Charles John Marchini1 and Brad Sutton 1
1Bioengineering, University of Illinois Urbana-Champaign, Urbana, IL, United States
Synopsis
ASL methods result in low SNR. SVD denoising can be used to
increase the temporal SNR of ASL data by throwing out the low energy singular values. The SVD can be done after a standard reconstruction, or as we show here
during the reconstruction if partial separability is used. The incorporation of
the SVD into the reconstruction algorithm allows for a higher tSNR within the
gray matter. It also paves the path for future work in which subsampling the
data results in higher temporal and spatial resolution ASL.
Introduction
ASL has a low temporal SNR (tSNR), limiting its potential for high spatial and temporal resolution imaging. From a singular value decomposition (SVD) of perfusion data, it becomes apparent that the low rank components corresponding to the large singular values contain the perfusion information, and the high rank components corresponding to the lower energy singular values consist mainly of noise. Denoising utilizing SVD can be accomplished in several ways, first, retrospectively by taking the standard ASL reconstruction and removing the lower energy singular values. Second, using the partial separability (PS) model, the SVD can be built into the reconstruction algorithm. This allows for more complicated sampling patterns including subsampling of the data1.The PS model acquisition works by sampling a temporal navigator signal interleaved with an imaging data acquisition. The right singular vectors (RSVs) of the navigator, a signal with a high temporal resolution and low spatial resolution, is used as the estimate of the temporal signals in the data. To estimate the spatial maps for those components, the conjugate gradient algorithm is used to fit the SVD reconstruction to the high spatial resolution data collected, as has been done with BOLD fMRI2 and speech imaging3,4.Methods
A 3D stack of spirals was used for a FAIR PASL 3D
acquisition of imaging data combined with a short 3D spiral for the temporal
navigator. The nonuniform fast Fourier transform algorithm was used to accommodate
the non-uniform sampling in the frequency domain in the reconstruction5. The
data consisted of 16 spirals, each spiral corresponding to a point in the Kz
axis as shown in Figure 1, fully sampling k-space. The voxel sizes were
3.8x3.8x6mm, the image dimensions were 64x64x16, and the TR was 5 seconds. 40 tag-control
pairs were taken. The first pair did not include background suppression for
calibration purposes, and the last 39 did include background suppression. Data
were reconstructed in two ways: 1. Standard reconstruction with conjugate
gradient method applied to the k-space data of each volume. 2. PS model
reconstruction for the entire time series at once.
The singular value decomposition of the navigator data was
taken, and a conjugate gradient algorithm was used to fit the spatial basis to
the data using the temporal basis from the navigator according to the PS model
equation:
$$c_l(k)=arg\min_{c_l(k)}||s(k,t)-\sum_{l=1}^Lc_l(k)\rho_l(t)||^2$$
where $$$L$$$ is the rank of the reconstruction, $$$t$$$ is the time point (tag/control), $$$c_l(k)$$$ is the estimated spatial basis (principal
components including singular values), $$$s(k,t)$$$ is the acquired data, and $$$\rho_l(t)$$$ is the estimated temporal basis (RSVs of the
navigator data).
For the PS reconstruction, 9 iterations
were taken with a rank of 10 to reconstruct all time points together. For the
standard reconstruction, 10 iterations of the conjugate gradient algorithm were
used to reconstruct each time point volume.
The perfusion images were acquired by pairwise
subtraction of the last 39 of the tag-control pairs and were thresholded at
zero signal. The tSNR measurements were found by pixel-wise averaging of the
perfusion signal across time divided by the standard deviation of the perfusion
signal across time.
The gray matter tSNR measurements were
computed by first manually brain extracting with the sensitivity maps as the
template, then using the gray matter partial volume as found with FSL6 thresholded at 0.5 to segment gray matter voxels in the tSNR maps which were
used for the calculation. An example of a segmented slice is shown in Figure 2.
Results
The perfusion images resulting from the reconstruction are
shown in Figure 3 for both the PS reconstruction and the standard reconstruction,
with the standard reconstruction being based on an ASL consensus paper7.The
temporal signal to noise ratio (tSNR) was compared for the PS reconstruction
and the standard reconstruction (Figure 4a,b), and between the PS reconstruction
and the standard reconstruction with post processing SVD denoising (Figure 4c,d). The
gray matter tSNR measurements were 1.56 with standard deviation 1.34, 0.89 with
standard deviation 0.62, and 1.34 with standard deviation 1.24 for the PS
reconstruction, standard reconstruction, and standard reconstruction with SVD
denoising, respectively.Discussion
From the tSNR comparisons, the use of the SVD to remove
noise improves the tSNR of the standard reconstruction when applied after
reconstructing the image. Further, when incorporated into the PS model, the low
rank reconstruction can provide further improvements in tSNR in the gray
matter. The tSNR may be slightly higher in the PS reconstruction because the
model restriction improves the conditioning of the reconstruction problem for
the PS model over individual reconstructions of each image in the standard
approach. Future work will include subsampling the data, allowing for an
increased temporal and spatial resolution. An example of a subsampling data
acquisition is shown in Figure 5.Conclusion
The PS model allows for the SVD denoising to be built into the reconstruction algorithm. This improves the tSNR
of the ASL data even over retrospectively applied SVD after a standard
reconstruction. Future work should show that this allows for subsampling of the
data, and increased temporal and spatial resolution.Acknowledgements
This work was supported by the Miniature Brain Machinery
Fellowship, training grant number NSF 1735252References
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