Yizhe Zhang1,2,3, Quan Tao2,3,4, Zelong Chen5, Zhigang Wu6, Wenyan Zhang1,2,3, Qianqian Zhang1,2,3, Kan Deng7, Peng Wu8, Yikai Xu5, and Yanqiu Feng1,2,3,4
1School of Biomedical Engineering, Southern Medical University, Guangzhou, China, 2Guangdong Provincial Key Laboratory of Medical Image Processing, Southern Medical University, Guangzhou, China, 3Guangdong Provincial Engineering Laboratory for Medical Imaging and Diagnostic Technology, Southern Medical University, Guangzhou, China, 4Department of Rehabilitation, Zhujiang Hospital, Southern Medical University, Guangzhou, China, 5Medical Imaging Center, Nanfang Hospital, Southern Medical University, Guangzhou, China, 6Philips Healthcare, Shenzhen, China, 7Philips Healthcare, Guangzhou, China, 8Philips Healthcare, Shanghai, China
Synopsis
Keywords: Arterial Spin Labelling, Arterial spin labelling
Motivation: Renal imaging using echo planar imaging (EPI) readout may be sensitive to field inhomogeneities and induced ghost artifact. Besides, single inversion time is not enough for renal blood flow (RBF) quantification. Investigation of more stable clinical arterial spin label (ASL) imaging methods is required.
Goal(s): We aimed to design a stable clinical ASL sequence to quantify RBF accurately.
Approach: Multiple inversion time (TIs) readout by turbo spin echo (TSE) was processed, and the repeatability of quantification was evaluated in volunteers (n=7).
Results: Multiple TIs combined with TSE readout of FAIR-ASL provided more accurate RBF measurement and highly repeatability compare with pcASL-EPI.
Impact: Multi-PLDs readout by TSE may provide a stable
clinical ASL-FAIR sequences to accurately quantify RBF.
Introduction
Functional imaging of blood flow, such as ASL[1],
is sensitive to renal injury or disease[2]. Current clinical single–PLD ASL-EPI
sequences are unstable and poorly repeatable and difficult to quantify renal
blood flow. In this abstract, we designed renal multi-TI-ASL sequence readout
by TSE and verified its stability and repetition in clinical measurement of RBF.Method
Sequence
design:
Figure 1 shows the sequence design in this study. The sequence consists of two components: the label
module and the readout module. The label pulse consisted by an adiabatic flip pulse, which reduces the
effect of B1 inhomogeneities.
MRI:
This experiment was approved by local institutional
Review Board. MRI data were acquired in seven healthy volunteers (n=7) under
breath hold on a Philips 3.0T scanner(Ingenia , Philips Healthcare, Best, The Netherlands)equipped with 32 channels torso coil. MRI examination
was performed twice with one week interval to test the feasibility and
repeatability. The ASL-FAIR sequence used the following acquisition parameters:
FOV = 384 x 384 mm2, matrix= 256x256, resolution = 1.5x1.5 mm2,
slice thickness = 5 mm, label thickness = 15 mm, control thickness = 500 mm, TR/TE
= 4500/5.1 ms, single-shot TSE. In addition, single slice imaging was conducted
for signal sampling of 9TIs (300,600,900,1200,1500,1800,2100,2400 and 3000ms).
Data
Analysis:
The image processing and analyses were performed on
MATLAB R2022b(The MathWorks,Natick,MA). The images were registered by principal
component analysis (PCA) using Elastix[3], and de-noised by Non-Local Means. Then,
the images were fitted by inversion recovery T1 model. The
perfusion measurements of the kidney were calculated by the classic Buxton
model [4]. Subsequently, the renal cortex region of interests (ROIs) were
determined manual on the T1mapping image and applied to all registered
datasets.
Statistical
Analysis:
The RBF value was expressed as mean ± standard
deviation (SD). We used Bland-Altman to test the reproducibility, with
confidence intervals set at 5%.Results
The cortical RBF of healthy subjects is 435.30 ±
20.895 mL/100 g/min for the left renal cortex and 432.08 ± 20.934 mL/100 g/min
for the right kidney. Figure 2 shows the perfusion-weighted images and RBF maps
imaged by single-PLD-EPI and multi-TI-TSE, respectively. The multi-TI-TSE
approach produces a renal RBF image with a well-defined renal structure and
distinct borders at two scanning, however, the perfusion-weighted images
exhibited blurred boundaries and poor image quality at re-scan. The
Bland-Altman analysis showed that the all volunteers’ RBF measured by
multi-TI-TSE ASL are all within the 95% confidence interval (Figure 3), which
indicates the high stability and repeatability of our sequence.Discussion
Renal blood flow (RBF) is a
potential indicator for kidney disease detection. This study provided a stable
and highly repeatable measurement approach, which is beneficial for clinical
applications.
However, there
are some limitations to this study. The first is the problem of motion, which
requires an accurate registration method. The second is that the model utilizes
a single-compartment model, which only considers the inflow and outflow of
blood flow, with no internal transformations. More investigations on model
simulation and motion correction are needed.Conclusion
Our work validates the effectivity of multiple
TI/PLD FAIR for RBF imaging. This sequence has been demonstrated that with
great stability and repeatability in healthy volunteers.Acknowledgements
This study was supported by National Natural Science Foundation of China (U21A6005), Key-Area Research and Development Program of Guangdong Province (2018B030340001, 2018B030333001).References
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