Ruogu Matthew Zhu1, Nicole Seiberlich2, and Yun Jiang2
1Department of Electrical and Computer Engineering, University of Michigan, Ann Arbor, MI, United States, 2Department of Radiology, University of Michigan, Ann Arbor, MI, United States
Synopsis
Low
SNR is a challenge for magnetic resonance fingerprinting (MRF) at low-field
(0.55 T). In this work, we apply a locally low rank denoising method based on
elimination of noise-only principal components according to the
Marchenko-Pastur distribution to MRF data. We show that this method is
effective at denoising both phantom and in vivo MRF images.
Introduction
The goal of this study is to improve the accuracy and precision
of T1 and T2 estimations from MR Fingerprinting (MRF) by reducing thermal noise
at 0.55 T. A recently introduced 0.55T system has shown potential for efficient
imaging due to shorter T1 and longer T2/T2* values with a reduced cost compared
to higher field scanners, such as 1.5T or 3T1. While MRF2 has been shown to be an
efficient and accurate method for quantifying relaxation times, the low
signal-to-noise ratio (SNR) at 0.55T may reduce the accuracy and precision of
T1 and T2, and restrict the achievable spatial resolution, reducing the
potential clinical utility of this approach.
Here we propose a denoising algorithm3 that matches the acquired
signal to a general noise model4, and then removes the noise
components before dictionary matching to improve the precision of
MRF estimations at 0.55T.Methods
The denoising algorithm uses a local low-rank process to
decompose 3x3 voxel patches of MRF time-series data into their principal
components using singular value decomposition (SVD). The generated singular
values are matched to the Marcheko-Pastur (MP) distribution, a general noise
model describing the singular value spectrum of random matrices. Once the noise
components are identified, they are removed, and the data matrix is
reconstituted without them.
Data were collected using a 2D FISP MRF sequence5 with variable flip angles ranging
from 5° to 75°, a 1x1 mm in plane spatial resolution, a fixed TR of 18 ms, and
a TE of 5.6 ms on a 0.55T scanner
(MAGNETOM Siemens Free.Max Siemens Healthcare, Erlangen, Germany). 2500 time
points were acquired with an acquisition time of 45 seconds for a 2D slice. Noise
pre-whitening6,7 was applied to the MRF data
to remove spurious correlations between phase array coils. T1 and T2 maps were
generated from the MRF data both before and after thermal noise removal via
pattern matching using a dictionary with 10-5000 ms T1 entries and
2-1200 ms T2 entries with entry step size between 2-500 ms.
The T2 layer of an ISMRM/NIST MR system phantom was scanned
to assess noise removal properties. A slice
thickness of 1.5 mm was used. Relaxation times from MRF were compared with
reference values measured by gold standard spin-echo methods. T2 measurements
with reference values greater than 500 ms were excluded since they do not
correspond to physiological values.
In vivo brain and liver data were acquired in health
subjects in an IRB approved study. Brain image data was acquired with both a 5
mm and 1.5 mm slice thickness; the thinner slice was collected to assess
denoising performance at extremely low SNR. Liver images were acquired with an 8
mm slice thickness.
Noise was quantified through both SNR and standard
deviation, where SNR is defined as the mean divided by the standard deviation
for either a single voxel across multiple scans or for a uniform group of
voxels. The noise reduction was determined by
comparing the SNR and standard deviation of parameter maps.
σ-normalized residuals are calculated by the difference
between a parameter map and a reference sample mean from repeated measurements
divided by the standard deviation of the repeated measurements. Residual maps
can be thought of as error from an approximate true image. Accurate
parameter maps should have a small difference with the reference and lack
anatomical detail.Results
Figure 1 shows images and measured relaxation times for each
sphere from the phantom data. The standard deviation, shown in the error bars,
is reduced with denoising for all spheres.
Figure 2 shows denoising performance on a 1x1x5 mm
resolution scan of a brain. ROIs are drawn for white matter, gray matter, and cerebrospinal
fluid. Relaxation time measurements have a good agreement with results reported
in literature8. Standard deviations are
reduced by as much as a factor of 1/3rd which translates to an SNR improvement
by approximately a factor of 2-3 after applying denoising. Mean measurements in
each ROI typically experienced a 2% change, with only one ROI experiencing a 7%
change.
Figure 3 shows denoising performance on liver data.
Relaxation time measurements within an ROI show that standard deviation is more
than halved with denoising. The mean relaxation times experience less than 1 ms
change with denoising.
Figure 4 shows the 10-mean σ-normalized residual of denoised
brain images at 1.5 mm slice thickness calculated from a 10-average reference
image. The residuals contain small amounts of anatomical detail: only
cerebrospinal fluid and the skull.
Discussions and Conclusions
The denoising method was shown to be effective at denoising
MRF data collected at 0.55T, resulting in improved SNR and measurement
precision. Denoising does not result in an improvement in measurement accuracy
as the actual relaxation measurements experienced only small changes. Residuals
show that denoising does not introduce much bias into the image since the
residuals largely lack anatomical detail. The cerebrospinal fluid that can be
seen is likely due to physiological fluctuation in the relaxation times. In the
skull region, the residual shows smaller mean error, which indicates that
denoising produces more precise measurements in the skull. This denoising
method could be useful for improving low-field MRF and enhance the diagnostic
utility of low-field MR systems.Acknowledgements
This
work was supported by Siemens Healthcare and NIH grants R37CA263583 and
R01CA208236.References
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