The accuracy of MRI based glomerular filtration rate (GFR) measurements using the standard Cartesian VIBE DCE-MRI is limited by motion and temporal resolution. Instead, we use motion-robust high temporal resolution radial VIBE for DCE-MRI for accurate estimation of GFR. We optimize its temporal resolution and compressed sensing reconstruction temporal regularization parameters to obtain an accurate arterial input function peak while reconstructing good quality images. We also developed a fully automated segmentation and tracer kinetic model-fitting pipeline to compute MRI-GFR. We assessed the accuracy of proposed technique to measure GFR by comparing MRI-GFR to GFR from 99mTcDTPA nuclear medicine study (NMGFR).
Introduction
Dynamic Contrast Enhanced (DCE) MRI can be used to measure renal function, i.e. glomerular filtration rate (GFR). DCE-MRI using standard Cartesian-VIBE has several limitations including 1) respiratory motion in free-breathing scans which reduces image quality and significantly lowers the accuracy of MRI-GFR estimates; 2) insufficient temporal resolution, which results in a failure to measure the arterial input function (AIF) peak needed for accurate estimates of GFR because AIF changes rapidly after contrast injection; 3) a lack of specialized software for fully automated segmentation of kidney parenchyma, aorta and for performing tracer kinetic model fitting for robust GFR estimation. In this work, we use a motion-robust high spatiotemporal resolution DCE-MRI using dynamic radial VIBE (DRV) sequence, compressed-sensing offline-reconstruction using temporal regularization and a fully automated processing pipeline to measure MRI-GFR. We optimize the parameters (temporal resolution and regularization) to achieve accurate GFR estimation and good image quality at the same time. We then assess the accuracy of measuring GFR with this technique by comparison of MRI-GFR to gold standard GFR from 99mTcDTPA nuclear medicine study (NM-GFR).Children, between 0-20 years, undergoing both a clinically indicated contrast-enhanced MRI, and a nuclear medicine GFR study within 2 weeks of each other, underwent an IRB approved additional 6-minute DCE-MRI kidney scan using the motion-robust high spatiotemporal resolution dynamic radial VIBE sequence (3T Siemens Skyra/Trio, radial “stack-of-stars” 3D FLASH prototype Siemens sequence with TR/TE/FA 3.56/1.39ms/12o, 32 coronal slices, voxel size=1.25x1.25x3mm, 1326 radial spokes in 6 mins, golden angle radial ordering). Contrast was injected using bolus injection (0.2ml/s). 4D dynamic image series were reconstructed offline using compressed-sensing reconstruction1 (using the Matlab code provided by NYU that we modified) to improve image quality, effectively reducing the streaking artifacts. We analyzed the effect of regularization parameter and temporal resolution on the AIF peak and image quality and chose the optimal parameters that satisfied both criteria.
Images were automatically post-processed using in-house developed software. Post-processing steps included segmentation of kidney parenchyma2 and aorta using fully convolutional neural network (F-CNN) techniques. Figure 2 shows the cascaded detection and segmentation steps for segmentation of left and right kidneys using a F-CNN2. The steps included: 1) detection of left and right kidneys given a time series of 3D volumes (4D data); 2) generating a safer enlarged bounding box and 3) segmentation of each kidney. Before detection, we applied PCA to reduce the time dimension and downsampling in spatial dimensions for memory efficiency. After segmentation, we converted the tissue enhancement curves of aorta and kidneys to concentration curves, selected aorta voxels with largest peak and fitted Sourbron et al.’s3 separable two-compartment tracer kinetic model to compute the filtration rate parameter (FT). MRI-GFR is calculated by multiplying FT with renal parenchyma volume. The MRI-GFR results were compared to the GFR measured by 99mTcDTPA nuclear medicine study (NMGFR).