Synopsis
A
new golden angle radial arterial spin labeling acquisition method is proposed
in which labeled blood water is continuously imaged as it passes through the
large arteries and into the tissue. Both
angiographic and perfusion images can then be reconstructed from the same raw
data set at any retrospectively chosen time points and temporal resolution. This makes efficient use of the post-labeling
delay dead time to provide a more complete assessment of blood flow into the
brain, which may be of use in a variety of cerebrovascular diseases.Introduction
In
conventional arterial spin labeling (ASL)1-3, the inversion of blood water in
the neck is followed by a long post-labeling delay (PLD) to allow the blood to
reach the tissue before image acquisition, yielding perfusion contrast. ASL can also be used to generate angiographic
images4,5 if the PLD is very short. In cerebrovascular disease, information about
the status of the arteries and tissue perfusion are both crucial, but separate angiographic
and perfusion acquisitions may be unfeasible in a busy clinical protocol.
In this study a new golden
angle radial ASL imaging method is proposed in which the labeled blood is continuously imaged after
labeling, allowing both angiographic and perfusion images to be reconstructed
from the same raw data set. This makes
efficient use of the PLD “dead time” normally required in perfusion imaging,
whilst also giving a greater degree of flexibility in the image reconstruction
process, allowing the resulting images to be tailored to the hemodynamics of
each subject. A 2D multi-slice implementation is presented
here, but the same principles could apply to 3D imaging.
Methods
A schematic
of the Combined Angiography and Perfusion using Radial Imaging and ASL (CAPRIA)
sequence is shown in Figure 1. After
pre-saturation and pseudo-continuous ASL (PCASL) labeling, a spoiled gradient
echo golden angle radial scheme6 is used to continuously image the
labeled blood passing through the arteries and into the tissue. The azimuthal angle of the ith
line after the nth PCASL preparation is:$$\phi_{i,n}=(n\frac{t_{max}}{TR}+i)\,\phi_G\qquad\text{where}\qquad\phi_G=111.2^\circ\tag{1}$$where tmax
is the maximum temporal resolution desired for reconstruction. This results in relatively even coverage of
k-space when combining data within an arbitrary temporal window across multiple
PCASL preparations, thereby allowing reconstruction of angiographic images at
high temporal resolution and perfusion images at lower temporal resolution from
the same raw data set. Acquisition of PCASL
control data is interleaved with label data to minimize subtraction artefacts from
subject motion or scanner drift. Numerical
simulations of the ASL signal7, accounting for attenuation due to
the imaging pulses8,9, were used to optimize the TR and
flip angle (Figure 2).
Four
healthy volunteers were scanned under a technical development protocol agreed
by local ethics and institutional committees on a 3T Siemens Verio scanner using
a 32-channel head coil. CAPRIA data were acquired in four 10mm slices
sequentially, each taking 2.5min.
Imaging parameters were: labeling duration 1.4s, imaging time 2s, matrix
192, TR/TE 12/6ms, flip angle 7°, bandwidth 102Hz/Pixel.
For this study, angiographic/perfusion images were
reconstructed at 108/252 ms temporal resolution, respectively, using a
regridding algorithm10 and adaptive coil combination11. Perfusion images were post-hoc smoothed to boost
SNR and match typical ASL in-plane resolution (3.4mm). To give the appearance of inflowing blood in
the angiograms, “inflow subtraction” was also performed12,13. Simple
outflow timing metrics14 were calculated from angiographic images. Perfusion data were fitted to the ASL kinetic
model7 including a macrovascular component15, with T1 modified to account for the
imaging pulses8.
Results
and Discussion
The CAPRIA sequence is capable of simultaneously generating dynamic
angiograms and perfusion images, as demonstrated in Figures 3 and 4. The expected patterns of vascular filling and
tissue perfusion were observed in all subjects, in both the reconstructed
images and the derived parameter maps (Figure 5). The golden angle radial scheme is well suited
to this application, since dynamic angiograms require high spatial and temporal
resolution, but are sparse and relatively high SNR, so undersampling can be
tolerated. The converse is true of
perfusion imaging, but lower spatial and temporal resolutions are required, so more
data can be used to reconstruct each image and the denser sampling near the
center of k-space improves the reconstruction.
One additional benefit of this readout scheme is the absence of
distortion and dropout artefacts that are often observed in conventional ASL
perfusion imaging using readouts such as echo-planar imaging.
Acquisition of angiographic and perfusion images after
ASL labeling has previously been shown using two separate dedicated readouts
combined with a time-encoded preparation16. This has the advantage of allowing separate
optimization of the two readout modules, but unlike CAPRIA, the timing of the
resulting images must be decided in advance, so adaptation to the hemodynamics
of each subject is not possible retrospectively.
3D CAPRIA should be possible using an extended
golden ratio approach17. The radial
trajectory and sparse nature of angiograms would also make this a good target for
acceleration methods such as compressed sensing18. CAPRIA requires
further optimization, calibration and validation against established methods,
but it is hoped it could provide a comprehensive tool for evaluating blood flow
to the brain in diseases such as acute stroke.
Acknowledgements
Thanks to the Royal Academy of Engineering for
funding support and to Siemens Healthcare for providing the base pulse sequence
code.References
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