Diffusional Kurtosis Imaging of Kidneys in Children with Chronic Kidney Disease: Initial Experience
Yang Wen1, Yun Peng1, Dan Dan Zheng2, Zhi Chen3, Guang Heng Yin1, Yan Qiu Lv1, Chen Xu1, and Yang Fan2

1Department of Radiology, Beijing Children’s Hospital Affiliated to Capital Medical University, Beijing, China, People's Republic of, 2GE Healthcare, MR Research China, Beijing, China, People's Republic of, 3Department of Nephrology, Beijing Children’s Hospital Affiliated to Capital Medical University, Beijing, China, People's Republic of

Synopsis

To evaluate the feasibility of DKI in assessment of renal functions in children with chronic kidney disease (CKD). Materials and Methods: This study was IRB approved and informed consent was obtained. Fifteen pediatric patients with CKD and nine children without renal diseases underwent DKI of kidneys. Maps of fractional anisotropy (FA), mean diffusivity (MD), mean kurtosis (MK), radial kurtosis (K) and axial kurtosis (K//) were produced. Results: There is a significant difference of kurtosis metrics and FA of renal medulla compared to those of renal cortex in both the control group and CKD group. FA, MD, K and MK values of both the cortex and medulla of kidney have significant differences between patients with CKD and control group. Conclusion: DKI could be a useful tool in the evaluation of renal function in children with CKD.

Purpose

Diffusion-weighted imaging (DWI) and diffusion tensor imaging (DTI) have demonstrated clinical potential to evaluate renal functions in patients with chronic kidney disease (CKD) [1, 2]. However, inconsistent assessments of renal functions were obtained using DWI/DTI in patients with CKD [1-3]. Based on non-Gaussian properties of water diffusion, diffusional kurtosis imaging (DKI) can offer additional information about microstructural complexity of biological tissues [4]. Recently, due to respiratory triggering technique, the feasibility of DKI in human kidneys has been confirmed [4, 5]. The purpose of this study is to prospectively evaluate the feasibility of DKI in assessment of renal functions in children with CKD.

Materials and Methods

This study was IRB approved and informed consent was obtained. Fifteen pediatric patients with CKD (aged from 3 years to 10 years) and nine children without renal diseases (age ranging from 3 to 7 years) as a control group were enrolled in this study. All subjects underwent transverse, respiratory-triggered, single-shot spin-echo echo-planar DKI of kidneys. DKI with 15 directions and 3 b-values (0, 500, 1000 s/mm2) was performed on a 3.0T MR scanner (GE DISCOVERY MR 750, USA) after scans of routine anatomical images. Maps of fractional anisotropy (FA), mean diffusivity (MD), mean kurtosis (MK), radial kurtosis (K) and axial kurtosis (K//) were produced. For each subject, three representative axial slices in the upper pole, mid-zone and lower pole were selected in the left and right kidneys. On each selected slice, three regions of interest were drawn on the renal cortex and another three on the medulla as shown in Fig.1A. Statistical comparisons were conducted using t-test and analysis of variance.

Results

No statistically significant difference was observed between the left and right kidneys for all metrics in both the control group and CKD group. Kurtosis metrics (MK, K//, K) obtained in the renal medulla were significantly higher than those of cortex for both groups. FA of the medulla was significant higher than that of the cortex in both the normal and affected kidneys (p < 0.001). MD (mm2/ms) was lower in the medulla than in the cortex only in control group (p < 0.01), and there is no statistically significant difference in CKD group (p=0.475). Regardless of whether eGFR (estimated glomerular filtration rate according to the serum creatinine level) was reduced, FA of both the cortex and the medulla was significantly lower in patients with CKD than in control group (p < 0.01), MD of both the cortex and the medulla was significantly higher in patients with CKD than in controls (p < 0.05), and K and MK of both the cortex and the medulla were lower in patients with CKD than in controls (p < 0.05). No statistically significant differences of K// were observed between two groups of subjects. A direct correlation between DKI parameters and the eGFR was not found.

Discussion and Conclusion

This study demonstrates that there is a significant difference of kurtosis metrics and FA of renal medulla compared to those of renal cortex in both the control group and CKD group. FA, MD, K and MK values of both the cortex and medulla of kidney have significant differences between patients with CKD and control group. The preliminary results suggest that DKI could be a useful tool in the evaluation of renal function in children with CKD.

Acknowledgements

No acknowledgement found.

References

1.Xu X et al. Diffusion-weighted MR imaging of kidneys in patients with chronic kidney disease: initial study. Eur Radiol. 2010; 20(4):978-83.

2. Liu Z et al. Chronic kidney disease: pathological and functional assessment with diffusion tensor imaging at 3T MR. Eur Radiol. 2015;25(3):652-60.

3. Toya R et al. Correlation between estimated glomerular filtration rate (eGFR) and apparent diffusion coefficient (ADC) values of the kidneys. Magn Reson Med Sci. 2010;9(2):59-64.

4. Pentang G et al. Diffusion kurtosis imaging of the human kidney: a feasibility study. Magn Reson Imaging. 2014;32(5):413-20.

5. Huang Y et al. MRI quantification of non-Gaussian water diffusion in normal human kidney: a diffusional kurtosis imaging study. NMR Biomed. 2015;28(2):154-61.

Figures

Fig.1. (A~ C) are from a five years old girl in control group. (A) Representative locations of ROIs for the cortex and medulla at the mid-zone of the right kidney on the b = 0 mm2/s image. (B) and (C) are maps of MK and K, respectively.

Fig.2. (A,B) are maps of MK and K from a ten years old boy with CKD, in turn. K and MK of both the cortex and the medulla significantly decrease in the patient with CKD than in the control shown in Fig.1.



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
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