Poster No:
1921
Submission Type:
Abstract Submission
Authors:
Omer Faruk Gulban1,2, Andreas Deistung3, Desmond Ho Yan Tse4, Saskia Bollmann5, Renzo Huber6, Rainer Goebel1,2, Kendrick Kay7, Dimo Ivanov1
Institutions:
1Maastricht University, Maastricht, Netherlands, 2Brain Innovation, Maastricht, Netherlands, 3Polyclinic for Radiology, University Hospital Halle, Halle, Germany, 4Scannexus, Maastricht, Netherlands, 5School of Electrical Engineering and Computer Science, The University of Queensland, Brisbane, Queensland, 6National Institutes of Health, Washington, MD, 7Center for Magnetic Resonance Research, Department of Radiology, University of Minnesota, Minneapolis, MN
First Author:
Omer Faruk Gulban
Maastricht University|Brain Innovation
Maastricht, Netherlands|Maastricht, Netherlands
Co-Author(s):
Andreas Deistung
Polyclinic for Radiology, University Hospital Halle
Halle, Germany
Saskia Bollmann
School of Electrical Engineering and Computer Science, The University of Queensland
Brisbane, Queensland
Renzo Huber
National Institutes of Health
Washington, MD
Rainer Goebel
Maastricht University|Brain Innovation
Maastricht, Netherlands|Maastricht, Netherlands
Kendrick Kay
Center for Magnetic Resonance Research, Department of Radiology, University of Minnesota
Minneapolis, MN
Dimo Ivanov
Maastricht University
Maastricht, Netherlands
Introduction:
Unlike magnitude images, even simple averaging is difficult with phase images, because of the circular nature of phase, spanning 2pi radians range. There is a well-developed literature on how to process phase images [1-5]. However, there are also well-known challenges that arise, such as still remaining phase wraps in regions with low signal-to-noise ratio (SNR) after phase unwrapping or removal of background fields. While employing these methods help make phase images more accessible for end users, using phase data is less practical and less commonplace compared to magnitude images. In our own research that uses mesoscopic imaging (<0.5 mm iso.) at 7 T, we need to average multiple acquisitions to increase image signal-to-noise ratio (SNR). To address this problem, we propose to operate on the magnitude of the 2nd spatial derivative of phase images - coining the term "phase jolt".
Methods:
We compute spatial partial derivatives of the phase images through the "circular differences". This operation accounts for the "phase wraps" at pairwise computations. For each voxel in a 3D MR phase image, we compute the circular differences along x, y, z axes to obtain the first spatial phase derivative image. The 1st spatial derivative is a "vector field", where each voxel has three values associated with it (as opposed to the initial scalar phase field, where each voxel has a single value associated with it). Note that the circular differences are always in -pi to pi radians range, where the sign indicates clockwise or counterclockwise direction. Once the 1st spatial derivative is computed, we quantify the magnitude of the vectors using the L1 norm divided by 3. We call this spatial operation "phase jump".
The phase jump images highlight tissue edges; however, they also reveal the large-scale phase variations originating from the background field (Fig 1). To account for this, we suggest the 2nd spatial derivative of the phase images. We compute this by taking the spatial derivative of the 1st spatial derivative vector field, resulting in a "tensor field" (where each voxel has 9 values associated). Then, we compute the magnitude of the 2nd spatial derivative using the L1 norm divided by 9. This magnitude calculation again results in a natural 0 to pi radians range. We call this spatial operation "phase jolt". The benefits of computing the phase jolt are the same as for the phase jump while further mitigating the bias field (Figure1). The downside is that it requires integrating even more information than the phase jump, therefore lowering the effective resolution.
We compute the phase jump and jolt on the data acquired as described by [6] using a multi echo gradient echo protocol [7] at 7 T with pTx [8]. Briefly, we have 6 echoes at 0.35 mm isot. resolution, using low acceleration.
Results:
Fig 1A shows the phase jump and jolt contrasts compared to the corresponding T2*-weighted magnitude and phase images. Fig 1B highlights that phase images are hard to average due to their circular nature. However, phase jolt images are easy to average due to their numerical range with natural zero and maximum (pi radians).
Fig 2 demonstrates the benefit of phase jolt over phase jump, especially for mitigating the background field.

·Figure 1.

·Figure 2.
Conclusions:
Phase jolt contrast is easy to compute and implement (several voxel-wise circular subtractions, and L1 norm). It provides an informative image where vessels are enhanced while the background field is mitigated. Therefore, phase jolt images may provide an additional contrast in any setting where phase images are recorded. The exquisite contrast of venous vessels in the phase jolt image might be used in a similar setting as susceptibility weighted imaging (SWI) where it may serve to create a phase mask to enhance the sensitivity towards vessels in T2*-weighted images. Additionally, phase jolt images can also be computed on fMRI data. Our implementation is available within the LayNii software package [10] via LN2_PHASE_JOLT program.
Modeling and Analysis Methods:
Methods Development 1
Novel Imaging Acquisition Methods:
Anatomical MRI 2
Keywords:
ANGIOGRAPHY
Cortical Layers
HIGH FIELD MR
MR ANGIOGRAPHY
MRI
MRI PHYSICS
STRUCTURAL MRI
Structures
Sub-Cortical
Other - Mesoscopic
1|2Indicates the priority used for review
Provide references using author date format
[1] Deistung, A., Rauscher, A., Sedlacik, J., Stadler, J., Witoszynskyj, S., Reichenbach, J.R., 2008. Susceptibility weighted imaging at ultra high magnetic field strengths: Theoretical considerations and experimental results. Magnetic Resonance in Medicine 60, 1155–1168. https://doi.org/10.1002/mrm.21754
[2] Haacke, E.M., Mittal, S., Wu, Z., Neelavalli, J., Cheng, Y.-C.N., 2009. Susceptibility-Weighted Imaging: Technical Aspects and Clinical Applications, Part 1. AJNR Am J Neuroradiol 30, 19–30. https://doi.org/10.3174/ajnr.A1400
[3] Deistung, A., Schweser, F., Reichenbach, J.R., 2017. Overview of quantitative susceptibility mapping. NMR in Biomedicine 30, e3569. https://doi.org/10.1002/nbm.3569
[4] Robinson, S.D., Bredies, K., Khabipova, D., Dymerska, B., Marques, J.P., Schweser, F., 2017. An illustrated comparison of processing methods for MR phase imaging and QSM: combining array coil signals and phase unwrapping. NMR in biomedicine 30. https://doi.org/10.1002/nbm.3601
[5] Dymerska, B., Eckstein, K., Bachrata, B., Siow, B., Trattnig, S., Shmueli, K., Robinson, S.D., 2021. Phase unwrapping with a rapid opensource minimum spanning tree algorithm (ROMEO). Magnetic Resonance in Med 85, 2294–2308. https://doi.org/10.1002/mrm.28563
[6] Gulban, O.F., Bollmann, S., Huber, L. (Renzo), Wagstyl, K., Goebel, R., Poser, B.A., Kay, K., Ivanov, D., 2022. Mesoscopic in vivo human T2* dataset acquired using quantitative MRI at 7 Tesla. NeuroImage 264, 119733. https://doi.org/10.1016/j.neuroimage.2022.119733
[7] Eckstein, K., Dymerska, B., Bachrata, B., Bogner, W., Poljanc, K., Trattnig, S., Robinson, S.D., 2018. Computationally Efficient Combination of Multi-channel Phase Data From Multi-echo Acquisitions (ASPIRE). Magnetic resonance in medicine 79, 2996–3006. https://doi.org/10.1002/mrm.26963
[8] Tse, D.H.Y., Wiggins, C.J., Ivanov, D., Brenner, D., Hoffmann, J., Mirkes, C., Shajan, G., Scheffler, K., Uludağ, K., Poser, B.A., 2016. Volumetric imaging with homogenised excitation and static field at 9.4 T. Magnetic Resonance Materials in Physics, Biology and Medicine 29, 333–345. https://doi.org/10.1007/s10334-016-0543-6
[9] Huber, L., Poser, B.A., Bandettini, P.A., Arora, K., Wagstyl, K., Cho, S., Goense, J., Nothnagel, N., Morgan, A.T., van den Hurk, J., Müller, A.K., Reynolds, R.C., Glen, D.R., Goebel, R., Gulban, O.F., 2021. LayNii: A software suite for layer-fMRI. NeuroImage 237, 118091. https://doi.org/10.1016/j.neuroimage.2021.118091