Yannick Brackenier1,2,3, Thomas Wilkinson1,2,3, Lucilio Cordero-Grande1,2,4, Raphael Tomi-Tricot1,2,3,5, Philippa Bridgen1,2,3, Sharon Giles1,2,3, Enrico De Vita1,2,3, Shaihan J Malik1,2,3, and Joseph V Hajnal1,2,3
1Biomedical Engineering Department, School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom, 2Centre for the Developing Brain, School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom, 3London Collaborative Ultra high field System (LoCUS), London, United Kingdom, 4Biomedical Image Technologies, ETSI Telecomunicación, Universidad Politécnica de Madrid and CIBER-BNN, Madrid, Spain, 5MR Research Collaborations, Siemens Healthcare Limited, Frimley, United Kingdom
Synopsis
DISORDER is an established retrospective data driven motion correction approach that uses optimised phase encoding, but otherwise unmodified 3D acquisitions. It is highly effective, but requires multiple lines of k-space to be grouped together for each motion state to be estimated, and this limits temporal resolution. At 7T, head motion can also be detected by “Pilot Tone”, which is an injected RF signal picked up by each coil in the head receiver array, but a calibration step is required. Here we combine DISORDER and Pilot Tone to achieve integrated calibration and show that improved motion correction can result.
Introduction
Brain MRI is susceptible to motion which causes artefacts
in reconstructed images1, especially with prolonged scanning times for high-resolution
MRI, particularly relevant at ultra-high field (UHF)2. Data-driven motion
correction proposed in DISORDER3,4 leverages an optimised Cartesian sampling
to retrospectively correct for rigid body motion during volumetric acquisitions.
Whilst able to correct UHF acquisitions5, stable motion estimates require multiple
readout lines to be assigned to a single motion state, limiting the temporal
resolution of estimates. In this work, we extend DISORDER motion estimation by
incorporating external motion information coming from injected Pilot Tone (PT) signals6 potentially improving the temporal resolution of motion
estimates.Methods
DISORDER
motion correction3,4 divides the k-space acquisition into temporal groups
(sweeps) of readouts (one per repetition time TR) that sample uniformly across k-space. Each sweep $$$n$$$ is treated as a different motion state with
rigid motion parameters $$$\textbf{z}_n$$$ that can be jointly optimised together
with the image $$$\textbf{x}$$$:
$$(\widehat{\textbf{x}},\widehat{\textbf{z}_n})=argmin_{\textbf{x},\textbf{z}_n}\sum_q\Big\| \textbf{A}_q\textbf{FST}(\textbf{z}_q)\textbf{x}-\textbf{y}_q \Big\|_2^2 \quad\quad(1)$$
where $$$q$$$ is the running variable summing over all sweeps with $$$\textbf{T}(\textbf{z}_q)$$$,$$$\textbf{S}$$$,$$$\textbf{F}$$$,$$$\textbf{A}_q$$$ and $$$\textbf{y}_q$$$ respectively representing associated rigid motion, coil
sensitivities, Fourier operator, sampling structure, and measured k-space data. PT is a motion-estimation method leveraging signals collected
during data acquisition by each receiver channel from an externally generated mono-frequency
RF source: PT signals vary slightly with head position and provide updated
motion information with every TR6,7. For brain MRI at 7T, it was shown that a linear model can be used to predict motion parameters ($$$\textbf{z}_{{TR}_t}$$$) from the PT signal ($$$\textbf{p}_{{TR}_t}$$$)8:
$$\textbf{z}_{{TR}_t}=\textbf{C}\textbf{p}_{{TR}_t}\quad \quad(2)$$
where $$$\textbf{p}_{{TR}_t}$$$ is a 33-element
complex vector containing 32-channel PT signal for the TR at time $$$t$$$ and a 1 to allow for motion offsets. $$$\textbf{C}$$$
is a 6x33 matrix with coefficients for each of the 6 rigid motion
parameters in each row. This allows estimating $$$\textbf{C}$$$:
$$(\widehat{\textbf{x}},\widehat{\textbf{C}})=argmin_{\textbf{x},\textbf{C}}\sum_q\Big\|\textbf{A}_q\textbf{FST}(\textbf{C}\textbf{p}_{q})\textbf{x}-\textbf{y}_q \Big\|_2^2 \quad \quad(3)$$
where $$$\textbf{p}_{q}$$$ is the averaged PT signal within the time window $$$w_q$$$ of shot $$$q$$$. Whereas in Equation 1 each motion state is
estimated by optimising for an independent quantity, the matrix $$$\textbf{C}$$$ is assumed to be constant for the full
acquisition, which can stabilise motion states over time. Implementation details for solving Equation 3 are shown in Figure 2.
The
proposed reconstruction was tested in simulations and validated on 4 healthy
volunteers (HV) (aged 25-35yrs, Institutional Research Ethics number
HR-18/19-8700) with a mix of deliberate motions and lying still, using a
volumetric SPGR acquisition on a 7T scanner (MAGNETOM Terra, Siemens
Healthcare, Erlangen, Germany). Sequence parameters: $$$0.5^3mm^3$$$ isotropic resolution, DISORDER random
checkered sampling with $$$4.1s$$$ per sweep, $$$TR=8.4ms$$$, echo time $$$TE=4.2ms$$$, flip
angle $$$FA=7^{\circ}$$$, field of view (FOV)=248x238x176
(IS/AP/RL), readout along
IS, scan duration $$$TA=19min49s$$$ with no repeats and no acceleration. The PT was
generated with an RF signal generator (APSIN3000, AnaPico, Glattbrugg,
Switzerland) and broadcast into the magnet room from a monopole
antenna at a drive level of $$$-20dBm$$$ (Figure 1a) and
with an offset to set the signal in the oversampled FOV, which was extracted
before removing the oversampling (Figure 1b). Images
are first reconstructed using motion parameters obtained from solving Equation
1 and $$$\textbf{C}$$$
was then calibrated using Equation 2 to obtain
the final reconstructions from the PT consistent motion parameters. Due to computational
constraints, full volumetric data was reconstructed at $$$1mm^3$$$ and the motion information (either temporal
motion estimates or the calibrated matrix
) was then used to
reconstruct single slabs at $$$0.5^3mm^3$$$.
Results
Figure 3a shows the estimated motion parameters with
DISORDER compared to PT predicted motion states. These agree well overall, with
cleaner estimates using the PT calibration. Zoomed-in traces (Figure 3b) show
the higher temporal resolution motion estimates PT provides (per TR). Example reconstructed
images in Figure 4 show successful motion correction using DISORDER, but further
improvements using the PT predicted motion information. PT reconstructions for
all subjects showed either similar or improved image quality compared to
DISORDER.Discussion
We have investigated and integrated PT signals to improve
DISORDER motion correction. PT signal calibration can be achieved using the
DISORDER motion states and the two then show a strong correlation, but the PT estimates
are more stable and have higher temporal resolution. Replacing DISORDER motion
estimates with PT either produced similar results or improved motion
correction. As shown in Figure 3, PT can provide per TR motion estimates, which
look highly coherent. It seems plausible that motion correction at the TR level
could yield further improvements but this has hitherto proved computationally infeasible with the current framework. Conclusion
We have exploited the use of PT at UHF to improve data-driven
motion correction. Our method does not interfere with sequence parameters and
can be used in almost any sequence.
PT predicted motion states can improve image quality and offer new ways to retrospectively
detect and correct for motion at a higher temporal resolution, potentially with individual motion
states for each k-space line (i.e. at the TR level).
Acknowledgements
The authors would like to thank Francesco Padormo for the loan of
the RF signal generator.
This work was funded by the
King’s College London & Imperial College London EPSRC Centre for Doctoral
Training in Medical Imaging [EP/L015226/1] and supported by a Wellcome Trust
Collaboration in Science Award [WT 201526/Z/16/Z] and the Wellcome/EPSRC Centre
for Medical Engineering [WT 203148/Z/16/Z].
This work was supported by Wellcome Trust Collaboration in Science
grant [WT201526/Z/16/Z] and by the National Institute for Health Research
(NIHR) Biomedical Research Centre based at Guy’s and St Thomas’ NHS Foundation
Trust and King’s College London and/or the NIHR Clinical Research Facility. The
views expressed are those of the author(s) and not necessarily those of the
NHS, the NIHR or the Department of Health and Social Care.
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