Alberto Di Biase1,2, Alina Schneider3, Rene Botnar1,3,4, and Claudia Prieto1,2,3
1MILLENNIUM INSTITUTE FOR INTELLIGENT HEALTHCARE ENGINEERING, Santiago, Chile, 2School of Engineering, Pontificia Universidad Católica de Chile, Santiago, Chile, 3School of Biomedical Engineering, King’s College London, London, United Kingdom, 4Institute for Biological and Medical Engineering, Pontificia Universidad Católica de Chile, Santiago, Chile
Synopsis
Keywords: Machine Learning/Artificial Intelligence, Machine Learning/Artificial Intelligence, model-based
Motivation: T2 mapping provides quantitative myocardial tissue characterization. However, current approaches acquire several 2D contrast images which are then fitted to a model to estimate the T2 values, leading to limited coverage, and long acquisition and reconstruction times.
Goal(s): Here we propose to speed up 3D whole-heart T2 mapping using a model-based deep learning unrolling network (MEDAL) that leverages the power of machine learning and physical knowledge.
Approach: MEDAL reconstructs the T2 maps directly without reconstructing any intermediate contrast weighted images or fitting.
Results: The proposed approach was evaluated in iNAV-based free-breathing 3D T2 mapping 4x accelerated showing promising results.
Impact: A novel method
for reconstructing parametric maps using a model-based deep learning unrolling network
is presented. The method was demonstrated in a highly accelerated free
breathing 3D whole-heart T2 mapping sequence
allowing for fast and accurate T2 measurements.
Introduction
Parametric maps are an important tool
for diagnosing a number of diseases, including cardiac applications1. Parametric mapping
requires acquisition and reconstruction of different contrast images and is
typically performed in a two-step process. First, the acquired data is
reconstructed to image space using a reconstruction algorithm, such as parallel
imaging or compress sensing. Second, the images are fitted to the signal model (typically
using a mono exponential function or dictionary matching) to estimate the
corresponding relaxometry parameters. The main disadvantage of these approaches
is that they require long reconstruction times, and the acceleration is limited
by the performance of available reconstruction methods.
More recently, model-based
reconstruction approaches have been proposed to estimate the parameters
directly from the acquired k-space data in a single step2. However,
despite promising results, these methods have not gained widespread adoption
because of the difficulty of solving the associated non-linear problem
efficiently. Here we propose to speed up a free-breathing image-navigator (iNAV)-based
3D whole-heart T2 mapping3 using a Model-based rEconstruction by
Deep Algorithm unrolLing (MEDAL) that leverages the power of machine learning
and physical knowledge. The proposed approach was evaluated on healthy subjects.Methods
Model Based Reconstruction
Model based reconstruction is achieved by
solving the following non-linear optimization:
$$\min_\nu || Eq(\nu) - s ||^2_2$$
Where $$$E$$$ is the sampling operator, $$$q$$$ is the signal equation, $$$\nu$$$ the relaxometry parameters (e.g. $$$T_1, T_2, M_0$$$) and $$$s$$$ the acquired k-space data. To stabilize the
solution of this problem, a regularization is typically added4 (e.g.
TV or Wavelets).
Proposed algorithm
MEDAL leverages the power and inference speed of
deep learning with the physical equations of model-based MRI reconstruction
(Fig.1). This is achieved by unrolling a regularized gradient descent algorithm
similar to variational networks5. The algorithm is given by:
$$\nu^{k+1} = \nu^k - \mu^k \frac{\partial Eq(\nu^k)}{\partial \nu}(Eq(\nu) - s) + f_{\theta^k}(\nu^k)$$
This equates to doing gradient descent
with step size $$$\mu^k$$$ on a regularized version of the problem were the network outputs the gradient of the regularizer. The
network architecture is a U-net and a different set of weights is used for each
iteration.
The step size $$$\mu^k$$$ is also learned. A single network with multiple channels is used to regularize all
parametric maps simultaneously. Here 5
iterations are used for finding the final solution. MEDAL differs from the method proposed by ref6 in two ways: 1) zero-fill images are
used to find the starting maps for optimization while ref6 use a
separate network and 2) for regularization ref6 use a different
network for each map whereas MEDAL uses a single network for all maps.
Coil sensitivities were estimated using ESPIRiT7. The output from
the last module are the predicted maps and are compared with the gold standard
map using the SSIM loss. As an additional term, we penalize the
SSIM difference between the images generated using the predicted maps and the signal
model, and the gold standard
reconstruction.
Experiments and Results
The proposed approach was applied to
speed up free-breathing iNAV-based 3D whole-heart T2 mapping. The sequence3
(Fig.2) includes three T2 preparation pulses (T2prep 0,
28, 55ms), a 3D Cartesian variable density with spiral profile order8 with 4x undersampling and iNAVs to
correct for beat-to-beat translational motion. To obtaining a gold standard
reconstruction, images were reconstructed using HD-PROST9 and an
exponential fitting was performed to find $$$T_2$$$ and $$$M_0$$$. The DFT
on the read-out direction is performed, and the network is trained on 2D
slices. The k-space was zero padded to bring all images to the same matrix size
and a Hamming window was applied to reduce ringing artifacts. The proposed
approach was trained and evaluated on 23 acquisitions on healthy subjects and
patients. Sixteen volumes were used for training, 4 for validation and 3 for
testing. To normalize the inputs, the k-space is divided by the maximum of the
zero fill for the first T2prep image.
Results from 2 subjects (testing set) are shown in Fig. 3 for the proposed MEDAL method in
comparison to gold standard HD-PROST. Similar visual map quality is observed
between both methods. T2 bullseye plots reconstructed with the proposed
method (MEDAL) and the gold standard are shown in Figure 4. Inference reconstruction
times were 8s and 5min for MEDAL and HD-PROST.Conclusions
A novel method for reconstructing
parametric 3D whole-heart T2 maps using a model-based deep learning unrolling
network is presented. The method enables acquisition in 6min with a fast
reconstruction of 8s, achieving similar map quality than the gold standard.
Evaluation in a larger cohort of subjects and extension to no-rigid motion
correction will be investigated as future work. Acknowledgements
The authors acknowledge financial support
from: (1) BHF RG/20/1/34802 (2) EPSRC EP/V044087/1 (3) ANID Millennium
Institute iHEALTH, ICN2021_004; Fondecyt 1210637 and 1210638References
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