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Abstract
Background
Quantitative myocardial T2 mapping allows non-invasive assessment of myocardial inflammation/edema
[1]. Current implementations commonly use a T2-prepared (T2prep) SSFP sequence to
acquire different T2 weighted images at different echo times to generate the T2 maps
[2, 3]. However, all current techniques are designed for single slice acquisition
with long rest cycles (3-6 sec) after each T2prep image acquisition to allow for full
spin recovery. This markedly increases the overall scan time, especially if multiple
slices are to be acquired in serial. In this study, we propose a novel multi-slice
T2 mapping sequence, which uses slice-selective T2prep pulses combined with an interleaved
slice acquisition scheme to provide a fast multi-slice T2 mapping.
Methods
Fig. 1 shows a schematic for the proposed sequence with the proposed slice selective
T2prep pulses and the interleaved slice acquisition. Upon the acquisition of a specific
slice, the other slices are selectively prepared, excited and acquired during the
relaxation period of that slice. Thus, one T2prep image is acquired at every heartbeat.
Prospective slice tracking and retrospective image registration were used to correct
for respiratory motion. Phantom imaging was performed using NiCl2 doped agarose vials,
whose T2/T1 values spanned the ranges of values found in the blood and myocardium.
Ten healthy adults subjects (29±17 y, 4m) were imaged on a 1.5T Phillips scanner.
A free-breathing single-shot ECG-triggered slice-selective T2prep bSSFP sequence with
the following parameters was used for acquisition of five mid-ventricular short-axis
slices, FOV=320×320 mm2, in-plane resolution=2.5×2.5mm2, slice thickness=8mm, slice
gap=4mm, TR/TE=2.2/1.1ms, α=40°, SENSE rate=2, acquisition window=140 ms. For comparison,
a conventional breath-hold single-slice T2prep bSSFP sequence was performed to image
the middle of the 5-slices. All acquisitions were performed using the conventional
3-images with T2prep echo times = 0,25,50 ms (2), with a SAT image added to compensate
for the T1 relaxation time during readout [4]. T2 maps were then generated using the
3-parameter fitting model [4].
Figure 1
a) Schematic diagram of the proposed multi-slice T2 mapping sequence. Multiple single-shot
images are acquired using ECG-triggering, following T2prep of different echo lengths,
TET2P. An image, ISAT, is acquired directly after a saturation pulse to simulate the
effect of a very long T2prep echo time b) The slice selective T2prep pulse consists
of a tip-down slice selective 90˚ pulse, followed by four non-selective 180˚ refocus
pulses (only two are illustrated in the figure) and ends with a closing tip-up slice
selective 90˚ pulse. c) Slices are acquired in an interleaved fashion to allow sufficient
T1 recovery time for each slice. The slice selective 90˚ pulses are applied with a
slice thickness twice as imaging slice to minimize the impact of slice imperfection.
Results
Fig. 2a shows the correlation between T2 measurements using the single and multi-slice
sequences in phantom compared to spin echo. Figure 2b. shows an example T2 maps. Fig.
2c. shows a comparison between T2 maps generated using the single slice and multi
slice sequences. The average scan time was 20 heartbeats for the 5 slices using the
multi-slice and 13 heartbeats per slice using the single slice sequence. The average
T2 across the myocardium and over all healthy subjects was 51ms and 48ms using the
single and the multi-slice sequence respectively (p=0.1).
Figure 2
a) Correlation between T2 measurements measured in different phantoms using the spin
echo sequence and single and multi-slice T2 mapping b) A representative example for
the multi-slice T2 maps in a healthy subject. c) Two example comparisons for T2 maps
generated using the middle slice in the multi-slice acquisition and the corresponding
single slice acquisition. The bullseye shows the mean ± standard deviation of T2 in
each segment .The center values shows the mean T2 for all 5 slices.
Conclusions
The proposed multi-slice T2 mapping pulse sequence allows myocardial T2 measurements
over the entire left ventricle by imaging of 5 interleaved slices in 20 heartbeats.
Funding
N/A.
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