Ricardo P. Martinho1, David Koprivica1, Mihajlo Novakovic1, Michael J. Jaroszewicz1, and Lucio Frydman1
1Department of Chemical and Biological Physics, Weizmann Institute of Science, Rehovot, Israel
Synopsis
2D MRI/S are commonly affected by changes
in temperature, field drifts, or motions, leading to multiplicative noise. We
introduce here CoSeM (Compressed Sensing Multiplicative) denoising, a method
that converts instability-related “t1” noise, into additive noise
liable to signal averaging. CoSeM evaluates and discards indirect-domain points
that may have been strongly influenced by instabilities, and makes up for this
discarding by compressed sensing reconstructions. 2D localized MRS in the brain
and 2D abdominal MRI experiments liable to instabilities, evidence 2-3 fold
increases in SNR by CoSeM processing. CoSeM is also shown to retain
quantitative information –e.g., in T1 mapping experiments.
Introduction
MRI and MRS toolboxes provide a multitude of anatomical and dynamic information. However, such experiments usually span several dimensions acquired over protracted times, that make them susceptible to temperature alterations, field-related frequency drifts, motions, etc.1-3 This well described problem in the in vitro and in vivo NMR literature is often denoted as t1 noise.1 Several approaches have been introduced to tackle it, such as pulse sequence modifications,4 reference-based denoising,5 signal co-addition,6 singular value decomposition,7 or resampling.8 The majority of these methods require high signal-to-noise ratio, can only be applicable to specific experiments, or can lead to false positive and/or false negative peaks, thus damaging the spectral quality itself. This study proposes CoSeM –a general method to improve the SNR of spectra and images corrupted by multiplicative noise, which uses sub-sampled datasets chosen to be minimally corrupted, and reconstructs them generating a spectrum/image by compressed sensing (CS9-12) –thereby attenuating the corrupted data’s influence. Methods
CoSeM denoising
is a custom script written on Matlab, calling the BART Toolbox13 for
the CS implementation. In vivo 2D localized MRS experiments were
performed in naïve black mice in a 15.2 T Bruker; abdominal MRI experiments
were performed on orthotopic KPC pancreatic tumor-bearing mice in a 7.0 T Agilent.
See Captions for further details. Results
Multiplicative
noise manifests itself in nD MRI/S as pseudo-random variations along the
baseline of the indirect dimension(s). This convolves the legitimate signal
with spectral instabilities, which in the Fourier domain is expressed as:
S(ω1,ω2) = A(ω1)ω1 Strue*(ω1,ω2)
n1 indirect-domain points will thus be associated with n1 different
coefficients of {A}, describing fluctuations ≠1.
It is in principle possible to reduce the number of coefficients and still
reconstruct the 2D data via compressed sensing, by taking a sub-representation
of the fully sampled data set where a fraction of the sampled k/t1
values along the indirect domain, has been randomly masked out. This is the
underlying principle of CoSeM, which iterates these representations a number of
times (each with a different mask) leading to different ω1 noise patterns. CoSeM
then selectively co-adds these spectra/images, while using criteria that diminish
the amount incoherent noise, as sketched in Figure 1.
Figure 2
exemplifies the method on 2D localized double-quantum-filtered COSY experiments
collected on a live mouse brain. These acquisitions’ SNR is commonly dominated by
t1-noise and instabilities.14 Two criteria were used for guiding CoSeM’s selective averaging, based on
norm and entropy criteria. An average 3x increase in SNR is provided by either
criterion over the original data, performing significantly better than the
1.4-fold improvement obtained by blind-averaging. In no cases were spurious
cross-peaks originated by the method.
Figure 3 presents denoising
results attained in in vivo abdominal mice EPI MRI –a notoriously challenging
case affected by motions which can render EPI to be of limited value. As can be
seen, CoSeM significantly improves the image quality. This is best evidenced by
the slices displayed in (c-d), where less pronounced noise effects are seen both
in tissue-containing and tissue-free regions, while the edges of the tissues
are preserved with minimal blurring.
An important issue of
denoising methods concerns their preservation of quantitativeness: if this is
not kept, measurements of signal intensities will become compromised. CoSeM’s
faithfulness in this aspect was assessed by T1 values in the abdomen of a live
animal via inversion-recovery; then comparing the T1 maps obtained with and
without CoSeM. These results, are summarized in Figure 4, which evidences that
the method does not affect quantitativeness even when significantly changing
the signals’ intensities. Notice the improvement in SNR of the images, and the similarity
with the original image intensities evidenced by various organs (Fig. 4c).Discussion & Conclusion
Multiplicative
denoising by employing different random sampling and CS-based reconstruction
has been demonstrated in vivo for localized brain MRS and abdominal MRI.
This method shows generality and applicability to all these problems, in reasonably
low computational times. An SNR increase of 2-3 fold and no spurious signals
can be encountered in the spectra or images. Further work to applying these
methods to dynamical systems and increasing the dimensionality are ongoing.Acknowledgements
This work was supported
by the Clore Institute for High Field Magnetic Resonance Spectroscopy and
Imaging (Weizmann Institute), the Israel Science Foundation (grants 2508/17 and 965/18), a Thompson Family
Foundation grant, and the EU Horizon 2020 programme (Marie Sklodowska-Curie
Grant 642773). The authors thank Prof. Avigdor Scherz for providing the mice
with pancreatic tumors.References
- Mehlkopf,
A. F.; Korbee, D.; Tiggelman, T. A.; Freeman, R. Sources of t1 Noise in
Two-Dimensional NMR. J. Magn. Reson. 1984, 58, 315.
- Morris,
G. A. Systematic Sources of Signal Irreproducibility and t1 Noise in High-Field
NMR Spectrometers. J. Magn. Reson. 1992, 100, 316.
- Ladd,
M. E.; Bachert, P.; Meyerspeer, M.; Moser, E.; Nagel, A. M.; Norris, D. G.;
Schmitter, S.; Speck, O.; Straub, S.; Zaiss, M. Pros and Cons of
Ultra-High-Field MRI/MRS for Human Application. Prog. Nucl. Magn. Reson.
Spectrosc. 2018, 109, 1.
- Horne,
T. J.; Morris, G. A. Gradient-Enhanced Experiments P-Type COSY Show Lower t1
Noise than N-Type. Magn. Reson. Chem. 1997, 35, 680.
- Gibbs,
A.; Morris, G.; Swanson, A.; Cowburn, D. Suppression of t1 Noise in 2D NMR
Spectroscopy by Reference Deconvolution. Journal of Magnetic Resonance,
Series A. 1993, 351.
- Mo,
H.; Harwood, J. S.; Yang, D.; Post, C. B. A Simple Method for NMR t1 Noise
Suppression. J. Magn. Reson. 2017, 276, 43.
- Brissac,
C.; Malliavin, T. E.; Delsuc, M. A. Use of the Cadzow Procedure in 2D NMR for
the Reduction of T1 Noise. J. Biomol. NMR 1995, 6, 361.
- Song,
L.; Wang, J.; Su, X.; Zhang, X.; Li, C.; Zhou, X.; Yang, D.; Jiang, B.; Liu, M.
REAL‐ t1 , an Effective Approach
for t1 ‐Noise Suppression in NMR
Spectroscopy Based on Resampling Algorithm. Chinese J. Chem. 2020,
38, 77.
- Bostock, M.; Nietlispach, D.
Compressed Sensing: Reconstruction of Non-Uniformly Sampled Multidimensional
NMR Data. Concepts Magn. Reson. Part A 2017, 46A.
- Lustig, M.; Donoho, D. L.; Santos,
J. M.; Pauly, J. M. Compressed Sensing MRI: A Look at How CS Can Improve on
Current Imaging Techniques. IEEE Signal Process. Mag. 2008, 25, 72.
- Lustig, M.; Donoho, D.; Pauly, J. M.
Sparse MRI: The Application of Compressed Sensing for Rapid MR Imaging. Magn.
Reson. Med. 2007, 58, 1182.
- Chauffert, N.; Ciuciu, P.; Kahn, J.;
Weiss, P. Variable Density Sampling with Continuous Trajectories. SIAM J.
Imaging Sci. 2014, 7, 1962.
- Uecker, M.; Tamir, J. I.; Ong, F.;
Lustig, M. The BART Toolbox for Computational Magnetic Resonance Imaging. ISMRM
2016.
- Verma, G.; Hariharan, H.; Nagarajan, R.; Nanga, R. P. R.; Delikatny, E. J.;
Thomas, M. A.; Poptani, H. Implementation of Two-Dimensional L-COSY at 7 Tesla:
An Investigation of Reproducibility in Human Brain. J. Magn. Reson. Imaging
2014, 40, 1319.