Jeffrey Visser1, Aaron Oliver-Taylor2, Tom Hampshire2, Juan Antonio Hernandez-Tamames3, Marion Smits3, Xavier Golay2,4, and Esther Warnert1
1Radiology & Nuclear Medicine, Erasmus MC, Rotterdam, Netherlands, 2Gold Standard Phantoms Limited, London, United Kingdom, 3Department of Radiology & Nuclear Medicine, Erasmus MC, Rotterdam, Netherlands, 4University College London, London, United Kingdom
Synopsis
Arterial Spin Labeling (ASL) is a magnetic resonance imaging
(MRI) technique for measuring cerebral blood flow (CBF). Here, we present data
on the reproducibility of measuring CBF with time-encoded multi post-labeling
delay (PLD) pseudo-continuous ASL (pCASL) in a healthy volunteer compared to a
flow phantom. This work shows the potential of using a flow phantom to assess
the reproducibility of quantified CBF with ASL.
Introduction
Arterial Spin Labeling (ASL) is a magnetic resonance imaging
(MRI) technique for measuring cerebral blood flow (CBF)
1. Quality assurance of
the quantification of CBF measured with ASL is of utmost importance for any
study in which these measurements are compared between different scan sessions, especially in longitudinal studies. We are investigating the use of a novel
production prototype ASL perfusion phantom system (QASPER, Gold Standard
Phantoms Limited, London UK)
2 for quality assurance of ASL in the clinical
setting. Here, we present data on the reproducibility of measuring CBF with
time-encoded multi post-labeling delay (PLD) pseudo-continuous ASL
(pCASL).
Methods
All pCASL scans were performed on a 3 Tesla MRI scanner and
with a 32-channel head coil (General Electric, Chicago, USA). Acquisition parameters for the pCASL scans
include: 3D spiral read-out, time encoded labeling, seven effective PLDs from
0.8 to 2 s, reconstruction matrix 128x128x42, resolution 1.9x1.9x3.5 mm3.
Within-session reproducibility of the pCASL scan in a healthy volunteer
(female, 31 years) was assessed: two pCASL scans were collected back-to-back,
at the beginning of this scan session, and one at the end (approximately 45
minutes after the second scan). This scan session was repeated two weeks later,
at the same time of day. To assess the reproducibility of the pCASL scans for
QASPER, we used a range of flow
velocities (350, 400, and 450 ml/min, pseudo-randomly) through the phantom.
Within-session reproducibility for all velocities was assessed by back-to-back repeating
the scans per flow velocity. Between-session reproducibility was assessed by
repeating the scan session 7 days later. The flow rates of QASPER during the
pCASL scans were set and recorded by software provided with the phantom.
Data analysis was done with in-house written MATLAB (R2016b)
scripts. The ASL difference images were quantified by least-squares fitting of
the Buxton model, accounting for the different effective label durations and
PLDs within the pCASL sequence3,4. The region of interest (ROI) for the healthy
volunteer was a whole brain grey matter mask, obtained from a high-resolution T1-weighted
image. This image was linearly registered to the ASL scans (FLIRT within FSL
5.0.9), segmented (FAST within FSL
5.0.9) to obtain the ROI. The ROI used to analyze the flow phantom data was created
as a ring, on a single slice within the perfused area in QASPER (visual inspection).
This mask was created for each scan day separately. Examples of the acquired
images for the phantom can be seen in Figure 1.
Results
The flow rate of the phantom was stable during the scans,
with variations around the set point < 1% for all three set flow velocities
on both days (Figure 2). Examples of the acquired dM/M0 values across the
perfusion region of interest for each of the flow settings can be seen in Figure
3. The average grey matter CBF for the healthy volunteer and for each of the
flow rates set in the phantom can be seen in Figure 4.The within- and
between-session coefficients of variation of the grey matter CBF of the
volunteer were higher than for the flow phantom with a set flow rate of 400
ml/min (Figure 5). Discussion
The reproducibility of CBF quantification with the phantom is
dependent on the flow velocity set for the scan. As can be seen for the flow rate
set to 350 ml/min it is not yet trivial to obtain consistent CBF measurements
with QASPER (Figures 4 and 5), which can be due to inconsistent placement of
the labeling plane as well as to air bubbles trapped within the flow phantom.
However, when using the perfusion and reproducibility results of the phantom with
a flow rate of 400 ml/min, it may be suggested that the variation measured in
the grey matter CBF of the healthy volunteer is, at least in part, a result of changes in physiological state of
the volunteer. To summarize, this work shows the potential of using a perfusion phantom to assess the reproducibility of quantified CBF with ASL. Acknowledgements
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