Ke Jiang1, Wen Song1, Chao Zou1, and Yiu Cho Chung1
1Paul C. Lauterbur Research laboratory for Biomedical imaging, Shenzhen Institutes of Advanced Technology, ShenZhen, China, People's Republic of
Synopsis
We propose to acquire the different
components in the steady state signal by interleaving. Using DESS as an
example, we show that through appropriate gradient design, the two major
components (S+ and S-) in the SSFP signal can be separately acquired in
alternate TR and form images similar to those conventionally acquired by DESS.
The new technique shortens TR and reduces motion and diffusion sensitivity.Introduction
A steady state free precession signal consists
of multiple components. These components can be separately acquired within one
TR [1]. A long TR is needed to accommodate the multiple readouts, and is
unfavorable to components which are formed over multiple TR cycles. DESS (dual
echo in the steady state) is an example where the FID (S+) and spin echo (S-)
components are sampled in one TR [2]. Here, S+ increases with TR while S-
decreases with TR. The longer TR (compared to FISP or PSIF) increases the
sequence’s sensitivity to motion and diffusion. Crusher gradients must be
carefully designed to separate the two signals and minimize diffusion
sensitivity [3].
Here,
we propose to acquire the multiple components in the steady state signal by
interleaved acquisition of SSFP signal components through appropriate gradient
design using DESS as an example. In this case, we show that the two major components
(S+ and S-) in the SSFP signal can be separately acquired in alternate TR and
form images similar to those conventionally acquired by DESS.
Materials and Method
Sequence:
Figure 1 shows the proposed (three dimensional) sequence (interleaved DESS or
iDESS). The crusher dephasing S- during the acquisition of S+ is moved to the
start of the next TR cycle when acquiring S-. Properties of images formed from
the two signals remain unchanged compared to FISP and PISF. The sequence is
implemented on a 3T MRI system (TIM TRIO, Siemens, Erlangen)
Experiment: the sequence is tested on a
phantom consisting of 2 test tubes with T1/T2 values of 654.9/41.3ms,418/28.8ms. Images from the FID and SE signals acquired with iDESS are
acquired at several flip angles (10°, 15°, 20°, 25°, 30°). The signals are
compared with the images separately acquired using the FISP and PSIF sequences (using
the same flip angles) to check if interleaved acquisition affects the steady
state signal.
iDESS
is then tested in 3 healthy volunteers (IRB approved) for two applications of
DESS: knee and vessel wall imaging. Informed consents are obtained from the
healthy volunteers. High resolution knee imaging is performed in two volunteers.
A custom made knee coil was used. Imaging parameters were: flip angle 40°, FOV=200×125×96mm
3, spatial resolution=0.4×0.4×3mm
3, TR/TE=11.6/5.75ms, bandwidth =199 Hz / pixel, NEX=2, acquisition time=7.9mins, partition resolution was zero-padded to 1.5mm. High
resolution vessel wall imaging of the femoral arteries are performed in another
3 volunteers. A 16 channel body coil and the spine coil are used for reception.
Imaging parameters used were: flip angle=32°, FOV=360×180×360mm
3 , spatial resolution = 0.8×0.8×3mm
3 , TR/TE=8.54/3.36ms,bandwidth=744Hz/pixel,NEX=1,iPAT=2,aquisition time =4.2mins, partition resolution was zero-padded to 1.5mm.
Results
Figure 2 shows the results from the phantom
experiment. The S+ and S- signals acquired by iDESS and those from FISP and
PSIF using different flip angles are nearly identical.
Figure 3 shows the separate and then the
combined images of the knee obtained using iDESS. Note the bright synovial
fluid typical of DESS images of the knee.
Figure 4 shows the grey and dark
blood signal of the femoral arteries, as observed in [4]
Discussion
The study showed that components in the
SSFP signal can be separately acquired in an interleaved way. In-vivo images of
the knee and femoral arteries from iDESS have similar properties of DESS
reported. Weak components in the SSFP signal would benefit most from this
approach. While the technique may increase the SAR value, it helps reduce the
sequence’s signal loss due to the increased sensitivity to motion and diffusion
in DESS.
Acknowledgements
No acknowledgement found.References
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1991.
2. Bruder et al., Magn Res Med 7:35, 1988.
3. Bieri O et al., Magn Res Med 68:1586,
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4. Langham MC et al., Proc. ISMRM 2015,
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