Gastao Cruz1, Thomas Kuestner1, Ilkay Oksuz1, Olivier Jaubert1, Niccolo Fuin1, Andy P. King1, Julia A. Schnabel1, René M. Botnar1, and Claudia Prieto1
1Biomedical Engineering Department, School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom
Synopsis
Conventional Magnetic Resonance Fingerprinting (MRF)
relies on pixelwise dictionary matching of highly undersampled time-series
images. However, remaining aliasing artefacts in these images can compromise the
matching step and thus affect the accuracy of the parametric maps. Dictionary-based
compression has been proposed to exploit redundancies in the signal evolution
dimension, however these approaches do not exploit tissue redundancies within
the images. Here we propose to leverage redundant information between similar
tissues and the MRF dictionary to suppress residual artefacts along time, using
long short-term memory (LSTM) networks. Preliminary results indicate that proposed
MRF-LSTMs can suppress aliasing in highly undersampled scenarios.
INTRODUCTION:
Magnetic Resonance Fingerprinting (MRF1)
samples the magnetization transient state via highly undersampled images to
produce multi-parametric maps (e.g. T1, T2, T2*). Despite some resistance to
incoherent artefacts, aliasing can propagate from the undersampled images to
the resulting maps2,3. Iterative reconstruction approaches have been
proposed to estimate images free of artefacts. In particular, locally low rank
(LLR)4,5 and dictionary-based regularization3 have been proposed
to exploit redundancies in the MRF signal evolution and have shown to suppress
residual noise-like artefacts. Fully connected networks and recurrent neural network that exploit the
time-dependent information of the MRF signal evolution (fingerprint) have been
proposed to learn the maps without direct dictionary matching6,7.
Spatial-temporal convolutional neural networks have been proposed to take advantage of the information between neighbouring
fingerprints8. However, these approaches may not necessarily exploit non-local tissue
redundant information within the field of view. Here we train a neural network of long
short-term memory (LSTM)9 units, leveraging both similar tissue-temporal
signal evolutions and MRF dictionary prior information to reduce artefacts in
resulting MRF maps. The proposed network was evaluated in realistic brain simulations
and compared against low-rank inversion (LRI) reconstruction and LLR denoising.METHODS:
The proposed framework for MRF denoising is
outlined in Fig.1, which acts in dictionary-based temporally compressed
singular images3 (resulting from an LRI reconstruction) of size [Ny, Nx, Nr],
where Ny and Nx are the image spatial dimensions and Nr
is the number of singular images. Data is processed for each pixel separately,
according to the following steps. 1) For each pixel in the singular images, a
non-local neighbourhood of Nt self-similar tissues is obtained via
exhaustive inner product with every other voxel (Fig.1a). 2) Each neighbourhood
(containing multiple pixels over several singular images) forming the input
signal of the MRF-LSTM network is stored in the first dimension (blue signal)
of a NtNrx2 singular-neighbourhood matrix representing
the singular pixels for this tissue neighbourhood. The corresponding signal matches
(green signal) with the MRF dictionary are obtained (also via inner-product) and
stored in the second dimension (Fig1.b). 3) This information is fed into the
proposed MRF-LSTM network consisting of LSTMs with 3 layers: 200 LSTM units,
100 LSTM units and 1 LSTM unit, producing a denoised tissue group (Fig.1c). This
procedure is independently performed for every pixel in the image and finally
results are re-aggregated into the shape of the singular images.EXPERIMENTS:
Brain T1, T2 and M0 maps obtained in previous
in-vivo experiments in five healthy subjects were used as ground-truths for the
simulation experiments. An acquisition was simulated based on pseudo-steady
state MRF10 with the following key parameters: initial inversion
recovery pulse, balanced steady state readout, TE/TR = 2/4.4 ms, 1x1 mm2
resolution, varying flip angle according to10 and golden radial
trajectory with one readout per time-point. The tissue neighbourhood Nt
was 200 and the LRI rank Nr was 8. The simulation was performed with varying signal-to-noise
ratio (SNR) levels ([20, 10, 5]) and varying number of time-points ([1000,
2000]). Singular images were reconstructed from this simulated data via LRI,
which still contained residual streaking and blurring artefacts from
radial undersampling. LRI reconstructed singular images formed the input for both
the MRF-LSTM denoising and LLR denoising. The proposed MRF-LSTM framework was
applied to the magnitude of reconstructed singular images and compared with LLR
reconstruction (which used the complex signal). Ground-truth singular images (labels) were generated via the
same simulation framework, based on fully sampled images. The MRF-LSTM network
was trained with data from four healthy subjects resulting in approximately 1
million singular-neighbourhood training samples, 30 epochs, 0.01 learning rate,
ADAM11 optimizer, mean square error loss, 10% validation data. A
fifth healthy subject dataset was used for testing. Resulting T1/T2 maps were
obtained via inner-product with the MRF dictionary in all cases.RESULTS:
The proposed MRF-LSTM network was able to
suppress undersampling artefacts in the singular value images to a higher
degree than LLR, which is more visible in singular images with higher rank
(Fig.2). When inspecting the resulting parametric maps the MRF-LSTM also
achieved higher aliasing suppression than LLR and LRI (Fig.3). However, in
these preliminary results the MRF-LSTM network failed to distinguish between
white and grey matter, introducing a negative bias for grey matter in the
parametric maps, possibly due large tissue
grouping or excessive artefacts in the training samples. This bias can be seen
in the T1 and T2 values obtained in regions of interest for white matter and grey
matter in Table 1.CONCLUSION:
An
MRF-LSTM network was proposed for denoising of highly-undersampled MRF images,
combining information from similar tissues and MRF dictionary prior information.
Preliminary results suggest this approach could act as a powerful denoiser,
however further network training is needed to better distinguish between white and grey
matter in the parametric maps. Future work will improve the existing network
and incorporate an improved network into a model based deep learning
reconstruction to enforce data consistency within a LRI-based reconstruction.Acknowledgements
ACKNOWLEGDMENTS:
This work was
supported by EPSRC (EP/P001009, EP/P032311/1) and Wellcome EPSRC Centre for
Medical Engineering (NS/ A000049/1).References
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