Thomas Hüfken1, Fabian Bschorr1, and Volker Rasche1
1Ulm University, Ulm, Germany
Synopsis
Keywords: Artifacts, Artifacts
Motivation: Effect of free diffusion introduced image blur is well known but measurable samples always have solid boundaries which results in non-blur like artefacts in ultra-high-resolution images.
Goal(s): Demonstration of diffusion introduced artefact behavior near impermeable barriers.
Approach: A Monte Carlo simulation of particles undergoing a random walk was performed and CTI specific point spread functions (PSFs) and 1D images determined.
Results: It was demonstrated that the PSF yields asymmetric blur and signal enhancement in direct vicinity of the barrier. Simulations clearly indicating the PSF to be dependent on spatial resolution and gradient strength.
Impact: These
results will help to prohibit misinterpretation of MR images of small structures
with ultra-high-resolution MRI.
Introduction
Constant Time Imaging (CTI)1 has
previously demonstrated its capacity to produce images with an isotropic
resolution of (3µm)³. However, spatial resolution in the µm range is primarily
hindered by two factors: signal-to-noise ratio (SNR) and diffusion effects.
While the deficiency in SNR can be addressed through techniques such as signal
averaging or hardware enhancements, diffusion-induced image distortions can be
managed by employing high gradients. It is widely accepted that the impact of
free diffusion can be represented in a Point Spread Function (PSF)2,3,4.
This study investigates the effect of diffusion hindering barriers on the PSF.
To this end, random walks of numerous particles influenced by an impermeable
barrier were simulated, and the corresponding PSFs and images were determined.Methods
The CTI
sequence is composed of an excitation pulse, succeeded by a phase encoding
gradient. This gradient is presumed to be rectangular with an amplitude $$$G_{max}$$$
and duration $$$t_{enc}$$$. This is followed by data acquisition.
Monte Carlo
simulations were employed to calculate the random walks, utilizing MATLAB
2021b (MathWorks,Natick,MA,USA). For each step time $$$Δt$$$ of the random
walks, the spins’ displacements are $$$Δr$$$ in a random direction
$$$|Δr|=\sqrt{6D_{free}Δt}$$$ with a diffusion coefficient $$$D_{free}=2\cdot10^{-9}m^2/s$$$ 5.
The number of diffusion particles was experimentally chosen to be 50,000, as
well as 1,000 time steps that defined the step time $$$Δt=t_{enc}/1000$$$. The phase
added to a particle at position $$$x$$$ for a single time step is $$$Δφ=γGxΔt$$$. The
contribution of one particle to the signal at the end of encoding is the cosine
of its final phase. The measurable signal is equal to the sum of signals from all
particles.
The
computation of measurable signal was re-iterated for different gradient
strengths to completely fill k-space (figure 1).
The presence of a barrier was accounted for by defining an area
with $$$x>0$$$ where particles are not permitted. If an iteration results in
particles in the restricted area, the step is repeated for those specific
particles6,7.
For the
calculation of diffusion-impacted PSFs, all particles are initially
positioned at the origin at $$$t=0$$$. For one-dimensional imaging, particles were
evenly distributed along the line $$$y=z=0$$$, starting from the origin to -40% of
the FOV (figure 4).
For
comparison purposes, analytical PSFs were computed based on A.G. Webb’s
publication, considering both, free diffusion and sampling.Results
Figure 2 depicts the results of the random walk simulated
(orange stars) with analytically determinable PSFs (blue line) at 5 and 1µm
spatial resolution. Maximum gradient amplitude was chosen as 1T/m.
Figure 3 shows simulation results for PSFs under the
influence of an impermeable barrier with resolutions of 5 and 1µm,
respectively.
Simulated
1D images are shown in figure 5 for varying
gradient strengths of 0.1, 0.5 and 1T/m at a constant resolution of 5µm, and
varying spatial resolution of 1, 3 and 5µm at constant gradient strength of
1T/m.Discussion
The data
presented in figure 2 indicates a strong
correlation between the simulation and the theoretical PSF3. The
minor misalignment observed at the minima adjacent to the global maximum for
the 5µm resolution can be attributed to the finite number of particles utilized
in the simulation.
Simulated
PSFs depicted in figure 3 show an almost
symmetric shape for 5µm resolution that is comparable to unrestricted diffusion
(figure 2). However, for 1µm resolution the PSF results
highly asymmetric and the FWHM becomes smaller. This clearly shows the
increasing impact of the barrier with decreasing spatial pixel size at constant
gradient strength.
The residual
noise-like ripples on the plateaus (figure 5) is
most likely caused by the limited number of particles. An obvious difference in
the image blur between the unrestricted (left) and restricted diffusion (right
side of object) can be observed. Where in case of unrestricted diffusion the
expected image blur can be observed in case of restricted diffusion a clear
signal increase with decreasing distance to the barrier occurs. The signal
increase depends on gradient strength and spatial resolution. This effect is
new and has not be shown in other related or recent work like 1,2,3,4Conclusion
This work
can help to prohibit misinterpretation of MR images of small structures
especially with the ongoing development in high resolution MRI. It examined
that in the direct vicinity of an impermeable barrier, the impact of diffusion
on CTI causes signal increase. The amplitude, as well
as the width of this artefact increases with smaller spatial dimensions of
pixels and lower gradient amplitudes. This effect has to be considered for
final image interpretation of high-resolution MRI.Acknowledgements
The authors thank the Ulm University Center for Translational Imaging MoMAN for its support.References
1: WEIGER, Markus, et al. NMR microscopy with isotropic resolution of 3.0 μm using dedicated hardware and
optimized methods. Concepts in Magnetic Resonance Part B: Magnetic Resonance
Engineering: An Educational Journal, 2008, 33. Jg., Nr. 2, S. 84-93.
2: CALLAGHAN,
P. T.; ECCLES, C. D. Diffusion-limited resolution in nuclear magnetic resonance
microscopy. Journal of Magnetic Resonance (1969), 1988, 78. Jg., Nr. 1,
S. 1-8.
3: WEBB, A.
G. Optimizing the point spread function in phase‐encoded magnetic resonance
microscopy. Concepts in Magnetic Resonance Part A: An Educational Journal,
2004, 22. Jg., Nr. 1, S. 25-36.
4: GRAVINA,
Samuel; CORY, D. G. Sensitivity and resolution of constant-time imaging. Journal
of Magnetic Resonance, Series B, 1994, 104. Jg., Nr. 1, S. 53-61.
5: HOLZ, Manfred; HEIL, Stefan R.; SACCO, Antonio. Temperature-dependent self-diffusion
coefficients of water and six selected molecular liquids for calibration in
accurate 1H NMR PFG measurements. Physical Chemistry Chemical Physics,
2000, 2. Jg., Nr. 20, S. 4740-4742.
6: GILANI,
Nima; MALCOLM, Paul; JOHNSON, Glyn. An improved model for prostate diffusion
incorporating the results of Monte Carlo simulations of diffusion in the
cellular compartment. NMR in Biomedicine, 2017, 30. Jg., Nr. 12, S. e3782.
7: GILANI,
Nima; MALCOLM, Paul; JOHNSON, Glyn. A monte carlo study of restricted
diffusion: Implications for diffusion MRI of prostate cancer. Magnetic
Resonance in Medicine, 2017, 77. Jg., Nr. 4, S. 1671-1677.