented
simulation model of a beating heart can be used to optimize sequence
parameters, among other things, for better visualization of MI and can be
adapted to any kind of motion and to different subject/physiological
parameters.Introduction
Sodium MRI can act as
a biomarker for heart tissue viability
1,2. As it suffers from low
signal-to-noise ratio (SNR), many techniques have been recently developed using
3D ultra-short echo time (UTE) sequences with anisotropic resolution and
retrospective electrocardiogram gating
3. In sodium heart MRI, several aspects (blurring
behavior of radial sequences, blurring because of heart motion, small myocardial infarction (MI) regions)
complicate MI detection due to resolution reasons. Optimal sequence parameters are difficult to find since many
subject parameters (e.g., relaxation times, heart motion) must be considered.
In this study, a beating heart was simulated to find optimal acquisition
parameters dependent on physiological parameters.
Methods
Simulations were performed
on an analytical heart model (short-axis) using Matlab (The MathWorks Inc.,
Natick, MA). The heart was modeled by ellipsoidal shapes only, since raw data
can be generated analytically4$$F(k_x,k_y,k_z)=\rho
abc\frac{\sin{(2\pi K)}-2\pi K\cos{(2\pi K)}}{2\pi^2K^3},$$with signal scaling
factor ρ, semi-principal axes of lengths a, b, c and$$K=\left((ak_x)^2+(bk_y)^2+(ck_z)^2\right)^{1/2}.$$Figure
1a shows the heart model with geometric dimensions and relative signal for
heart chambers (RV, LV), myocardium and assumed MI. A 3D density-adapted radial
UTE sequence3 was used for simulated acquisition with additional
complex pseudorandom Gaussian noise (Fig. 1b) with following parameters: 30,000
projections with golden angle distribution, 160 samples per projection, readout
time of 10 ms, in-plane resolution of 2.5 mm and anisotropy factor of 2 (i.e.,
5 mm). Data were averaged 10 times and regridded for a field-of-view of 300 mm
with a Kaiser-Bessel kernel5, oversampling ratio6 of
1.375 and iterative sample density estimation7. A scale factor
between 0.84 (maximum contraction) and 1.0 (diastole) for the heart dimensions was applied according to the function shown in Figure 1c to simulate heart
motion. A repetition time of 20 ms was used at a simulated random heartbeat of
55-65 min-1.
Simulations were
performed with different temporal window sizes (called assumed systole length), within which the projections were not
considered for reconstruction. In a second simulation, the resolution was continuously
reduced to consider signal loss because of fewer projections used. The
resolution was adapted to maintain SNR for increasing window sizes:$$\Delta x(w)=\left[\left(\frac{mCCL-w}{mCCL}\right)^{-1/2}\right]^{1/3}\cdot\Delta
x(w=0),$$where mCCL is the mean cardiac cycle length and w is the window length
of projections that are not considered for reconstruction.
Results
If all projections of
the heart cycle are considered for reconstruction, blurring due to heart motion
is clearly visible (Fig. 2a) compared to measurements at longer window sizes (Fig.
2b: 400 ms, Fig. 2c: 800 ms) with less motion/blurring. In Figure 2d, the
signal profile (dotted line in Fig. 2a) is shown for the three different window
sizes. It can be observed that the MI is better delineated at a window length
of 400 ms compared to 0 ms and 800 ms. More blurring occurs at signal
transitions if all projections are considered (black line). The SNR in the MI
region shows an optimum at about 380 ms assumed for the systole length (Fig.
2e). The same simulation was performed but the resolution was adapted for same
SNR values (Fig. 3). Maximum SNR in MI is obtained at a longer window size of
about 500 ms (Fig. 3e) compared to the former case.
Discussion & Conclusion
It could be demonstrated that sequence parameter
optimization is very important especially in case of any kind of motion. The
window length of retrospectively
chosen projections with golden angle increments and the resolution can be
optimized by the use of the presented beating heart model. Parameters like
relaxation times, heart motion, dimensions, etc. are considered. The
choice of the window length after heart contraction (in which projections are
not considered for reconstruction) is a trade-off between the proportions of motion
artifacts and SNR/resolution. In this study, an optimal window length could be
found for MI detection assuming a certain parameter set. Since resolution
cannot be changed (without modifying the readout time and SNR) after the
measurement, it is advisable to know optimal and SNR-efficient sequence parameters
by simulation of the actual parameter set. The main drawback of this study is that
heart motion is modeled only by a scale factor for the heart dimensions, whereas heart rotation and density changes are not considered. Future work should improve the heart model by
integrating a more realistic heart motion, which can be incorporated
after evaluation of a large cohort. Furthermore, other acquisition schemes (e.g.,
flexTPI8) should be investigated.
The presented simulation model of a beating
heart can be used to optimize sequence parameters, among other things, for
better visualization of MI and can be adapted to any kind of motion and to
different subject parameters.
Acknowledgements
No acknowledgement found.References
1. Boada FE, LaVerde G, Jungreis C et al. Loss of
cell homeostasis and cell viability in the brain: what sodium MRI can tell us.
Curr Top Dev Biol 2005;70:77-101.
2. Ouwerkerk R, Bottomley PA, Solaiyappan M et al.
Tissue sodium concentration in myocardial infarction in humans: a quantitative
23Na MR imaging study. Radiology 2008;248:88-96.
3. Konstandin S, Günther M. SNR-efficient anisotropic
3D ultra-short echo time sequence for sodium MRI with retrospective gating.
Proc Intl Soc Mag Reson Med 2015;2435.
4. Koay CG, Sarlls JE, Özarslan E. Three-dimensional
analytical magnetic resonance imaging phantom in the Fourier domain. Magn Reson
Med 2007;58:430-436.
5. Jackson JI, Meyer CH, Nishimura DG et al.
Selection of a convolution function for Fourier inversion using gridding. IEEE
Trans Med Imag 1991;10:473-478.
6. Beatty PJ, Nishimura DG, Pauly JM. Rapid gridding
reconstruction with a minimal oversampling ratio. IEEE Trans Med Imag
2005;24:799-808.
7. Zwart NR, Johnson KO, Pipe JG. Efficient sample
density estimation by combining gridding and an optimized kernel. Magn Reson
Med 2012;67:701-710.
8. Lu A, Atkinson IC, Claiborne TC et al. Quantitative sodium imaging
with a flexible twisted projection pulse sequence. Magn Reson Med
2010;63:1583-1593.