A Beating Heart Simulation for Sequence Optimization of Sodium MRI
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 viability1,2. 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 gating3. 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.

Figures

FIG. 1. a: Heart model with geometric dimensions and relative signal for heart chambers (RV, LV), myocardium and assumed myocardial infarction (MI). b: Simulated 3D radial UTE acquisition with projections distribution based on the golden ratio. c: Geometric scale factor for heart dimensions to simulate heart motion.

FIG. 2. a-c: Simulated acquisition with different temporal window sizes, within which the projections were not considered for reconstruction. d: Signal profile (dotted line in a) to show the detectability of the myocardial infarction (MI). e: SNR of the MI in dependence of the assumed systole length.

FIG. 3. a-c: Simulated resolution-adapted acquisition with different temporal window sizes, within which the projections were not considered for reconstruction. d: Signal profile (dotted line in a) to show the detectability of the myocardial infarction (MI). e: SNR of the MI in dependence of the assumed systole length.



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
3943