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Efficient correction for MRI artifacts due to nonlinear variations in magnetic field using principal component analysis
Daniel I Gendin1 and Jiaen Liu2
1Advanced Imaging Research Center, UT Southwestern Medical Center, Dallas, TX, United States, 2Advanced Imaging Research Center and Radiology, UT Southwestern Medical Center, Dallas, TX, United States

Synopsis

Keywords: Image Reconstruction, Brain

Head motion can lead to artifacts in MR images. One source of motion artifacts is dynamic nonlinear variation in the background magnetic field (B0). Fully accounting for this variation is computationally intractable. We proposed an efficient method of performing this correction by making use of principal component analysis and considering only a few dominant modes. We applied our method to measured data and compared the results to the case with no correction as well correction using a previous K-means based method.

Introduction

MRI is prone to motion-induced artifacts. One potential source for these artifacts is the fact that head motion can lead to spatially nonlinear dynamic changes in the background polarizing magnetic field (B0) due to the static B0 shim setting and motion-induced spatial changes of magnetic susceptibility in the head and torso1. The resulting artifacts become much more pronounced at higher field strengths (e.g. 7T) and in methods focusing on the susceptibility effect such as T2*-weighted MRI. Therefore, in order to fully take advantage of high-field MRI’s unique ability to image fine scale structures, the effect of motion-induced nonlinear B0 fluctuation must be corrected for. Several works have attempted to address this issue2-4. Performing the correction on a shot-by-shot basis is computationally expensive. Here, we proposed an efficient method based on principal component analysis (PCA) of the B0 effect on MRI signal5 and compared with another method using K-means clustering4.

Methods

Principle of PCA-based B0 correction
The forward equation for how MR signal is affected by the B0 field (unit hertz) is:
$$s(k(t))=M\cdot\mathcal{FT}\{e^{2i\pi\,TE\,B_0(r,t)}\rho(r)\}.$$
Here, $$$s$$$ is the signal, $$$\rho$$$ is the underlying image, $$$TE$$$ is the echo time, $$$\mathcal{FT}$$$ is the Fourier transform, and $$$M$$$ is the motion operator (for simplicity, B1 sensitivity is omitted here). Directly solving this equation would require as many FTs as there are B0 measurements, which is computationally intractable. To efficiently perform the correction, we approximated the exponential phase factor (EPF) from the equation above with a sum of a few principal components (as proposed by Wilm et. al5).
$$\text{EPF}=e^{2i\pi\,TE\,B_0(r,t)}\approx\sum_{j=1}^Lb_j(r)c_j(t).$$
Here, $$$b_j(r)$$$ is the jth principal mode or component, $$$c_j(t)$$$ is the weight of mode j at time t, and $$$L$$$ is the number of components that was used to perform the approximation.
Example values of the EPF and its corresponding principal modes are presented in Figure 1.
Plugging this decomposition into the forward equation, we obtained:
$$s(k(t))=M\cdot\sum_{j=1}^Lc_j(t)\mathcal{FT}\{b_j(r)\rho(r)\}.$$
The solution of the above equation now only requires L FTs.

MRI Experiment
We performed two sets of experiments to evaluate the proposed correction algorithm. In Experiment I, eight healthy subjects (age:46±20, 4 males) were recruited and scanned on a 3T MRI (Prisma, Siemens). Subjects were instructed to stay relaxed, and the B0 changes in the brain during eight-minute time windows were measured using a 3D EPI sequence (resolution:6x6x14mm3, FOV:240x180x144mm3, TE:4.2ms, and volume TR:0.65s). The scans were repeated 6 times for each subject. B0 changes in the head frame were estimated from the co-registered EPI phase data. The obtained data was used to evaluate the validity of our approximation to the EPF. The data was also used to perform simulations where the corruption to a known image was simulated using the measured B0 changes (TE:60ms) and the correction was applied to the corrupted image. In Experiment II, we considered 3D T2*-weighted MRI at 3T (isotropic 2mm resolution, TE:32ms, and FOV:240x180x120mm3). Two (male) subjects were recruited. Subjects were instructed to move their head, and a separate scan served as the reference when subjects stayed still. 3D EPI-based navigators were acquired with spatial resolution of 6x5.6x6mm3 and temporal resolution of 0.5s (for details see Liu et.al4). The T2*-weighted images were reconstructed with different corrections (see Figure 4). The reconstruction performance was evaluated based on the normalized root mean square error (nRMSE) against the reference scan.

Results

The results for an example simulation are presented in Figure 2. We observed that the reconstructions were improved by correcting for the nonlinear B0 fluctuations. The correction improved with more PCA modes and reached a point after which including additional modes did not significantly improve the reconstruction.
We also directly evaluated the validity of our approximate EPF by computing the normalized Frobenius norm of the difference between the full and approximate EPFs. The results for this comparison for all subjects were summarized in Figure 3. The approximation was performed using both PCA and K-means. For a small number of modes/means, K-means slightly out-performed PCA, but as the number of modes/means increased, PCA performed better than K-means.
The results for experiments where subjects were asked to intentionally move, are presented in Figures 4 and 5. We observed that performing a nonlinear correction improved the reconstruction as compared to only a linear correction. The difference between PCA and K-means based reconstructions was not significant from an nRMSE perspective, but we did observe some qualitative improvements in PCA based reconstructions (denoted by arrows). We noted that motion (especially pitch) was greater for subject 1 than 2, we correspondingly observed more artifacts in subject 1. We observed that the overall reconstruction times for PCA and K-means based reconstructions were similar when the number of modes and means was the same.

Discussion and Conclusions

In this work, we showed that PCA can be used to efficiently correct for motion-induced nonlinear B0 changes. PCA-based correction performed similarly to the previously established K-means based approach4 from an nRMSE perspective, with some qualitative improvements observed in PCA-based reconstructions. Systematic evaluation of this approach and other methods, such as the K-means approach, in a larger subject population is warranted in future studies to further establish its efficacy in high field and B0-sensitive applications, such as T2*/susceptibility-weight MRI.

Acknowledgements

The authors gratefully acknowledge funding through the UT Southwestern faculty startup fund. We would also like to thank Yujia Huang for his help with data acquisition.

References

1. Liu, J., de Zwart, J. A., van Gelderen, P., Murphy‐Boesch, J., & Duyn, J. H. (2018). Effect of head motion on MRI B 0 field distribution. Magnetic resonance in medicine, 80(6), 2538-2548.

2. Brackenier, Y., Cordero‐Grande, L., Tomi‐Tricot, R., Wilkinson, T., Bridgen, P., Price, A., ... & Hajnal, J. V. (2022). Data‐driven motion‐corrected brain MRI incorporating pose‐dependent B0 fields. Magnetic Resonance in Medicine.

3. Dong, Z., Wang, F., & Setsompop, K. (2022). Motion‐corrected 3D‐EPTI with efficient 4D navigator acquisition for fast and robust whole‐brain quantitative imaging. Magnetic Resonance in Medicine.

4. Liu, J., van Gelderen, P., de Zwart, J. A., & Duyn, J. H. (2020). Reducing motion sensitivity in 3D high-resolution T2*-weighted MRI by navigator-based motion and nonlinear magnetic field correction. NeuroImage, 206, 116332.

5. Wilm, B. J., Barmet, C., & Pruessmann, K. P. (2012). Fast higher-order MR image reconstruction using singular-vector separation. IEEE transactions on medical imaging, 31(7), 1396-1403.

Figures

Figure 1: Example values of the exponential phase factor (EPF) and its principal modes. The top two rows of images represent the value of the EPF at various time points during a scan. The bottom rows of images represent some of the corresponding principal components.

Figure 2: Results for simulated artifact correction. “No Corr” represents the case when the reconstruction is performed without correcting for the nonlinear variation in the background magnetic field. Difference is between the reconstruction and the reference image. Below each difference image, the overall nRMSE for the reconstruction is presented.

Figure 3: Evaluation of the approximation of the EPF for all subjects in Experiment I. The mismatch between the full EPF and the approximation is evaluated through a normalized Frobenius norm of the difference. Each color represents a subject with the line representing the mean mismatch for the subject, and the error bars representing the full range of mismatches for all scans. In the plot on the left, the approximation was done using PCA, while on the right K-means clustering was used.

Figure 4: Results for Subject 1 from Experiment II. The top images are reconstructions. Ref is the reference. gB0Co includes only global B0 correction. MoCo+LinB0Co also includes motion and linear B0 corrections. MoCo+KM-B0Co and MoCo+PCA-B0Co also correct for nonlinear B0 varaitions using K-means and PCA respectively. The bottom images are the differences in magnitude between each result and Ref as well as a measurement of the subject’s motion. Arrows note regions of qualitative improvement.

Figure 5: Results for Subject 2 from Experiment II. The lay-out of this figure is the same as Figure 4.

Proc. Intl. Soc. Mag. Reson. Med. 31 (2023)
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DOI: https://doi.org/10.58530/2023/4950