Thomas Lindner1, Friederike Austein1, Helena Guerreiro1, and Jens fiehler1
1Department of Diagnostic and Interventional Neuroradiology, University Hospital Hamburg-Eppendorf, Hamburg, Germany
Synopsis
This work presents a method of rapidly acquiring a T1 map to optimize background suppression in Arterial Spin Labeling to improve the signal-to-background contrast.
Introduction
Arterial Spin Labeling (ASL) is a known technique for
the non-invasive evaluation of cerebral blood flow (CBF) [1]. The technique produces
relative perfusion values by subtracting the label and control image that are
obtained in an interleaved fashion. To obtain maximum signal-to-background contrast
in the final (perfusion) image, background suppression pulses are commonly used
[2]. These pulses aim to cancel the signal of static tissue (gray and white
matter) while blood difference signal should remain maximum. The timing of
these pulses has commonly been obtained by Bloch simulations of the signal
course of tissues with values taken from the literature. This study aims to improve
background suppression pulse timing by incorporating rapid T1 mapping of static
tissue into the ASL sequence, thereby improving the final images.Materials and Methods
The test collective consists of 10 healthy volunteers
(4 women, 6 men, mean age 26.8 years). All subjects underwent scanning on a 3T
MAGNETOM Prisma scanner (Siemens Healthcare, Erlangen, Germany) equipped with a
64-channel head coil. The study was approved by the local ethical committee,
volunteers gave written informed consent. Scan parameters included: 2000ms
labeling duration and 1700ms post labeling delay, 3D GraSE readout with 3.6x3.6x4mm³
resolution, TR/TE: 400/12.06ms. The T1 maps were obtained by the variable flip
angle method using qMRLAB [3,4]. Thus, one acquisition was performed with a
single label/control pair with a flip angle (FA) of 9° for label and 20° for
control and one was acquired with the FAs switched (i.e. 20° FA for control and
9° FA for label). Acquisition of such a label/control pair took 1:12 minutes.
The “conventional” ASL acquisition was performed using 20° FA with 4
label/control pairs. Segmentation of Gray and White matter and CSF was performed
using SPM12 (The Wellcome Centre for Human Neuroimaging, London, UK). Based on
the segmented areas, a mean value of T1 was calculated and used for optimum
background suppression timing. Differences in relative (rCBF) were assessed
using the Wilcoxon-Signed Ranked test. Visual rating was performed by two
independent readers on a three-point grading scale in three categories.Results and Discussion
Using
ASL for rapid T1 mapping provided values comparable to the literature (Table
1). Adapting the background suppression pulses to the individual values show
higher signal to background ratio as compared to a fixed (standard) setting of
the background suppression pulses (Figure 1). This was confirmed by the readers
except for artifacts, which are shown to be the same in most cases, but worse
in two cases (Table 2). Differences in rCBF can be seen in table 3. These
results show a p-value of 0.05. There was no difference in results whether the
label or control condition was acquired using 9° or 20° FA respectively for mapping
(Figure 2).Conclusion
Individualization
of the background suppression pulse timing can improve the signal to background
ratio in ASL subtraction images, thus improving the visual impression. It needs
to be proven whether the scan time extension caused by adding one more
condition that cannot be used for creating perfusion images justifies the results
obtained in a clinical setting.Acknowledgements
No acknowledgement found.References
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