Wei-Ching Lo1, John Conklin2,3, Bryan Clifford1, Qiyuan Tian2,3, Daniel Polak2,4, Daniel Nicolas Splitthoff4, Maria Gabriela Figueiro Longo2,3, Azadeh Tabari2,3, Stephen Cauley2,3, and Susie Yi Huang2,3,5
1Siemens Medical Solutions, Boston, MA, United States, 2Department of Radiology, A. A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA, United States, 3Harvard Medical School, Boston, MA, United States, 4Siemens Healthcare GmbH, Erlangen, Germany, 5Harvard-MIT Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA, United States
Synopsis
Scout Accelerated Motion Estimation and Reduction (SAMER) is a novel technique that can mitigate motion artifacts in MR images. In this study, we compared the brain volume and cortical thickness measurements obtained from in vivo motion-free, motion corrupted, and motion corrected images acquired with SAMER to those from a motion-free standard MPRAGE reference scan. The quantitative analysis of motion-free and motion corrected SAMER images showed comparable results with motion-free standard MPRAGE.
Introduction
Volumetric brain MRI is a
powerful tool for the evaluation of patients with neurodegenerative diseases,
providing quantitative biomarkers that can be useful in both clinical and
research settings [1,2]. For example, hippocampal volume inversely correlates
with disease severity in patients with mild cognitive impairment and predicts
the development of Alzheimer disease [3], while cortical thickness measurements
in patients with Parkinson's disease correlate with the clinical stage of
disease and associated dementia [4]. The MRI examination protocol for such
studies typically consists of a 3D T1-weighted MPRAGE acquisition (T1w-MPRAGE) that
provides high spatial resolution and tissue contrast [5], followed by automated
image segmentation and post-processing using software such as FreeSurfer
(http://surfer.nmr.mgh.harvard.edu). However, elderly patients are prone to
motion artifacts, which may degrade the accuracy of volumetric segmentation
[6-8].
Recently, Scout Accelerated
Motion Estimation and Reduction (SAMER) has been proposed and applied to
mitigate motion artifacts in MR sequences, including T1w-MPRAGE [9]. SAMER
combines a fast (3-5 second) scout acquisition with an optimized k-space reordering
to provide data-driven estimates of the rigid body motion parameters for each
k-space shot and provides a robust and computationally efficient framework for
retrospectively reconstructing an artifact free image.
In this
study, we hypothesized that head motion would degrade the accuracy of brain
volume and cortical thickness measurements obtained using FreeSurfer, and that
use of the SAMER approach for motion mitigation could improve the accuracy of
these measurements in the presence of motion. Methods
Three MPRAGE scans were acquired in
vivo at R=4-fold acceleration in an informed and consented healthy
volunteer: (1) motion-free standard reference, (2) motion-free SAMER
acquisition, and (3) motion corrupted SAMER acquisition. All scans were
acquired on a 3T system (MAGNETOM Skyra, Siemens Healthcare, Erlangen, Germany)
using a 20-channel head coil. The sequence parameters used were: FOV 256x256x192mm3;
matrix 256x256x192; TR/TE/TI 2300/3.3/1000ms; flip angles 8°; bandwidth 200 Hz/Px.
The acquisition times were 2:32 min for standard and 2:42 min for the SAMER
acquisitions, respectively. The volunteer was instructed to perform deep breathing
during the motion scan, which is known to introduce motion artifact. The motion
estimation and image reconstruction were performed with an online reconstruction
directly on the scanner and generated additional motion corrected DICOM images.
The FreeSurfer tool [10] was used
for automated human brain segmentation and parcellation of four standard DICOM image
volumes. Regional brain volume and cortical thickness measurements from 11
different brain regions (frontal, parietal, temporal, and occipital lobes; cingulate
gyrus; insula; hippocampus; basal ganglia; brain stem; cerebellum; and cerebral
white matter) were extracted for quantitative analysis. The percentage error in
the volume and cortical thickness measurements was calculated for the SAMER
images with respect to the standard reference scan.Results and Discussion
Figure 1 shows representative
slices from each of the image volumes and indicates that the image quality of motion-free
and motion-corrected SAMER was comparable to the standard reference scan. Significant
motion artifacts present in the motion-corrupted image are substantially
reduced after SAMER motion correction. Figure 1b shows the pial and gray-white
surface outlines from the FreeSurfer segmentation superimposed on the
corresponding images. As can be seen, the segmentation of the motion-free and
motion-corrected SAMER images showed excellent agreement with the reference,
while segmentation of the motion-corrupted scan produced a smaller contour which
potentially excluded some brain tissues.
Substantial reduction in the
estimated brain volume was observed in the frontal, parietal, temporal lobes,
and cerebral white matter of the motion-corrupted scan (Figure 2a). Differences
in cortical thickness (Figure 2b) were found in the temporal and occipital lobe
and insula regions. The highest difference in estimated brain volume (Figure
3a) was in the temporal lobe, where the percentage error for motion-corrupted
images was 28.0%, and 0.3% and 4.3% for motion-free and motion corrected images.
The lowest difference was in the cerebellum, where the percentage error for
motion-corrupted images was 2.4%, and 0.0% and 0.8% for motion-free and motion
corrected images. The motion-corrupted images showed the largest differences of
brain volume in all segmented brain regions and larger differences of cortical
thickness (>11.0%) in temporal lobe, occipital lobe and insula region. The percentage
error of cortical thickness was slightly larger in motion-corrected images as
compared to motion-corrupted images in the parietal lobe and cingulate gyrus,
but the differences in both regions were less than 1.7%. The brain volume and cortical
thickness estimates extracted from motion-corrupted images were biased by head
motion, and the SAMER technique improved the accuracy of brain volume and
cortical thickness measurements in the presence of motion. Our finding matched
to the results reported in [11] that the apparent brain volume loss was
associated with motion. Validation in larger studies including motion prone
clinical populations is warranted.Conclusion
This preliminary study indicates
that brain volumes and cortical thickness estimated using the SAMER motion
correction technique were comparable with those estimated using motion-free standard
MPRAGE. SAMER may be helpful in volumetric studies involving motion prone
patients including elderly patients with neurodegenerative diseases.Acknowledgements
This work was supported in part by NIH research grants: 1P41EB030006-01, 5U01EB025121-03 and Siemens Healthineers.References
1. Rusinek H, de Leon MJ, George
AE, et al. Alzheimer disease: measuring loss of cerebral gray matter with MR
imaging. Radiology. 1991;178(1):109-114. doi:10.1148/radiology.178.1.1984287
2. Lehmann M, Douiri A, Kim LG,
et al. Atrophy patterns in Alzheimer’s disease and semantic dementia: a
comparison of FreeSurfer and manual volumetric measurements. Neuroimage.
2010;49(3):2264-2274. doi:10.1016/j.neuroimage.2009.10.056
3. Frisoni GB, Fox NC, Jack CR,
Scheltens P, Thompson PM, Thompson PM. The clinical use of structural MRI in
Alzheimer disease. Nat Rev Neurol. 2010;6(2):67-77.
doi:10.1038/nrneurol.2009.215
4. Zarei M, Ibarretxe-Bilbao N,
Compta Y, et al. Cortical thinning is associated with disease stages and
dementia in Parkinson’s disease. J Neurol Neurosurg Psychiatry.
2013;84(8):875-882. doi:10.1136/jnnp-2012-304126
5. Mugler JP, Brookeman JR. Rapid
three-dimensional T1-weighted MR imaging with the MP-RAGE sequence. J Magn
Reson Imaging. 1(5):561-567. http://www.ncbi.nlm.nih.gov/pubmed/1790381.
Accessed June 30, 2019.
6. Munn Z, Pearson A, Jordan Z,
Murphy F, Pilkington D, Anderson A. Patient anxiety and satisfaction in a
magnetic resonance imaging department: Initial results from an action research
study. J Med Imaging Radiat Sci. 2015;46(1):23-29. doi:10.1016/j.jmir.2014.07.006
7. Havsteen I, Ohlhues A, Madsen
KH, Nybing JD, Christensen H, Christensen A. Are movement artifacts in magnetic
resonance imaging a real problem?-a narrative review. Front Neurol.
2017;8(MAY):1-8. doi:10.3389/fneur.2017.00232
8. Savalia NK, Agres PF, Chan MY,
Feczko EJ, Kennedy KM, Wig GS. Motion-related artifacts in structural brain
images revealed with independent estimates of in-scanner head motion. Hum Brain
Mapp. 2017;38(1):472-492. doi:10.1002/hbm.23397
9. Polak D, Splitthoff DN,
Clifford B, et al. Scout accelerated motion estimation and reduction (SAMER).
Magn Reson Med. 2021. Epub ahead of print.
10. Fischl B. FreeSurfer.
Neuroimage 2012;62:774–781 doi: 10.1016/j.neuroimage.2012.01.021.
11. Reuter M, Tisdall MD, Qureshi
A, et al. Head motion during MRI acquisition reduces gray matter volume and
thickness estimates. Neuroimage. 2015 Feb 15;107:107-115. doi:
10.1016/j.neuroimage.2014.12.006.