Zhe Zhang1, Xiaodong Ma1, Erpeng Dai1, Hui Zhang1, and Hua Guo1
1Center for Biomedical Imaging Research, Department of Biomedical Engineering, School of Medicine, Tsinghua University, Beijing, China, People's Republic of
Synopsis
Multi-shot EPI can
achieve high resolution diffusion imaging, but the ghost artifacts caused by
shot-to-shot phase variations must be corrected. In recent works, k-space phase
correction methods have been proposed, which require navigator acquisitions for
each excitation for calibrating the k-space interpolation parameters. In this
work, a self-calibrated method for multi-shot DWI correction in k-space is
proposed, which does not require navigator acquisitions for efficient scanning
and does not suffer from the potential mismatch between image and navigator
echoes. Experiments on liver DWI demonstrate that the proposed method can correct the
motion induced artifacts in diffusion imaging.Purpose
Multi-shot
EPI (ms-EPI) can achieve higher resolution DWI than single-shot EPI (ss-EPI),
but the ghost artifacts caused by shot-to-shot phase variations must be
corrected. Some k-space correction methods for ms-EPI DWI have been proposed
1,2,3.
These methods explore the relationships among different shots, and use them for
k-space interpolation in an extended GRAPPA
4 (eGRAPPA) fashion to
recover the unacquired data. However, these methods require sequence with additional
navigator acquisition after the image echo, which prolongs the scan time. In this
work, a self-calibrated method for multi-shot DWI correction in k-space is
proposed, which does not require navigator acquisitions for efficient scanning
and does not suffer from the mismatch between image and navigator echoes
1,2,5.
This method is demonstrated with interleaved ms-EPI DWI in liver.
Methods
Reconstruction Recent works1,2,3
report the motion induced phase variations can be treated as a power of
encoding and k-space relationships among different shots are used for k-space eGRAPPA
interpolation. In these studies, additional navigator echoes are needed to
calculate the interpolation parameters, which prolongs the scan time by about
1/3. In this work, self-calibrated eGRAPPA is implemented as follows: 1) virtual
navigators are firstly generated by recovering the missing data in each shot using
the conventional GRAPPA4; 2) the calibration among shots is performed
from these calculated navigators followed by eGRAPPA interpolation as in previous
work1; 3) partial Fourier reconstruction and complex image
combination6 are performed to generate the final diffusion image. Fig. 1 shows the self-calibrated eGRAPPA reconstruction pipeline using 3-shot as an
example (a), a simple demonstration of GRAPPA and eGRAPPA (b) and a simple
comparison of navigated and navigator-free sequence (c).
Experiments Human liver DWI scans were performed on a Philips 3.0T
MRI scanner (Philips Healthcare, Best, The Netherlands) using a 16-channel
abdominal coil. Data were acquired from 2 healthy volunteers under IRB approval
from our institution. A navigated ms-EPI sequence was scanned for comparing different reconstruction results with and without using the acquired
navigators. The data were acquired using free-breathing with respiratory
trigger, acquisition voxel size = 2 × 2 × 6 mm3,
4 shots with 22 echoes per shot, partial Fourier factor = 0.7, TE = 41 ms, scan
time = ~3 min, 3 orthogonal diffusion directions with
b = 500 s/mm2, NSA = 4. For comparison, ss-EPI DWI (acquisition
voxel size = 3 × 3 × 6 mm3) with GRAPPA = 2 was also scanned for references.
Proposed self-calibrated eGRAPPA method was compared with navigator-calibrated eGRAPPA,
image-domain self-calibrated MUSE7 and conventional
GRAPPA-average reconstruction8. For the k-space interpolation kernel
size, 3×3 was used in the first GRAPPA step and 3×5 in the second
eGRAPPA step.
Results and Discussion
Fig. 2
shows the isotropic liver DWI using ss-EPI as a reference (a), ms-EPI without
correction (b), with conventional GRAPPA correction (c), with proposed self-calibrated
eGRAPPA correction (d), with navigator-calibrated eGRAPPA correction (e) and
with MUSE correction (f). The phase errors cause severe ghost artifacts in
ms-EPI if no correction is performed (b). The proposed correction method (d)
can correct these ghost artifacts, and reduced noise level can be visually seen
compared with conventional GRAPPA-average correction (c). Proposed
self-calibrated eGRAPPA (d) and navigator-calibrated eGRAPPA (e) provide
similar image quality in the shown slice. Image-domain MUSE result (f) also
shows effective correction except for some residual artifacts (yellow arrow
heads). This may be caused by the insensitivity to motion of eGRAPPA inherited from
GRAPPA8, compared with SENSE-based method.
We
further compared self-calibrated and navigator-calibrated eGRAPPA and chose three
slices shown in Fig. 3. In these cases, although navigator-calibrated method
can correct most of the ghost artifacts, proposed self-calibrated method shows
better correction with fewer residual artifacts (yellow arrow heads). The reason can be that the self-calibrated strategy is not sensitive to the potential mismatch
between image and navigator echoes due to different distortion levels,
resolutions1,2,5 (e.g. Fig. 1c),
motion states or signal attenuation (T2 decay, non-CPMG).
The
navigator-free ms-EPI sequence uses single-echo spin-echo acquisition, instead
of navigated two-echo spin-echo sequence, in order to improve the scan efficiency.
In the meantime, the image quality is not affected much (Fig.2 d,e), and sometimes
even shows better correction (Fig. 3). However, like other two-step
self-calibrated methods (MUSE, etc.), the number of shot to cover the full
k-space is still limited in the first calibration step (e.g. no more than 6-shot
using 8-channel coils), which is not the limitation for methods with navigator
acquisitions.
Conclusion
The
proposed self-calibrated eGRAPPA method can correct motion induced ghost
artifacts in multi-shot diffusion imaging, which is efficient without the need
for navigator acquisitions in sequences.
Acknowledgements
This work was
supported by National Natural Science Foundation of China (61271132, 61571258)
and Beijing Natural Science Foundation (7142091).References
[1] Ma X
et al. ISMRM 2015;p2799.
[2] Guo H at
al. ISMRM Workshop on SMS Imaging 2015.
[3] Liu W
et al. Magn Reson Med. 2015;epub.
[4]
Griswold M a et al. Magn Reson Med. 2002;47.
[5] Jeong
H-K et al. Magn Reson Med. 2013;69.
[6] Skare
S et al. ISMRM. 2009;p1409.
[7] Chen
N-K et al. Neuroimage. 2013;72.
[8] Skare S et al. Magn
Reson Med. 2007;57.