Dhritiman Das1,2, Eduardo Coello1,2, Axel Haase1, Rolf F. Schulte2, and Bjoern H. Menze1
1Technical University of Munich, Garching, Germany, 2GE Global Research, Munich, Germany
Synopsis
We
present a data-driven technique for denoising 3D Magnetic Resonance
Spectroscopic Imaging (MRSI) data. Our proposed method involves a novel
spectral de-phasing and re-phasing approach which increases the phase dimension
of the spectra to deal with the arbitrary complex phase in the data. This is
coupled with an anisotropic non local means (NLM) filter-based pattern-recognition across the multi-slice data to select similar spectra patches having a
similar phase for denoising. We show that our method leads to a mean SNR
improvement by an average factor of 4.5 while preserving the spectral resolution
of the metabolites.
PURPOSE
Magnetic Resonance Spectroscopic
Imaging (MRSI) is a clinical imaging tool which is used for generating
metabolic maps of tissues in-vivo. However, long acquisition times, poor SNR
and low spatial resolution often lead to poor metabolic quantification.
Conventional denoising-methods such as apodization, wavelet transforms4 and NLM1,3 do not work effectively as they induce smoothing artifacts and
do not account for the arbitrary complex-phase induced in the spectra during
acquisition. This work proposes a
spatially-adaptive denoising of 3D-MRSI data by using a frequency-phase NLM1,3
technique. A multi-slice data, having not more than 3 successive
slices to avoid significant changes in the MR spectra data, would increase the redundant
spectral information available as compared to a single-slice data. The main
contributions of our method are: 1) robustness to arbitrary phase-shifts as the
phase-angles range from $$$[0,2\pi]$$$ for all spectral signals, and 2)
adaptive to the multi-slice imaging-data as the spectra are denoised by relying on similar
signals with a similar phase instead of pre-defined prior
assumptions.METHODS
Spectral Dephasing: The complex spectra in each voxel underwent a phase-shift by a pre-defined set of phase-angles $$$[0,2\pi]$$$. This increased the phase-dimension of
the spectra thereby generating a 2D frequency-phase space (Figure 1). Spectral patches from this space were then extracted for denoising.
$$S^\Theta(\omega) = \mathcal{F}(S(t)*e^{-i\Theta})$$
Anisotropic NLM: An anisotropic
variant of the NLM1,3 was used
to search spatially for similar spectral-patches with similar phase across the 3-slices but for a specific metabolite-frequency. The patch-size used was: $$$1\times1\times1$$$ and $$$3\times3\times3$$$, with the search
region size: $$$\forall$$$ voxels x $$$\forall$$$ angles x $$$\forall$$$ slices. A weighted average of all similar patches was
taken to give a denoised patch – a patch with higher
similarity was assigned a higher weight.
$$S_1^\Theta(\omega) =NLM(S^\Theta(\omega))$$
Spectral Rephasing: After obtaining the
denoised frequency-phase spectral space for each voxel, an inverse phase-shift
was performed to reverse the effects of dephasing. The spectra generated were
then averaged to obtain a single, complex denoised spectra.
$$S_1^\Theta(t) =\mathcal{F}^{-1}(S_1^\Theta(\omega))$$
$$\hat{S}(\omega) = \mathcal{F}(S_1^\Theta(t)*e^{i\Theta}),\forall\Theta$$
Data acquisition: We tested our
method on a 3D brain MRSI data of a healthy human volunteer using a 3T-750w
system (GE-Healthcare) with a 12-channel head receive coil. PRESS localization,
CHESS water suppression and EPSI readout were used as part of the sequence. The
acquisition parameters used were: FOV = $$$220\times220\times80$$$ mm3, voxel size = $$$10\times10\times10$$$ mm3, TE/TR
= 144/1000
ms and spectral bandwidth = 1kHz and 8 slices. The acquired
data was zero-filled and reconstructed to generate a grid of $$$40\times40$$$ voxels and
400 spectral points. The test data used were: single-slice 2D and three
successive slices of the 3D data with 3 averages.
RESULTS
The SNR of the different metabolites was calculated as the ratio
between the maximum value of the real metabolite peak respectively, versus the
standard deviation of the noise signal at the negative end of the ppm-scale
after baseline correction. The spectral-resolution (measured by calculating the
Full-Width Half Maximum (FWHM) of the water peak) and
concentration-estimates of the metabolites were measured using the LCModel2. Figure 3 shows the SNR maps for the original, the single slice and multi-slice data post-frequency-phase NLM while Table 1 shows the corresponding
SNR values.
Table 2 evidences the improvement in concentration estimates and
reduction in standard-deviation error after applying our method.DISCUSSION
We account for different spectral phase-angles and apply the proposed method to denoise the data. While there may be a risk of incorporating spectra from other slices, our pattern-recognition method
successfully avoids this by assigning higher weights to similar-spectra. This is evident by the lack of contamination in the CSF or any
abnormal increase in concentration-estimates. Figure 2 shows the
original and denoised spectra for sample voxels using the proposed method while
Figure 3 shows the SNR-maps for NAA, Cho and Cr. The multi-slice data exhibits a higher improvement in SNR than the single-slice data due to more
redundant spectral information available from multiple-slices. The improvement in
mean-SNR for all major metabolites while preserving the FWHM (Table 1)
indicates a consistent performance by our method. Table 2 shows an
improvement in concentration-estimates for NAA, Cho and Cr and a reduced
standard deviation-error after applying frequency-phase NLM. CONCLUSIONS
We propose a denoising method for multi-slice
3D-MRSI data using anisotropic-NLM and
show the added benefit of incorporating complex phase information in the
patches and using redundant information from successive slices for denoising.
This enables a mean-SNR improvement of approximately 4.5 while retaining spectral-resolution and improving the concentration-estimates of the metabolites. Further improvements would involve using computationally-efficient
methods to improve the implementation speed and quantify lower-concentration
metabolites.Acknowledgements
The research leading to these results has received funding from the European Union's H2020 Framework Programme (H2020-MSCA-ITN-2014) under grant agreement no. 642685 MacSeNet.References
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