Pan Wang1, Min Li1, Xiangnan Li1, Jiyang Zhang1, Xin Zheng2, Chen Zhang3, Stemmer Alto4, and Tao Jiang1
1radiology department, Beijing Chao-Yang Hospital, Beijing, China, 2Urinary Surgery, Beijing Chao-Yang Hospital, Beijing, China, 3MR Scientific Marketing, Siemens Healthcare, Beijing, China, 4] MR Application Development, Siemens Healthcare, Erlangen, Germany
Synopsis
Kidney transplantation is currently considered as the preferred treatment
for end-stage renal disease, this study aims to explore the performance of BOLD-fMRI
and IVIM of renal transplants kidney patients with CKD. The results showed the D
value in renal cortical could well identify and distinguish normal kidney and diseased
kidney. The R2* value could indirectly reflect deoxyhemoglobin to assess the degree
of renal function impairment. BOLD-fMRI and IVIM can provide a more accurate and
comprehensive understanding of the functional information of the chronic kidney
metabolism.
Introduction
Kidney transplantation is currently considered as
the preferred treatment for End-Stage Renal Disease (ESRD). With the
improvement and maturity of renal transplantation surgical technology[1], especially the application of new immunosuppressants, the survival rate
of early transplantation patients has increased significantly [2]. However, most kidney transplant patients still develop chronic kidney
disease (CKD), and even face the risk of renal failure due to postoperative complications
and other related factors[3,4],In the past, diffusion-weighted magnetic resonance
imaging (DWI) and apparent diffusion coefficient (ADC) were used to access the
transplanted kidneys, and the long-term outcome after Kidney transplantation
has not been improved[5]. The progression of CKD is a process of renal
interstitial fibrosis caused by pathophysiological processes such as ischemia
and hypoxia, leading to a decrease in local blood flow[6].Therefore, this study aims to explore the
performance of blood oxygen level dependent functional MRI (BOLD-fMRI) and intravoxel
incoherent motion (IVIM) MRI of renal transplants kidney patients with CKD, and
provide a basis for the application of fMRI in the evaluation of renal
transplant function.Method
104 patients of stable disease after renal transplantation
more than 3 months were retrospectively considered as the case group. The case
group was divided into 3 groups according to
eGFR: eGFR ≥ 60 ml / (min · 1.73 m2) for mild CKD group 1, 11 patients;
30 ml / (min · 1.73 m2) ≤ EGFR < 60 ml / (min · 1.73 m2) for moderate CKD group 2,
61patients; eGFR < 30ml / (min · 1.73 m2) for severe CKD group 3, 32 patients. 36
healthy volunteers were selected as control named 0 group,as shown in Table1. Clinical
Routine MRI, BOLD-fMRI and IVIM MRI were performed in both cases and controls
to measure the cortical and medullary, all data were collected on a 3T MR
scanner (MAGNETOM Prisma, Siemens Healthcare, Erlangen, Germany) through an
18-element abdominal coil array. An integrated prototypical slice-by-slice shimming
(iShim) technique was used which dynamically updatesthe frequency and the
linear shim terms prior to the acquisition of each slice during the imaging phase.
The parameters are as follows: TR/TE =3700/59ms, slice thickness=4mm, FOV=245×350mm2,
Bandwidth = 2195 Hz/px, b-values = 0, 50, 100, 150, 200, 400, 800, 1200, 2000,
3000 s/mm2. BOLD were acquired using a multi-echo GRE
protocol with the following parameters: TR=440ms, TE=2.46ms, 4.95ms, 7.39ms,
9.88ms, slice thickness=4 mm, in-plane resolution= 1.1×1.1 mm2, FOV=250×250mm2, flip angle= 25 deg,
slices= 20, distance factor=10%.
R2* values, D values, D* values, and fp values
of kidneys in the control and case groups were acquired, as shown in Fig 1 and
Fig 2. The analysis of these parameters between cortex and medulla in the control
and case groups were performed by using SPSS 22.0 statistical software, t test,
the One-Way ANOVA and LSD method.Result
Table 2 and 3,figure 1 and 2 show analysis results of R2* values,
D values, D* values, and fp values of control and case groups.
R2* values of renal medulla and D values of renal cortex between each group are
statistically significant (all p < 0.05). D* values and fp values of
renal cortex and medulla in control group are higher than group 2 and 3 (all p
< 0.05). For case groups, R2* values of renal cortex、D values of renal medulla、D* values and fp values of renal cortex
and medulla are also analyzed, there was no statistically significant difference
(all p>0.05).Discussion and Conclusions
In this study,R2* value and
D value can well distinguish the normal kidney tissue from the kidney tissue
with functional impairment. BOLD-fMRI and IVIM can provide a more accurate and comprehensive
understanding of the functional information of the chronic kidney metabolism, which
is beneficial to selection treatment drug,and provides an important reference value for the
diagnosis, staging, treatment and prognosis of CKD in
transplanted kidneys.Acknowledgements
We sincerely thank the participants in this study.References
[1] Wolfe R A, Ashby V B, Milford E L, et al.
Comparison of mortality in all patients on dialysis, patients on dialysis
awaiting transplantation, and recipients of a first cadaveric transplant[J]. N
Engl J Med, 1999, 341(23): 1725-30.
[2] Haririan A. Current status of the
evaluation and management of antibody-mediated rejection in kidney
transplantation[J]. Curr Opin Nephrol Hypertens, 2015, 24(6): 576-81.
[3] Meier-Kriesche H U, Schold J D, Srinivas T
R, et al. Lack of improvement in renal allograft survival despite a marked
decrease in acute rejection rates over the most recent era[J]. Am J Transplant,
2004, 4(3): 378-83.
[4] Meier-Kriesche H U, Schold J D, Kaplan B.
Long-term renal allograft survival: have we made significant progress or is it
time to rethink our analytic and therapeutic strategies?[J]. Am J Transplant,
2004, 4(8): 1289-95.
[5] Juillard L, Lerman L O, Kruger D G, et al.
Blood oxygen level|[ndash]|dependent measurement of acute intra-renal ischemia[J].
Kidney International, 2004, 65(3): 944-950.
[6] Eddy A A. Molecular basis of renal
fibrosis[J]. Pediatric Nephrology, 2000, 15(3-4): 290-301