Davide Piccini1,2, Peter J. Weale3, Saeed Mirsadraee4, Rachel O. Forsythe5, Annette S. Cooper6, and Scott Semple5,6
1Advanced Clinical Imaging Technology, Siemens Healthcare, Lausanne, Switzerland, 2Department of Radiology, University Hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland, 3Siemens Healthcare Ltd, Camberley, United Kingdom, 4NHS Lothian & Clinical Research Imaging Centre Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom, 5Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom, 6Clinical Research Imaging Centre, University of Edinburgh, Edinburgh, United Kingdom
Synopsis
Respiratory self-navigated 3D-radial MRA is
an efficient and robust method for the depiction of coronary luminal anatomy at
1.5T. Higher magnetic fields are more challenging, due to off-resonance
artifacts. Contrast-enhanced imaging is usually beneficial. However, variable
contrast during prolonged scans can deteriorate the self-navigation signal. Here
we investigate the use of an ultra-small super-paramagnetic iron oxide
particles (USPIO) contrast agent with longer half-life in combination with self-navigation
at 3T. Systolic and diastolic datasets from 10 volunteers were acquired and analyzed.
We show that USPIO contrast-enhanced self-navigated coronary MRA is feasible at
3T with good image quality and reliable motion correction.Purpose
Respiratory self-navigation (SN) in 3D
radial segmented MR imaging [1,2] is an efficient and robust method for the depiction
of coronary luminal anatomy using MRI when compared to more standard
navigator-gated acquisitions [3]. This method has largely been used at 1.5T in
combination with bSSFP readouts, both with and without gadolinium-based contrast
agent injection, to provide the high blood-to-myocardium contrast required for vessel
segmentation and respiratory motion tracking [4,5]. However, at higher magnetic
field strengths, bSSFP imaging is often confounded by off-resonance artifacts and
conventional gadolinium-based contrast agents combined with inversion-recovery
preparation and gradient-echo readouts often cannot achieve a constant signal
throughout the scan. Variable contrast can cause deterioration to the tracking
signal of self-navigation and therefore to the resulting motion correction.
Here we investigate the use of an intravascular contrast agent based on ultra-small
super-paramagnetic iron oxide particles (USPIO) with longer half-life as a
potential method to improve the performance of self-navigation at 3T.
Methods
In this preliminary study, N=10 healthy
volunteers were recruited in accordance with local ethical approval. Segmented,
3D ECG-triggered, respiratory self-navigated, whole-heart coronary MRA was
performed. All datasets were acquired using a prototype 3D radial sequence [6]
on a 3T clinical system (MAGNETOM Verio, Siemens Healthcare, Erlangen, Germany).
Using an empirically selected inversion time of 300ms good myocardial
suppression and appropriate enhancement of the blood pool was obtained over a
40-50min window (allowing repeat imaging if required). Sequence parameters
were: TR/TE 3.5/1.7ms, FOV (220)mm
3, matrix 192
3, voxel
size (1.15mm)
3, RF excitation angle 15° and receiver bandwidth 1000Hz/Px.
About 12000 radial readouts were acquired in 300-400 heartbeats, with an
overall undersampling ratio of 20%. Intravenous ferumoxytol (510mg of elemental iron (Fe) in 17 ml (30 mg/ml)) at a dose of 4mg of iron
(Fe)/kg of body weight was
administered over a 15min infusion (in accordance with international
guidelines). In all cases both diastolic and systolic imaging was undertaken
and evaluated for reliability of the self-navigation signal and final image
quality. Expert assessment of an experienced radiologist (SM), who graded the
Aorta (Ao), the main pulmonary artery (PA) and vein (PV), the superior (SVC)
and inferior (IVC) vena cava, and the proximal- and mid-left anterior
ascending (LAD) and right coronary arteries (RCA) was performed on a 5-point
scale: 0 = not visible, 1 = markedly blurred, 2 = moderately blurred, 3 =
mildly blurred and 4 = sharply defined. Finally, coronary vessel sharpness and
length were computed as described in [7].
Results
In almost all cases
both the SN signal and the final image quality were good (Fig.1,2) –with the only
two confounding issues observed in individual cases, 1) sub-optimal fat-saturation
reducing CNR in small vessels and 2) large non periodic motion (heavy
inspirations) in subjects with less regular respiratory pattern. The long
half-life of the contrast agent enabled an identical inversion time to be used
for both systolic and diastolic acquisitions, providing good tissue contrast
for both datasets. The tracking was successful in all 20 acquisitions. The
grades from the expert assessment were very similar between diastolic and systolic
acquisitions for the great vessels with averages of: 3.7±0.4 (Ao), 3.6±0.5 (PA), 3.3±0.5 (PV),
3.6±0.5 (SVC), and 3.5±0.5 (IVC). The average grades, sharpness, and length for
all evaluated coronary segments are reported in Fig.3. All
reported values did not show statistically significant differences between
diastolic and systolic datasets, although a trend for increased sharpness of the systolic RCA and length of the diastolic RCA could be noticed (Fig.3,4).
Discussion
The long-lasting contrast enhancement
provides a constant signal enhancement in both spatial and temporal dimensions
and enables high quality MRA acquisitions. The very high blood-to-background
contrast is ideal for the tracking of the blood pool performed by the
self-navigation algorithm, both for diastolic and systolic acquisitions. Although trends for differences in the delineation of the RCA can be noticed, no
statistical significance was reached. Potential improvements include methods
for automated rejection of data acquired during anomalous respiratory motion
[8] and further optimization of image contrast. The longer acting contrast
agent allows additional data to be re-acquired in problematic cases, while
volume rendering of the 3D datasets becomes easier due to the high contrast of
the vessel lumens (Fig.5). As USPIOs can be used as biomarker for
inflammation there is the potential to use this methodology as both an
angiographic method and as a method for detection of concentration of USPIO in
areas of inflammation.
Conclusion
We have demonstrated the feasibility of T1
shortening USPIO based contrast enhanced respiratory self-navigation for
whole-heart free-breathing coronary MRA at 3T for both diastolic and systolic
acquisitions.
Acknowledgements
No acknowledgement found.References
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