Johannes Breitling1,2,3, Anagha Deshmane4, Steffen Goerke1, Kai Herz4, Mark E. Ladd1,2,5, Klaus Scheffler4,6, Peter Bachert1,2, and Moritz Zaiss4
1Division of Medical Physics in Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany, 2Faculty of Physics and Astronomy, University of Heidelberg, Heidelberg, Germany, 3Max Max Planck Institute for Nuclear Physics, Heidelberg, Germany, 4High-field Magnetic Resonance Center, Max Planck Institute for Biological Cybernetics, Tübingen, Germany, 5Faculty of Medicine, University of Heidelberg, Heidelberg, Germany, 6Department of Biomedical Magnetic Resonance, Eberhard-Karls University Tübingen, Tübingen, Germany
Synopsis
Chemical exchange saturation transfer (CEST) MRI
allows for the indirect detection of low-concentration biomolecules by their saturation
transfer to the abundant water pool. However, reliable quantification of CEST
effects remains challenging and requires a high image signal-to-noise ratio. In this study, we show that principle component
analysis can provide a denoising capability which is comparable or better than
6-fold averaging. Principle component analysis allows identifying similarities
across all noisy Z-spectra, and thus, extracting the relevant information. The
resulting denoised Z-spectra provide a more stable basis for quantification of
selective CEST effects, without requiring additional measurements.
Introduction
Chemical exchange saturation transfer (CEST) MRI
allows for the indirect detection of low-concentration biomolecules by their saturation
transfer to the abundant water pool. However, quantification of inherently
small CEST effects remains challenging and requires high image signal-to-noise
ratio (SNR) to achieve reliable results. For optimized saturation parameters
and image readout, higher SNR can only be achieved by averaging, resulting in prolonged
measurement times. In this study, principle component analysis (PCA) was utilized
to identify similarities across all Z-spectra, extract the relevant information
i.e. principal components (PCs) and reduce the dimensionality to improve the
SNR without averaging.1,2
Methods
The proposed denoising algorithm (Fig. 1) is applied
after motion correction using a rigid-registration-algorithm
in MITK3, normalization, correction of B0-inhomogeneities,
and segmentation of brain tissues (cerebrospinal fluid, gray matter, and white
matter). CEST data, consisting of images of size
$$${u}\times{v}\times{w}$$$ for the $$$n$$$ saturation frequency offsets, is
reshaped into a Casorati matrix
$$$\textbf{C}$$$ of size
$$$ {m}\times{n}$$$
, with $$${m}\leq{u}\cdot{v}\cdot{w}$$$
being the
number of brain voxels. Each row of
$$$\textbf{C}$$$ represents the
Z-spectrum of one voxel and each column represents a complete segmented image
for one saturation frequency offset.
PCA is performed by eigendecomposition of the
covariance matrix
$$\mathrm{cov}(\textbf{C})=\frac{1}{n-1}\widetilde{\textbf{C}}^\textbf{T}\widetilde{\textbf{C}}$$
$$\quad=\bf\Phi^\textbf{T}\Lambda\Phi$$
with
$$$\widetilde{\textbf{C}}$$$ being the
column-wise mean-centered Casorati matrix,
$$${\bf\Phi}=({\bf\varphi}_1{\bf\varphi}_2\ldots{\bf\varphi}_n)$$$ being the
$$${n}\times{n}$$$ orthonormal
eigenvector matrix and $$${\bf\Lambda}=\mathrm{diag}(\lambda_1,\lambda_2,\ldots,\lambda_n)$$$ being the
associated diagonal eigenvalue matrix with
$$$\lambda_1\geq\lambda_2\geq\cdots\geq\lambda_n$$$
. The variance i.e. information content of a signal
will concentrate in the first few PCs, whereas the noise is spread evenly over
the dataset. Therefore preserving the first few PCs will remove noise from the
data set. The optimal number of components
can be determined
by an empirical indicator function applied to the eigenvalues.4
$$k=\underset{i}{\mathrm{argmin}}\left[\frac{\sum_{l=i+1}^{l=n}\lambda_l}{m(n-i)^5}\right]^\frac{1}{2}$$
Projection of
$$$\widetilde{\textbf{C}}$$$
onto the reduced set of the first $$$k$$$ eigenvectors
$$${\bf\Phi}_{(k)}$$$
$$\widetilde{\textbf{C}}_{(k)}=\widetilde{\textbf{C}}{\bf\Phi}_{(k)}{{\bf\Phi}_{(k)}}^\textbf{T}$$
and addition of the mean Z-spectrum results in the denoised Casorati
matrix. Denoised Z-spectra are reformatted into a final denoised image series
with dimensions $$${u}\times{v}\times{w}\times{n}$$$.
In vivo 3D-CEST-MRI
(1.7×1.7×3 mm3, 12 slices) was performed on a 7T whole-body scanner
(Siemens Healthineers, Germany) using the snapshot-CEST approach5.
Pre-saturation by 140 Gaussian-shaped pulses (tp = 15 ms, duty cycle
= 60%, tsat = 3.5 s) was applied at 54 unevenly distributed offsets for
two different mean B1 = 0.6 and 0.9 µT. Each Z-spectrum was acquired
six times to enable comparison with high-SNR data obtained by averaging. Conventional,
averaged and denoised Z-spectra were fitted pixel-wise with a Lorentzian 5-pool
fit model. Lorentzian difference images were calculated according to $$$\mathrm{MTR_{LD}}=Z_{ref}-Z$$$ and corrected for B1-inhomogeneities6.
Results
Considerable noise is
observed in the unprocessed Z-spectra (Fig. 2 left). Averaging 6 measurements reduces
the noise significantly, allowing reliable identification of CEST resonances
(Fig. 2 middle). The same resonances are also revealed by application of the
denoising algorithm, indicating the correct choice for the number of components
(Fig. 2 right). The smoother overall appearance of the denoised vs. averaged
Z-spectra suggests the algorithm is equivalent or better than averaging. This
result is also apparent in the APT and rNOE MTRLD contrasts calculated from
denoised Z-spectra, which exhibit comparable or better image quality than those
from averaged spectra (Fig. 3).Discussion
PCA was previously shown to be a powerful denoising
technique in HyperCEST, with the optimal number of components deduced from the composition
of the investigated phantom.2 For conventional CEST experiments, the number
of relevant components is not straightforward to determine, as the number of contributions,
their dependencies on physiological parameters and pathological alterations
thereof are unknown. If too few components are preserved, resonances would be
missing or deformed; too many components would diminish the denoising
performance. In this study, the optimal number is determined using a
data-driven approach4, the functionality of which was verified by the similarity
of averaged and denoised Z-spectra.
Prior segmentation and correction for B0
inhomogeneities ensured only relevant i.e. meaningful voxels with the same
spectral position were included. PCA generally requires a sound statistical
basis (i.e. a large number of voxels) to determine the PCs whereas the
denoising performance itself depends on the number of preserved components. Therefore
the denoising approach will benefit from 3D imaging, especially whole-brain
imaging, and from a large number of acquired offsets.Conclusion
PCA denoising of Z-spectra
results in contrasts which are comparable or even superior to those achieved by
averaging. With this technique at hand, small CEST effects can be reliably
quantified without the need for additional measurements. This might allow clinical
application of CEST MRI at low field strengths as well as with fast imaging
sequences by compensating for the expected SNR deterioration.Acknowledgements
Max Planck Society (support to JB, MZ, AD); German
Research Foundation (DFG, grant ZA 814/2-1, support to MZ); European Union
Horizon 2020 research and innovation programme (Grant Agreement No. 667510,
support to MZ, AD).References
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