Anshuman Panda1, Justin Yu1, Michael Schwartz1, Helen Looker2, Robert Nelson2, Kelly Smith1, Aidan McGirr1, Sophia Fasani1, Sukhdeep Singh1, Kristina Flicek1, and Alvin Silva1
1Mayo Clinic Arizona, Scottsdale, AZ, United States, 2National Institutes of Health, Bethesda, MD, United States
Synopsis
The purpose of this pilot study is to determine
technical feasibility and correlate MR
Elastography (MRE) and Proton Density Fat Fraction (PDFF) with gold standard
assessments of glomerular function and histopathology markers.
Introduction
An estimated 30 million
American adults have chronic kidney disease (CKD), with many more at risk. As early detection can help prevent
progression to kidney failure, and current relevant clinical assessments are
relatively deficient and/or have attendant risks/complications, there is need
for identification of improved noninvasive biomarkers for end-organ
damage. The purpose of this pilot study
is to determine technical feasibility and correlate advanced MR imaging
techniques MR Elastography (MRE) and Proton Density Fat Fraction (PDFF) with
gold standard assessments of glomerular function and histopathology markers.Method
Eleven patients were scanned with a 1.5T MRI (General
Electric, Waukesha, Wisconsin) with 8-channel body coil. Axial and coronal MRE
and PDFF scans were performed. For PDFF,
whole kidney acquisitions were be performed using a complex-based, six-echo 3D chemical
shift-encoded method (ref 1, 2). Kidney MRE was performed in the same session with a
modified 3D EPI phase-contrast sequence which were then processed with an inversion algorithm to generate a quantitative image
of shear stiffness (ref 3, 4, 5). The MRE scans were performed in axial and coronal-oblique planes. The
MRE and PDFF measurements were performed by manually by drawing ROI on left and
right kidney medulla. The biopsy samples were analyzed on a paraffin media. The following histopathology
markers were evaluated for correlation with MRE and PDFF: GBM (glomerular
basement membrane width), P_FPW (foot
process width in peripheral glomerular basement membrane), INTACT (percent of
intact foot processes on both the peripheral and mesangial glomerular basement
membrane), P_FEN (percent of endothelial fenestration falling on the peripheral
glomerular basement membrane), and VVINT
(cortical interstitial fractional volume).Results
Biopsy
glomerulosclerosis percent varied from 0% to patient with normal kidney to 45%
for patients with low GFR. The PDFF measurements ranged from 0-3% and
elasticity measurements ranged from 2.8 kPa to 5.4 kPa. Discussion
Patients with biopsy glomerulosclerosis
percent greater than 0% showed higher kidney stiffness measuring greater than 4.0
kPa on MRE. No significant correlation was observed between biopsy glomerulosclerosis
percent and PDFF. Further no correlation was observed between MRE and PDFF
measurements. Conclusion
To our knowledge this is the first study correlating MRE/PDFF and several key histopathology markers (GBM, P_FPW, INTACT, P_FEN, and VVINT) in patients with diabetic kidney disease. MR Elastography of kidney could be a viable imaging biomarker for correlating MR measurements with histopathology.Acknowledgements
No acknowledgement found.References
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