Nahla M H Elsaid1, Nadine L Dispenza2, R Todd Constable1,3, Hemant D Tagare1,2, and Gigi Galiana1
1Radiology and Biomedical Imaging, Yale School of Medicine, New Haven, CT, United States, 2Department of Biomedical Engineering, Yale University, New Haven, CT, United States, 3Neurosurgery, Yale University, New Haven, CT, United States
Synopsis
This work presents quantitative T2-maps
and a full T2w-image series generated from an ordinary single contrast T2w-dataset
using the growing Constrained Alternating Minimization for Parameter mapping (g-CAMP)
reconstruction method. Simulated data were used to study the accuracy of this
approach under various echo spacings and with added noise, and the method is also demonstrated
in an experimental T2w-dataset. This
could ultimately lead to retrospective parameter mapping using data from
standard single-contrast acquisitions.
Introduction
Quantitative T2-maps have many advantages over
grayscale T2w-images as they show greater consistency across multi-site studies
and for machine learning applications 1, but
their long acquisition time makes them difficult to perform routinely. While many groups have shown that faster T2-mapping
can be accomplished by appropriate regularization across the echo series, prior
work has focused on evenly spaced sampling at each echo. 2 However,
a standard T2w-scan can be regarded as a kind of undersampled T2-mapping
sequence with block-like k-space sampling at each echo. Because CAMP 3 (Constrained Alternating Minimization
for Parameter mapping) is a very general reconstruction scheme compatible with any
acquisition pattern across the echoes, the CAMP extension to g-CAMP (growing CAMP)
was found to generate quantitative T2-maps from data traditionally acquired for
a single grayscale T2w-image. CAMP alternates between optimizing the image
series and the parameter map, but it does so by minimizing a single cost-function that incorporates both (1) consistency between each individual
parameter image and its k-space data and (2) adherence of the image series to
the relaxometry model for each pixel. In g-CAMP, the standard CAMP method 3
is applied first to the center two bands of k-space, then
it grows in each direction until it includes all the bands of k-space from the whole T2w-dataset.Methods
CAMP
In MR parameter mapping, the complete MRI signal
vector
$$$S(k)$$$ is regarded as a series of signal vectors $$$S_p (k)$$$, each of which samples the k-space $$$k$$$ of a complex weighted image $$$m_p$$$ acquired at different
parameter encoding values (e.g., echo
time TE), through the encoding
matrix $$$E_p$$$ for a total of $$$p$$$ images, where $$$p$$$
is also the number of
echo times sampled.
As described in 3, the relationship of
each parameter map relative to the previous one is $$$m_{(p+1)} (x)=m_p (x)α(x),$$$ where $$$α(x)=exp(\frac{-p∆TE}{T_2 (x)})$$$. Incorporating this, the
CAMP objective function is $$$J=J_1+J_2+J_3$$$, where
$$$J_1=∑_{(p=1)}^P‖S_p-E_p m_p ‖^2$$$ is the
data fidelity term, $$$J_2=τ∑_{(p=1)}^PTV(m_p )$$$ is a TV-norm
regularization term,
and finally, $$$ J_3=λ∑_{(x=1)}^N∑_{(p=1)}^{(P-1)}‖m_{(p+1)} (x)-α(x)
m_p (x)‖^2 $$$ is the
CAMP constraint. $$$τ$$$ and $$$λ$$$ are
both weighting parameters. The CAMP objective function $$$J$$$ is
alternately minimized with respect to $$$m_p$$$ (fixed $$$α$$$) using a
non-linear conjugate-gradient method (Polak-Ribiere). 4 It is then minimized with respect to $$$α$$$ (fixed $$$m_p$$$), keeping in mind that $$$α$$$ is real. This loop is repeated
until both $$$m_p$$$ and $$$α$$$ converge.
g-CAMP
As shown in Figure 1,
the g-CAMP algorithm starts by using only the two center bands of k-space. A
CAMP reconstruction on these two bands continues for several iterations until
it converges. Except for the middle two images, each image is initialized before
entering the CAMP loop as a uniformly scaled version of the previously
reconstructed neighboring image, using a scale factor derived from the middle
bands of data. In addition, the phase of
each
$$$m_p$$$ is assumed to be that of the standard grayscale
T2w-image. This is implemented by
incorporating that phase into $$$E_p$$$ and forcing each
update to the $$$m_p$$$ series to be real.
Simulation
Data were simulated to mimic a single T2w-acquisition,
where k-space is acquired blockwise across 8 echoes, and the center of k-space
was acquired at the 4th echo.
Digital-phantoms for each echo time were generated using a T2-template
and a proton-density (PD) template, and appropriate gradient and coil encodings
were applied to each phantom to generate the multi-echo data. Coil weightings were derived from
experimental coil profiles in an eight-channel coil. Random Gaussian noise with zero mean and a standard deviation of 2% of the ℓ2-norm
of the signal was added to the data.
Imaging
T2w-images were acquired on a 3T MRI
scanner (MAGNETOM Trio Tim, Siemens Healthcare, Erlangen, Germany). A Cartesian
TSE sequence was used with TR=2500 ms, ETL= 8 and
TE=21 ms,
with a base-resolution of 128, 3mm slice thickness.Results
The Cartesian simulation results in
Figure 2 demonstrate g-CAMP applied to different echo spacings, where the difference
images between ground truth and g-CAMP reconstructions show median absolute deviation (MAD) errors between
2.2 to 3.2 ms and root-mean-square-error (RMSE) between 5.6 to 7.6 ms. A scatter plot of ground truth vs.
reconstructed T2 values produces an adjusted R2 of
0.9606-0.9865. A zoomed-in box of the ΔTE=20 ms T2-map (Figure
3) shows that the resolution is not compromised by g-CAMP. Figure
4 shows the full image series generated from each reconstruction which, like
the T2-maps, is in good agreement with the ground truth. Having done extensive simulations, we are now
in the process of applying g-CAMP to experimental data. Even the application of the previous simpler
algorithm (CAMP) to existing T2w data shows promise (Figure 5), with contrast
and numerical values consistent with the literature.Discussion and Conclusion
This work demonstrates
the potential of g-CAMP to retrospectively reconstruct quantitative T2-maps
from data acquired for a standard single-contrast T2w-acquisition. While this work applies g-CAMP to quantitative
T2-mapping, g-CAMP can also be extended to T1 relaxation by adding an intercept
to the relaxation model. Therefore,
there may be potential to retrospectively process TSE and MPRAGE imaging data to
calculate accurate T2 and T1-maps respectively.Acknowledgements
We note that both Dr. Galiana and Dr.
Tagare contributed equally as senior authors on this work. This work was
funded by the National Institutes of Health under R01EB022030, R01EB012289,
4R01 EB016978, and K01EB16897.References
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