Bragi Sveinsson1, Garry Gold1, and Brian Hargreaves1
1Stanford University, Stanford, CA, United States
Synopsis
The double-echo in steady-state (DESS) sequence offers
both 3D anatomical imaging and 3D quantitative mapping (SNR-efficient 3D maps
of T2 and apparent diffusion coefficent) in various applications, such as breast
imaging or knee cartilage imaging. The
complicated signal behavior remains a challenge for quantitative imaging, and strong
spoiling can lead to motion artifacts. Here, we introduce simplified methods
for modeling DESS signals, enabling more accurate T2 measurements and better
motion artifact reduction.Purpose
To demonstrate the use of new models of the
double-echo in steady-state (DESS) signals to quantify T2 and reduce motion
artifacts.
Theory
The DESS sequence produces two echoes S1
and S21,2,3, before and after a spoiler gradient respectively,
which provide morphological images and have also been used for quantification
of T2 and ADC4,5,6 in cartilage. The signals have very
complicated contrast due to the contribution of multiple echo paths to each
signal7. The simple relationship $$$
\frac{S_2}{S_1} = e^{-\frac{2(\mathrm{TR}-\mathrm{TE})}{T2}}$$$
[1] has
previously been used for T2 estimation4, but underestimates
T2.
We propose a
more accurate model based on Extended Phase Graphs7, which can be
derived by tracing the echo paths between the signals S1 and S2,
and neglecting all paths that have been dephased by two or more spoiler
gradients, as shown in Figure 1:
$$ \frac{S_2}{S_1} = e^{-\frac{2(\mathrm{TR}-\mathrm{TE})}{T2} - \left( \mathrm{TR}- \frac{\tau}{3} \right) \Delta k^2 D} \sin^2{\left( \frac{\alpha}{2} \right)} \left(\frac{1 + e^{-\frac{\mathrm{TR}}{T1} - \mathrm{TR} \Delta k^2 D}}{1 - \cos{\alpha} e^{-\frac{\mathrm{TR}}{T1} - \mathrm{TR} \Delta k^2 D}} \right) = e^{-\frac{2(\mathrm{TR}-\mathrm{TE})}{T2}} \sin^2{\left( \frac{\alpha}{2} \right)} \left(\frac{1 + e^{-\frac{\mathrm{TR}}{T1}}}{1 - \cos{\alpha} e^{-\frac{\mathrm{TR}}{T1}}} \right) \hspace{2em} [2] $$
where the
gradient has magnitude G and duration τ, inducing a phase of Δk = γG τ, and D
is the diffusivity. The last step applies for small spoilers. Figure 2 shows a comparison between Eqs. 1 and
2, and a simulation of the true signals, as well as T2 estimate error. Using Eq. 2 enables better T2
estimation in cartilage by assuming the prescribed flip angle of the scan and a
typical T1 value of cartilage. Note the low sensitivity to T1,
so small errors in the T1 assumption should not cause large errors
in estimated T2. Furthermore,
for example in knee cartilage T1 does not change much where T2
is sensitive to degeneration.
Alternatively,
different echo paths between S1 and S2 can be traced exactly
to form a simple relationship of the form:
$$ S_1 = a S_2 + S_{SP} \hspace{2em} [3]$$
where $$$ a = \frac{e^{-\frac{\mathrm{TR}}{T1}} - \cos{\alpha}}{1 - \cos{\alpha} e^{-\frac{\mathrm{TR}}{T1}}} e^{-\frac{2\mathrm{TE}}{T2}} $$$ and $$$S_{SP}$$$
is an RF-spoiled signal.
Since Eq. 3 has no dependency on diffusion or
the gradient, changing the spoiler area will move a DESS data point (S1,S2)
along a line between a minimally spoiled DESS scan and an RF spoiled scan, as
shown in Fig. 3a. DESS scans with large spoiling, often run for diffusion
weighting, can deviate from this line due to motion, as shown in Fig. 3b. By
projecting the motion-corrupted points to the closest point on the line, motion
ghost artifacts can be reduced.
Methods
A DESS scan
was run in the knee of a healthy volunteer with flip angle α = 18° and a minimal
spoiler, giving very little diffusion weighting. Spin echo (SE) scans were run for
comparison with multiple echo times. T2 maps were generated using Eqs.
1 and 2 assuming Δk = 0, a typical T1 of 1.2s, and from a monoexponential
fit of the SE scans.
To demonstrate the artifact reduction from Eq. 3 in ADC estimation, two DESS scans were performed in the knee of a volunteer
using spoiler areas of 156.60 and 15.66 mT/m ms and α = 35°, with fat
suppression. An RF-spoiled gradient-echo scan was also run with the same
parameters. The strongly spoiled scan was projected to the line between the
weakly spoiled DESS scan and the RF-spoiled scan. EPI DWI scans were also run
for comparison.
Results and Discussion
The T2
maps are shown in Figure 4. Equation 1 gives an average T2 estimate
of 23.3ms in the cartilage. Equation 2 gives an average of 32.7ms, agreeing
better with the SE average of 36.8ms. The newer model clearly depicts regional
variation in the cartilage more closely to SE.
The effects on the ADC quantification are shown in Figure 5. Using Equation 3 changes the mean ADC estimate from 1.02μm2/ms to 1.43μm2/ms, which is closer to the (distorted) EPI DWI estimate of 1.54μm2/ms.
In this work, the prescribed flip angle was used in Equation 2, but this could be made even more accurate by collecting a flip angle map, giving a better estimate of the true flip angle at each pixel. The models could allow for many other types of analysis, such as estimation of flip angle or T1, and could be solved together for an expression of the individual signals.
Conclusion
Simple, yet highly accurate models of the
signals in DESS allow for reliable T
2 estimates from a single DESS scan and
motion artifact reduction in DWI using an RF spoiled scan for reference.
Acknowledgements
NIH R01-AR063643, R01-EB0002524, and K24-AR062068
GE Healthcare
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