Ross William Mair1,2 and Andre J. van der Kouwe2
1Center for Brain Science, Harvard University, Cambridge, MA, United States, 2Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA, United States
Synopsis
Variations in modern head-coil design lead to
sensitivity differences, changes in intensity profiles, and image SNR. As
morphometric analysis is based on automated analysis of image intensity and
contrast variations, such variation of head coil may be expected to provide
variation in morphometric results. We investigated the morphometric results
from MEMPRAGE scans on subjects scanned in pairs of different head coils. We
saw very limited variation in basic morphometric results from subjects scanned
on the same day in different head coils. Cortical thickness variations are
generally less than 50 µm, although some larger values were observed in
portions of the temporal lobe. Larger differences were observed in volumes of
small sub-cortical structures. These structures often have high variability in
repeat measurements. However, intensity and SNR variations between coils are
often most felt in the deeper regions of the brain, perhaps contributing to
wider variation for these structures.
Introduction
Automated MRI-derived
measurements of human brain volumes from anatomical scans provide novel
insights into normal and abnormal neuroanatomy, but few studies have probed the
effects of sequence-dependent parameters on these measurements.1 The multi-echo
MPRAGE (MEMPRAGE) sequence reduces signal distortion by using a higher
bandwidth and averaging multiple echoes to recover SNR while using variable T2*
decays to enhance contrast, and hence, cortical segmentation.2 To follow
changes longitudinally, or to combine disparate scans into large groups for
disease or impact study, researchers are often faced with the problem of
upgrading technology, in particular improvements in parallel-array head coils
in recent years. Here we investigate the morphometric results from MEMPRAGE
scans on subjects scanned in pairs of different head coils on an older and a
new scanner.Methods
All measurements were
performed using a 3.0 T MRI scanner (Siemens Tim Trio or Siemens Prisma). 11
subjects (mean: 28.0 years, 6 female) were scanned on the Tim Trio in sessions
where the product 12 and 32-channel head coils were used. 10 of 11 subjects
were retested on a different day within a 1-6 week period, so a total of 21
pairs of scans using the 2 head coils were obtained. Retest variation in
individual subjects was not considered here.
7 other subjects (mean: 31.6 years, 4 female) were scanned on a Prisma,
where the product 20, 32 and 64-channel head coils were trialed in one session.
Each session included a MEMPRAGE acquired with recommended Freesurfer
parameters with each head coil (6:03 min, TR/TI = 2530/1200 ms, matrix
256×256×176, resolution = 1 mm iso (no partial fourier), parallel imaging acceleration
= 2, pre-scan normalize enabled). Images were analyzed using FreeSurfer,3 after the pairs of scans from
each subject were aligned using the FreeSurfer robust registration tool.4 An
automated parcellation of the cortex, subcortical and white matter structures
was performed. The 33 cortical regions of the Desikan-Killiany atlas were
combined into five principal cortical lobes for simpler analysis.5 Correlation
and Bland-Altman difference plots were made for the thickness and volume of
each principal cortical lobe determined from each scan, and for the volume of
key sub-cortical structures. Surface-based plots were made to show regions of
thickness difference.Results
Difference-analyses were
performed on all 21 pairs of 12ch and 32ch scans acquired on the same day, and
on all 7 pairs of 32ch and 64ch scans acquired on the same day. The 20ch coil
on the Prisma was not considered at this time. Example Bland-Altman plots for
the Trio and Prisma scans are shown in Fig. 1. The difference analyses for the
cortex are summarized in Fig. 2. For both the Trio and Prisma scans, the cortical
thickness differences for the full lobes are mostly less than 20 µm,
gray-matter volume differences are mostly less than 1%. The sub-cortical volume
measurements show a slightly wider range, up to 4%, due to the small size of
the some of these structures. Bland-Altman slopes were usually within ~ -0.1 –
0.1, indicating no bias with measurement value. Thickness differences from the
Trio scans, plotted on the surface, are shown in Fig. 3.Discussion
Variations in modern
head-coil design lead to sensitivity differences, changes in intensity
profiles, and image SNR. However, coil choice may be made based on the physical
design and how it fits subject’s heads, whether glasses are needed for visual
stimulation/displays during the session, or simply availability. The large
number of options for head coils now means inevitable variation in multi-site
studies, or when data is pooled from existing public sources for new
analysis. As morphometric analysis is
based on automated analysis of image intensity and contrast variations, such
variation of head coil may be expected to provide variation in morphometric
results. The results show very limited variation in basic morphometric results
from subjects scanned on the same day in different head coils. Cortical
thickness variations are generally less than 50 µm, although in the 12ch v 32ch
comparison, larger values are observed in portions of the temporal lobe - however the differences are not significant (Fig. 3b). Its possible the use of
intensity normalization results in increased noise (or lower SNR) in the temporal regions, leading to the small bias in those regions. Where caution is
required is in estimates of volumes of small sub-cortical structures. These structures often have high variability in repeat
measurements, due to their small size and reduced contrast differences.6 However, intensity and SNR variations between coils are often most felt the
deeper regions of the brain, perhaps contributing to wider variation for these
structures.Acknowledgements
Harvard Center for Brain Science; NIH Shared Instrumentation Grant S10OD020039; NIH Grants P41-RR14075,
U24-RR021382References
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