Keywords: Motion Correction, Quantitative Susceptibility mapping
Motivation: There is a need for improving UTE-QSM in the human knee joint, which is prone to motion artifacts due to multiple repeated scans required for a short echo spacing.
Goal(s): To investigate the efficacy of motion registration-based UTE-QSM for knee joint imaging.
Approach: We employed rigid affine-based registration and non-rigid deformable registration based on B-spline as a pre-processing step for generating the QSM data.
Results: It is seen that the registration process helps in reducing streaking artifacts and improving UTE-QSM of the knee joint.
Impact: The UTE-QSM technique of the human knee joint is a potentially sensitive biomarker for the diagnosis of musculoskeletal diseases. Motion registration can improve the accuracy of UTE-QSM and hence likely enhance the diagnostic power.
The authors acknowledge grant support from the NIH (R01AR078877, R01AR062581, R01AR068987, R01AR075825, RF1AG075717, K01AR080257 and F32AG082458), Veterans Affairs (I01CX001388, I01CX002211, I01RX002604), and GE Healthcare.
1. Jang H, Sedaghat S, Athertya JS, et al. Feasibility of ultrashort echo time quantitative susceptibility mapping with a 3D cones trajectory in the human brain. Front. Neurosci. 2022;16:1–9 doi: 10.3389/fnins.2022.1033801.
2. Liu S, Wang C, Zhang X, et al. Quantification of liver iron concentration using the apparent susceptibility of hepatic vessels. Quant. Imaging Med. Surg. 2018;8:123–134 doi: 10.21037/qims.2018.03.02.
3. Wei H, Dibb R, Decker K, et al. Investigating magnetic susceptibility of human knee joint at 7 Tesla. Magn. Reson. Med. 2017;78:1933–1943 doi: 10.1002/mrm.26596.
4. Dimov A V., Liu T, Spincemaille P, et al. Joint estimation of chemical shift and quantitative susceptibility mapping (chemical QSM). Magn. Reson. Med. 2015;73:2100–2110 doi: 10.1002/mrm.25328.
5. Jerban S, Lu X, Jang H, et al. Significant correlations between human cortical bone mineral density and quantitative susceptibility mapping (QSM) obtained with 3D Cones ultrashort echo time magnetic resonance imaging (UTE-MRI). Magn. Reson. Imaging 2019;62:104–110 doi: 10.1016/j.mri.2019.06.016.
6. Lu X, Jang H, Ma Y, Jerban S, Chang E, Du J. Ultrashort Echo Time Quantitative Susceptibility Mapping (UTE-QSM) of Highly Concentrated Magnetic Nanoparticles: A Comparison Study about Different Sampling Strategies. Molecules 2019;24:1143 doi: 10.3390/molecules24061143.
7. Jang H, Carl M, Ma Y, et al. Fat suppression for ultrashort echo time imaging using a single-point Dixon method. NMR Biomed. 2019:e4069 doi: 10.1002/nbm.4069.
8. Carl M, Nazaran A, Bydder GM, Du J. Effects of fat saturation on short T2 quantification. Magn. Reson. Imaging 2017;43:6–9 doi: 10.1016/j.mri.2017.06.007.
9. Jang H, Drygalski A, Wong J, et al. Ultrashort echo time quantitative susceptibility mapping (UTE‐QSM) for detection of hemosiderin deposition in hemophilic arthropathy: A feasibility study. Magn. Reson. Med. 2020;84:3246–3255 doi: 10.1002/mrm.28388.
10. Klein S, Staring M, Murphy K, Viergever MA, Pluim JPW. Elastix: A toolbox for intensity-based medical image registration. IEEE Trans. Med. Imaging 2010;29:196–205 doi: 10.1109/TMI.2009.2035616.
11. Reeder SB, Pineda AR, Wen Z, et al. Iterative decomposition of water and fat with echo asymmetry and least-squares estimation (IDEAL): Application with fast spin-echo imaging. Magn. Reson. Med. 2005;54:636–644 doi: 10.1002/mrm.20624.
12. Hernando D, Kellman P, Haldar JP, Liang ZP. Robust water/fat separation in the presence of large field inhomogeneities using a graph cut algorithm. Magn. Reson. Med. 2010;63:79–90 doi: 10.1002/mrm.22177.
13. Liu J, Liu T, De Rochefort L, et al. Morphology enabled dipole inversion for quantitative susceptibility mapping using structural consistency between the magnitude image and the susceptibility map. Neuroimage 2012;59:2560–2568 doi: 10.1016/j.neuroimage.2011.08.082.
14. Liu T, Khalidov I, de Rochefort L, et al. A novel background field removal method for MRI using projection onto dipole fields (PDF). NMR Biomed. 2011;24:1129–1136 doi: 10.1002/nbm.1670.
Figure 1. UTE-QSM. (A) Pulse sequence of 3D dual-echo UTE-cones used for the UTE-QSM data acquisition and (B) schematic of the motion registration-based correction for QSM input data. The dual echo imaging is repeated multiple times at different TEs (TE1 and TE2) by delaying the readout gradient. The raw data is reconstructed as complex images and registered via affine or non-rigid registration techniques before IDEAL and MEDI-QSM process.
Figure 2. The efficiency of motion registration technique (a 32-year-old male volunteer). The echo-subtracted images demonstrate that the unregistered images are susceptible to strong motion, while the registration reduces the motion artifacts, therefore exhibiting less error near tissue boundaries (pointed by yellow arrows).
Figure 3. (A) The phase evolution over six different echoes obtained from a 32-year-old, male volunteer without or with motion registration, and (B) the resultant B0 field maps. The strong error shown in the B0 field map (a red arrow) is presumably due to the strong inter-scan motion that complicates graph cut-based field map estimation in IDEAL.
Figure 4. The feasibility of UTE-QSM for human knee joint via motion registration is presented here. (A) shows maps of 22-year-old, control with mild inter-scan motion. The susceptibility map generated from registered images shows substantial improvement with suppressed streaking artifacts. (B) presents another subject (36-year-old), showing streaking artifacts in the unregistered QSM, which has been corrected through registration. (C) demonstrates another case (23-year-old) with extreme motion creating strong artifacts in QSM, which is mitigated by registration.