Emma Doran1, Stephen Bawden1, Christopher Mirfin1, Paul Glover1, Richard Bowtell1, Penny A. Gowland1, and Susan Francis1
1Sir Peter Mansfield Imaging Centre, University of Nottingham, Nottingham, United Kingdom
Synopsis
Chronic Kidney Disease (CKD) is thought to be due to small artery disease
at the cortico-medullary border, however these vessels are too small to be
imaged at conventional field strengths. Here, we assess the feasibility of 2D
gradient echo Time-of-flight (TOF) renal angiography at 7 T to detect the
arterial vasculature of the kidney and delineate the intrarenal vasculature network.
We compare TOF MRA data collected at 3 T and 7 T in the same subjects, and
illustrate the superiority of 7 T for high spatial resolution MRA.
Purpose
A substantial proportion of Chronic Kidney
Disease CKD is thought to be due to small artery disease at the
cortico-medullary border, however these vessels are too small to be imaged at
conventional MR field strengths. The superiority of ultra-high field (7T) MR Time of Flight (TOF) Angiography for visualization of the microvasculature compared with clinical MRA
images at 1.5T or 3T has been demonstrated in the brain1,2. At UHF the
longer T1 relaxation time leads to better suppression of the background
signal at a lower flip angle, whilst the signal intensity in vessels remains
constant, which combined with the increased SNR should result in higher CNR in
vessels. Therefore it should be possible to obtain higher spatial resolution
MRA images at 7T without loss of CNR compared to 3T. Here, we assess the
feasibility of TOF angiography at 7T to study small vessels in the kidneys and
compare this with data acquired at 3T.Methods
Data was collected on four subjects on both a 7 T Philips Achieva and a 3 T
Philips Ingenia scanner using a 2D gradient echo (GE) Time-of-flight (TOF) MRA in
the transverse orientation. At 7 T, an 8-channel fractionated dipole array transmit
coil with 32-channel receive elements (MRcoils, Zaltbommel, Netherlands) was
used. Power-constrained RF shimming (MLS3) was performed interactively
over one or both kidneys using in-house software4. Slices were acquired
with TR/TE 20/5.4 ms, a FOV of 230 x 230 mm2, resolution 1.5 x 1.5 x
2 mm3, requested flip angle 70°, BW 298 Hz/pixel, no parallel
acquisition, resulting in 6 slices acquired per 20 s breathhold (due to SAR
limits). Data had an interpolated in-plane resolution of 0.65 x 0.65 mm. 2D TOF
scans were repeated in 12 mm steps in the foot-head direction to ensure full
coverage of the kidney (typically requiring 6 – 8 breath-holds). At 3 T, data
was collected with matched acquisition parameters, with a flip angle of 45°
to match the tissue contrast achievable at 7 T within the SAR limits. Again MRA
acquisitions were repeated to collect data across the entire kidney. Individual
TOF scans were concatenated and for each an angiogram was generated using
maximum intensity projection (MIP) in MATLAB.Results
Figure
1 compares the MR angiography data between 3 T and 7 T, using RF shimming over
both kidneys. Here both left and right renal arteries were seen at 7 T, and
despite incomplete background suppression due to power limits at 7 T, the 7 T TOF
MRA shows superior delineation of the intrarenal vessel tree. Figures 2-4 show
the comparison between 3 T and 7 T, for 7 T data in which an MRA was collected
separately using an RF shim optimised for the left or right kidney. Qualitative image analysis reveals the superiority of 7T TOF data to
detect smaller vessels providing improved delineation of vessels from the root
(renal artery) to the peripheral branches (cortical arteries), as seen in both
the example slices and the MIP.Discussion
Previous
studies at 7 T5,6 have shown the possibility of 2D GE TOF renal MRA,
and shown that it provides superior delineation of the aorta and left and right
renal arteries compared. Here the spatial resolution was increased (1.5 x 1.5 x
2 mm) to show the delineation of small intrarenal arteries.Conclusion
The
increased SNR and longer relaxation times of 7 T provide improved delineation of
the intrarenal vasculature.Acknowledgements
This work was supported by funding from the Engineering and
Physical Sciences Research Council (EPSRC) and Medical Research Council
(MRC) [grant number EP/L016052/1].References
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