Wanyong Shin1 and Mark J Lowe1
1Radiology, Cleveland Clinic, Cleveland, OH, United States
Synopsis
Keywords: Motion Correction, Brain, Head motion, fMRI
We investigate the source of residual motion artifact after volumetric motion correction using a custom MR sequence acquisition with prospectively injected motion (SIMPACE). We injected various patterns of motion during scanning ex-vivo brain phantoms at 3T to synthesize head motion in an fMRI dataset. We propose voxelwise retrospective motion regressors in addition to 6 rigid body motion parameters, then compare it with the “standard” 6 motion parameters and their derivatives regressor models. The proposed model improves tSNR by 40% and 11% in linear drift of motion and the realistic motion case, respectively, compared to 6 motion parameter model.
Introduction
Head motion is largely considered to be the most dominant non-neuronal source, present in human fMRI data 1, 2. Since the residual motion artifact remains even after perfect volume motion 3, various methods have been proposed to utilize “retrospective motion regressors” which are regressed out after motion correction to attempt to ameliorate these residual effects of head motion 4-7. In this study, we investigate the source of the residual motion artifact using data from a custom MRI acquisition with prospectively injected motion and propose voxelwise motion regressor in addition to 6 rigid body motion parameters.Methods
Ex-vivo brain
We built ex-vivo whole brain phantom 8, and scanned at 3T (see Fig1A-F).
MR acquisition
We modified Prospective Acquisition CorrEcted (PACE) EPI sequence 9 to inject the motion, referred as Simulated PACE (SIMPACE) sequence 5. Note that SIMPACE sequence alters the direction and amplitude of the gradient axes during the scanning, synthesizing inter-/intra-volume motion effect on the collected images. In this study, we only test inter-volume motion.
Using SIMPACE sequence (voxel size=2x2x4mm3, TR/TE=2s/28ms, 21 slices), we synthesized 3 different head motion patterns; A) impulse shift (4mm) in z-direction and rotation (4°) motion along x-/y-axes during 2s. B) linearly increasing shift and rotation (up to 4 mm/°) in x-/y-/z-direction during 60s. C) 10 realistic head motion cases, measured from 10 rs-fMRI HCP YA data using 3dvolreg, AFNI 10. Six rigid body motion parameters with 1/0.8s of sampling rate is interpolated to 2s of TR in SIMPACE.
Partial volume (PV) regressor
Fig2.A-D shows the example of SIMPACE B dataset. Y-directional drift of shift motion is injected up to 4mm, corresponding to 2 voxel shift, shown in Fig2.B. The time-series at a green voxel is plotted before (Fig2.C) and after (Fig2.D) motion correction. Note that the residual signal (Fig2.D) is bounded two times to 2mm of voxel dimension, which does not agree with the previous findings 3-7.
Volume motion is injected negatively on each static image to simulate the motion corrupted data, presented by Wilke 11. This simulated motion data is identical to “MotSim” in the previous work 12. Motsim is volume motion corrected to the reference, synthesizing the residual artifact. We use this output as voxelwise PV regressor. The workflow is displayed in Fig2.E-H.
Data analysis
All motion corrected SIMPACE data in this study is generated with known injected motion.
Dataset A: Student t-score maps are calculated on volume motion corrected SIMPACE data to the motion parameter (MoPa) and their derivative (Deriv). In addition, temporal ICA analysis is conducted 13.
Datasets B and C: Temporal signal-to-noise ratio (tSNR) is calculated after volume motion correction and regress-out of 1) PV, 2) MoPa, 3) MoPa+PV and 4) MoPa+Deriv. Note that degree-of-freedom (DOF) of MoPa is 1 and 6 in B) and C) datasets, respectively. Averaged tSNR is reported in grey matter mask.Results
Figure1.G shows the example of SIMPACE data with drift of z-axis rotational motion. Fig1.H plots the signal at the same voxel but generated by image post-processing. SIMPACE data is different with simply re-sampled data, as shown in blue arrows.
The spin history effect is minimal with SIMPACE data of TR=2s. Impulse z-directional voxel shift alters the time interval of each slice acquisition with ± half of TR at 6th and 7th volumes, shown Fig3.B. ICA analysis does not detect the spin history effects either, as shown in Fig3.C and D.
The proposed PV regressor predicts the residual motion better than MoPa, resulting in tSNR with PV (147±26) and with MoPa (118±27) in the case of 6 linear drift motion cases, as shown in Fig4.A. The maximum tSNR is observed with 166±25 when MoPa+PV model is used. MoPa regressor model outperforms PV regressor in the case of realistic motion, resulting in 199±30 (MoPa) and 170±31 (PV) of tSNR. The maximum tSNR (222±18) is observed when MoPa+PV model is employed.
Figure 5 shows where PV regressor is highly correlated to rigid volume motion in the realistic motion case.Discussion
While 6 rigid motion parameters have been used as effective motion regressor in fMRI analysis3 6, additional voxelwise displacement or its derivatives were proposed to remove the residual motion artifact 4, 5. Bullmore’s regressor model has 24 regressors and Beall’s model has 14. This study proposes single voxelwise regressor in addition to 6 rigid motion parameters. With the loss of single DOF, the proposed MoPa+PV model improves tSNR on average by 40% in the case of linear drift motion and 11% in the more realistic head motion cases.
While PV regressor predicts the residual artifact after linear drift motion correction better than MoPa, MoPa regressors outperforms PV in realistic head motion SIMPACE data. It could be explained that the realistic head motion is continuous and random 7 and 6 DOF rigid motion parameter model more effectively removes the large variances than the single PV.
It should be noted that the standard deviation of tSNR with Mopa+PV model across 10 subjects is the smallest of 18, compared to other models (31, 30 and 30 in PV, MoPa and MoPa+deriv models), indicating that MoPa+PV model suppress the individual variation of residual motion even after the different pattern of head motions. Acknowledgements
Authors acknowledge technical support by Siemens Medical Solutions.
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