Amir Seginer1, Graeme A. Keith2, David A. Porter2, and Rita Schmidt3
1Siemens Healthcare Ltd, Rosh Ha'ayin, Israel, 2Institute of Neuroscience and Psychology, University of Glasgow, Glasgow, Scotland, 3Department of Brain Sciences, Weizmann Institute of Science, Rehovot, Israel
Synopsis
Readout-Segmented COKE (RS-COKE) is an Echo Planar
Spectroscopic Imaging (EPSI) variant supporting larger spectral-widths and is therefore
useful for spectral imaging at 7T. However, mismatches between the segments at
the overlaps lead to artifacts, especially if the lipids signal is not
suppressed (to avoid adversely affecting the metabolites signal). We developed
a procedure to measure and reduce the readout segment mismatches – through
signal and trajectory corrections – leading to improved spectral images and
spectra. The procedure was tested by
scanning both a special 3D head-shaped phantom – which includes a lipid layer –
and human volunteers.
Introduction
RS-COKE (Readout-Segmented COnsistent K-t space
Eᴘsɪ)1
is an EPSI (Echo Planar Spectroscopic
Imaging) variant offering increased spectral width (SW) and is thus especially
promising for spectral imaging of human brain metabolites at 7T. The increased
spectral width is achieved both by readout segmentation2 — allowing
shorter echo-spacing — and by the COKE scheme3,4 that ensures all
same-phase-encode (PE) acquisitions use same-sign readout (RO) gradients —
halving the effective dwell time to a single echo-spacing. In practice, COKE
switches the N/2 Nyquist ghost artifacts from the temporal domain to the PE
domain where they are more benign.
RS-COKE is, however, susceptible
to image artifacts from mismatches between readout segments. Artifacts are
especially pronounced when lipid suppression is off (to avoid adversely
affecting the metabolites signal). In this study, we developed a procedure to
measure and reduce the RO-segment mismatches, leading to improved spectral
images and spectra. Corrections included i) frequency-dependent phase
corrections; ii) a correction of the trajectories used by the reconstruction;
and iii) a gradual transition between segments to smooth any residual
mismatches. The corrections were verified on a special head-mimicking phantom,
and on human volunteers.Methods
Sequence/Acquisition
Figure 1 shows the RS-COKE pulse
sequence, implemented on a 7T MAGNETOM Terra (Siemens Healthcare, Erlangen,
Germany). It is readout segmented and employs sine-shaped readout gradients.
The COKE scheme adds alternating PE blips between the RO gradients, reversing
the sign of both PE blips and RO gradients every excitation, to achieve the
trajectories shown. A VAPOR water-suppression module is included, as is a refocusing
pulse, but no lipid suppression.
The sequence also includes three
reference scans on water. The first, a conventional N/2 Nyquist ghost
calibration with no PE gradients. Two additional scans, also with no PE
gradients, are acquired for calibrating the trajectories. These are acquired at
two adjacent RO segments with an additional prepended RO prephaser shifting
both segments to overlap around $$$k_x=0$$$, where the signal is
maximal.
A separate gradient-echo (GRE) scan on water is used to calibrate
the complex coil-combination weights per voxel.
Reconstruction
The basic reconstruction steps were:
-
Time apodization
(exponential with decay constant of 0.1 s).
-
Hann filtering of all k-space dimensions.
-
Fourier transform (FT) of all dimensions, using
regridding along the non-uniformly sampled RO direction.
-
An optimized linear coil combination,5
using complex weights derived from the water GRE calibration scan.
Off-Resonance Reconciliation
To resolve off-resonance
phase differences along readouts employing opposite gradients, an FT along the time
domain was applied (prior to re-gridding) and the linear phase per frequency
(and per gradient-sign) was removed. To ensure phase continuity at segment
joins, an additional phase — per-segment and per-frequency — was added to each
readout.
Segment Trajectory Corrections
The ideal $$$k_x$$$ trajectory of segment $$$s$$$, sampled at time $$$t_n$$$ is given by $$k_x^{(s)}(t_n)=k_{x,\text{ideal}}^{(s=0)}(t_n)+s\cdot\Delta{k}_{\text{seg}},$$ where $$$\Delta{k}_{\text{seg}}$$$ is the $$$k_x$$$ shift between segments. This was
replaced by a parametrized trajectory with extra tuning parameters $$$\eta$$$ and
$$$\tau$$$ $$k_x^{(s)}(t_n)=\eta\cdot{k}_{x,\text{ideal}}^{(s=0)}(t_n+\tau)+s\cdot\Delta{k}_{\text{seg}}$$ or, for the reference scans
(the same with an extra $$$+\Delta{k}_{\text{ref}}$$$ to center the overlap around $$$k_x=0$$$)
$$k_x^{(s)}(t_n)=\eta\cdot{k}_{x,\text{ideal}}^{(s=0)}(t_n+\tau)+s\cdot\Delta{k}_{\text{seg}}+\Delta{k}_{\text{ref}}.$$ The parameters $$$\eta$$$ and $$$\tau$$$ were tuned so that odd signals of the
trajectory reference scan (acquired during positive gradients) best match at
the segments’ overlap — see figure 2. The even trajectories were further
updated according to the N/2 Nyquist reference scan. The corrected trajectories
were then used in the regridding.
To further reduce artifacts, from
residual inter-segment inconsistencies, transitions were also smoothed during
the regridding process, effectively averaging the signals with linearly varying
weights along the overlap. This was achieved by scaling the regridding
sample-weights within the overlap — found for each segment separately — by $$$f$$$ for one segment and $$$(1-f)$$$ for the other, with $$$f$$$ varying along the overlap from 0 to 1;
linearly dependent on $$$k_x$$$. See figure 3.
Phantom
A 3D-printed head-shaped phantom designed for 7T
was used.
5 It included an agar “brain” with metabolites and an oil
filled “lipid” layer.
Scan parameters
Scan parameters for the phantom were: TR/TE 2000/14.6 ms,
FOV (RO×PE) 200×250 mm
2, slice thickness 20 mm, in-plane resolution 4.17×3.9
mm
2 (48×64 acquisition matrix), 3 readout segments, SW 2778 Hz, echo spacing
0.360 ms, 294 echoes, and scan duration 6:32 min.
For human imaging the scan parameters were: TR/TE 1600/13 ms, FOV (RO×PE)
260×300 mm
2, slice thickness 15 mm, in-plane resolution 4.12×4.69 mm
2 (63×64
acquisition matrix), 3 readout segments, SW 2778 Hz, echo spacing 0.360 ms, 638
echoes, and scan duration 5:14 min.
Results
Figure 4 shows phantom results; showing NAA, Cr, and Cho
images as well as spectra at two representing points. Results are shown with
and without trajectory corrections. Figure 5, shows the same for the human
imaging.Discussion & Conclusions
Readout segmented acquisition is prone to artifacts
from segment inconsistencies, artifacts are exacerbated by the lipids' strong
signal, if lipid suppression is off. These artifacts were reduced by using a
reference scan based trajectory correction, smoothing of the signal at segment
transitions, as well as — per-frequency and per-segment — phase corrections.
The in vivo images still occasionally suffer from some artifacts, which are
most likely due to motion and breathing. Full analysis still requires phasing
of all data and model fitting of the spectra.Acknowledgements
No acknowledgement found.References
-
Keith
GA, Seginer A, Porter DA, Schmidt R, Echo-planar spectroscopic imaging
with readout-segmented COKE at 7T: Artifact analysis using a purpose-built
phantom and simulation. In: Proceedings of the 29th Annual Meeting of
ISMRM, 2021.
- Keith
GA, Vicari M, Woodward RA, Porter DA, In vivo echo-planar spectroscopic
imaging (EPSI) at 7 tesla with readout segmentation for improved spectral
bandwidth. In: Proceedings of the 27th Annual Meeting of ISMRM. Montréal,
QC, Canada, 2019.
- Webb
P, Spielman D, Macovski A. A fast spectroscopic imaging method using a
blipped phase encode gradient. Magnetic Resonance in Medicine
1989;12:306–315.
- Schmidt
R, Seginer A, Tal A. Combining multiband slice selection with consistent
k-t-space epsi for accelerated spectral imaging. Magnetic Resonance in
Medicine 2019;82:867–876.
- Jona G, Furman-Haran E, Schmidt R. Realistic head-shaped phantom with
brain-mimicking metabolites for 7 t spectroscopy and spectroscopic imaging. NMR
in Biomedicine 2021;34:e4421.