Qiang Liu1,2,3, Yingjie Mei1,2,3, Quan Tao1,2,3, Qiqi Lu1,2,3, Xinyuan Zhang1,2,3, and Yanqiu Feng1,2,3
1School of Biomedical Engineering, Southern Medical University, Guangzhou, China, 2Guangdong Provincial Key Laboratory of Medical Image Processing & Guangdong Province Engineering Laboratory for Medical Imaging and Diagnostic Technology, Southern Medical University, Guangzhou, China, 3Guangdong-Hong Kong-Macao Greater Bay Area Center for Brain Science and Brain-Inspired Intelligence & Key Laboratory of Mental Health of the Ministry of Education, Southern Medical University, Guangzhou, China
Synopsis
We introduced blip-up/down acquisition (BUDA) strategy
for interleaved 2-shot EPI to achieve motion robust, distortion-free rat renal diffusion-weighted
imaging (DWI). Dual-polarity GRAPPA (DPG) method was implemented to correct
Nyquist ghost artifact while simultaneously reconstructing the undersampled 2-shot
data, then the field map was estimated from the opposing-distorted images. The
field map was incorporated into a joint reconstruction with a structure
low-rank constraint across the two shots to eliminate distortion and phase
inconsistencies. DPG-BUDA permits high anatomical integrity while holding high
scan efficiency for renal DWI in small rodents, it has the potential to benefit
the characterization of the renal microstructure.
Introduction
As a non-invasive magnetic resonance imaging (MRI)
technique, renal diffusion-weighted imaging (DWI) probes the microstructure
integrity and function of renal tissues, which is getting increasingly popular
in both pre-clinical and clinical studies1.
At an ultra-high magnetic field, single-shot echo-planar imaging (ss-EPI) based
renal DWI suffers from severe image distortion which can be mitigated by
multi-shot EPI (ms-EPI) variants. Further, to eliminate the distortion, the
field map related to B0 inhomogeneity and eddy current in DWI can be derived
from blip-up/down acquisition (BUDA) for interleaved 2-shot EPI using FSL toolbox
TOPUP2,3,
and then can be incorporated into the reconstruction framework. Recently, the
propose of BUDA and joint parallel-imaging reconstruction with a structured low-rank
constraint framework enables distortion-free and navigator-free high-resolution
DWI in the human brain4,5.
In this work, we extended this approach to renal DWI in small rodents to
examine the feasibility of BUDA to enhance kidney DWI. In current practice, instead
of using SENSE + local phase correction (LPC) method, we implemented the
dual-polarity GRAPPA (DPG) method to correct the Nyquist ghost while simultaneously reconstructing the undersampled blip-up/down
data, which has shown priority
to the LPC method6, and we termed this acquisition and reconstruction framework
DPG-BUDA.Methods
Figure 1 presents the pipeline of the DPG method: two
groups of interleaved 2-shot EPI were acquired (with opposing readout gradients,
termed RO+ and RO-), the RO+ and RO- readout lines were combined separately, and
then temporally encoded ghost-free auto-calibration signals (ACS) were obtained
through GESTE7
to train DPG kernels, the undersampled data were reconstructed and corrected through
this kernels.
Figure 2 presents the framework of the DPG-BUDA
acquisition and reconstructed method. Interleaved 2-shot EPI with reversed
phase-encoding gradient polarities sampled the k-space. The opposite-distortion
images were reconstructed by the DPG method, and by using FSL TOPUP, the
field map which contains B0 inhomogeneity and eddy current effects was
calculated. The field map was then incorporated into a joint reconstruction
with a structure low-rank constraint across 2-shot:
$$min\sum_{t=1}^{N_{s}}||F_{t}E_{t}Cx_{t}-d_{t}||_2^2+\lambda||H(x)||_{*}$$
where Ft is the undersampled Fourier operator
in tth shot; Et is the calculated field map; C are the coil-sensitivities; xt is the distortion-free image and dt are the k-space data for shot
t. The constraint ||H(x)||* enforces Hankel low-rank prior on the k-space
data xt.
This
study was approved by the local Institutional Animal Care and Use Committee.
All MRI experiments were carried out on a 7.0 T small animal MR scanner
(PharmaScan; Bruker BioSpin, Ettlingen, Germany), image reconstructions were
performed in Matlab (MathWorks, Natick, MA).Results
Figure 3 presents representative images from DPG-BUDA
method, with both b-value=0 and b-value=500 s/mm2. Both the inter-
and intra-structures of renal tissues are clearly depicted by DPG-BUDA. In the
left column, the kidney contours were manually segmented for T2W-RARE image,
and then were superimposed to the DPG-BUDA images (the medium and the right
column of figure 3). Compared with the reference distortion-free T2W-RARE
image, the DPG-BUDA yielded high anatomical fidelity.
The quantitative mean diffusivity (MD) and fractional anisotropy (FA) maps obtained from DPG-BUDA are displayed in Figure 4. From
the FA map, a high degree of diffusion anisotropy in the inner stripe of the
outer medulla can be observed. Discussion and Conclusions
This work demonstrates that renal DWI with high
anatomical fidelity can be achieved by the introduced DPG-BUDA acquisition and
reconstruction framework. At an ultra-high magnetic field, the spatial resolution
of renal DWI is often limited by severe image distortion caused by B0
inhomogeneity and eddy current effects. With a highly efficient interleaved
blip-up/down acquisition strategy, the field map can be derived and incorporated
into the reconstruction framework to eliminate the distortion. DPG-BUDA method provides high anatomical integrity
and high scan efficiency and may has the potential to benefit the study of TE-dependent diffusion imaging to quantify volume fractions of Intra-/inter-tubular
water compartments in renal tissues8,9.Acknowledgements
The
authors wish to thank Dr. Congyu Liao of Stanford University for generously
sharing his BUDA code and Dr. W. Scott Hoge of Harvard Medical School for
the inspiration about using DPG reconstruction method and discussion on how to implement it on the Bruker
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