Liyun Zheng1,2, Chun Yang3, Ruofan Sheng3, Yongming Dai2, and Mengsu Zeng1,3
1Shanghai Institute of Medical Imaging, Shanghai, China, 2United Imaging Healthcare, Shanghai, China, 3Department of Radiology, Zhongshan Hospital, Fudan University, Shanghai, China
Synopsis
Compared to clinical field strengths, MRI at ultra-high magnetic fields allows higher SNR. However, imaging at 7T remains challenging, especially in renal MRI. This study investigated the feasibility of renal MRI at 5T, with a brand new 5T MR scanner. Compared to 3T examination, 5T renal MRI demonstrated higher SNR and improved corticomedullar discrimination with diagnostic image quality. Functional imaging, including DWI and T2* mapping, was also feasible at 5T. Therefore, in vivo 5T renal MRI may better elucidate the renal diseases with both anatomical and functional imaging, compared to conventional clinical MRI scanners.
Introduction
Generally,
higher magnetic field allows higher signal-to-noise (SNR) ratio, and gives more
space for spatial resolution. On the other hand, the changed relaxation time,
i.e., T1 and T2, and other physical effects such as inhomogeneity
of the radiofrequency field and specific absorption rate (SAR) constraints due
to higher field make a challenge for image quality [1]. Renal
magnetic resonance imaging (MRI) is a significant part of clinical routine. Prior
study demonstrated the potential and drawbacks of 7T renal MRI [2]. In this
study, we aimed to investigate the performance renal MRI at 5T, and compare it with
3T.Methods
Fifteen
healthy volunteers with no known renal diseases were included in this study. This
study was approved by institutional review board and written signed consents
were obtained from all participants. All the participants were examined on a 3T
MR scanner (uMR 790, United Imaging Healthcare, Shanghai, China) and a 5T MR scanner
(uMR Jupiter, United Imaging Healthcare, Shanghai, China) by using optimal coil
setups for both field strengths, respectively. At 5T, a custom-built 24 channel
body transmit/receive RF coil was used, and B1+ shimming was used for B1+
optimization. The MRI sequences included coronal T1-weightd 3D volume-interpolated
breath-hold gradient-echo (GRE) sequence (QUICK 3D), axial T2-weighted fast
spin-echo (FSE) with fat saturation and respiratory trigger, and diffusion
weighted imaging (DWI). T2* mapping was performed based on multi-echo GRE
sequence. The detailed MR protocols were listed in table 1.
Qualitative
and quantitative analyses were performed in consensus by two experienced
radiologists. The image quality for each sequence type was evaluated by using a
three-point scale (score 1 = poor quality, score 2 = moderate [diagnostic]
quality, score 3 = good quality). The evaluation criteria were based on: 1) the
cortico-medullary differentiation and 2) the delineation of adrenal glands,
proximal ureter, renal arteries, and renal veins. Considering the chemical
shift, B1 inhomogeneity, susceptibility, motion artifacts and the overall image
impairment, the presence of artifacts was assessed by using a three-point scale
(score 1 = strong impairment, score 2 = moderate impairment, score 3 = no artifact
present or insignificant). For the quantitative analysis, SNR (cortex) = Signal
(cortex)/noise, SNR (medulla) = Signal (medulla)/noise, and CNR =
[Signal(cortex)-Signal(medulla)]/noise were measured for images of all the
sequences. The noise was defined as the standard deviation of signal intensity
within air outside of the body.
For
functional imaging, mean apparent diffusion coefficient (ADC) and T2*
relaxation time were calculated from cortex and medulla for each subject,
respectively.
Score values
of image quality and presence of artifacts for each sequence, and the mean ADC
and T2* values were compared between 3T and 5T using Wilcoxon’s Rank Test. The
Wilcoxon signed rank-sum test was also used to compare the individual cortical
and medullary T2* and ADC of all the subjects. The Bonferroni correction was
used to adapt the multiple tests. P value < 0.05 was considered
statistically significant.Results
All 5T
examinations were performed successfully and were well tolerated by the
subjects without any side effects. Representative anatomical images and
functional maps are shown in Figure 1-4.
For all the
sequences, the image quality of 5T images was significantly higher than 3T
images (P < 0.05) while there was no significant difference between the
present of artifacts. Compared to 3T MRI, the SNR of cortex at 5T MRI achieved
1.5-fold in T1-weighted sequence, 1.2-fold in T2-weighted sequence, 1.5-fold in
DWI, and 1.2-fold in T2* mapping. The SNR of medulla at 5T MRI achieved
1.5-fold in T1-weighted sequence, 1.2-fold in T2-weighted sequence, 1.6-fold in
DWI, and 1.2-fold in T2* mapping. Besides, the CNR of cortex/medulla at 5T MRI
provided approximately 1.5-, 1.4-, 1.8-, and 1.5-fold increase from 3T to 5T in
T1-weigthed, T2-weighted, DWI, and T2* mapping sequences, respectively.
For
the functional maps, ADC of the cortex was significantly higher than that of the
medulla at both 3T and 5T (P < 0.05). There were no statistically
significant differences for the ADCs between 3T and 5T. Further, T2* value of
the cortex was also significantly higher than that of the medulla at both 3T and
5T (P < 0.05). Compared to 3T, renal MRI at 5T resulted in significantly
shorter T2* values in both cortex (66.14 ms in 3T and 44.62 ms in 5T) and
medulla (30.39 ms in 3T and 16.67 ms in 5T).Discussion/Conclusion
This first
attempt at dedicated 5T renal imaging revealed the diagnostic potential. At 5T,
SNR of cortex and medulla and CNR of cortex/medulla were significantly higher
than that at 3T, leading to improved corticomedullary discrimination. The improved SNR
and CNR has been shown to be beneficial in various applications of diagnostic
high-field MRI [3, 4]. For the
functional maps, renal DWI at 5T held a similar ADC range with that at 3T, which is expected as ADC is not affected by the field strength. In accordance with
previous studies [5, 6], T2*
relaxation times decreased with the increase of magnetic field strength. Acknowledgements
No acknowledgement found.References
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