Fabian J. Kratzer1, Sebastian Flassbeck1,2,3, Sebastian Schmitter1,4, Tobias Wilferth5, Arthur W. Magill1, Benjamin R. Knowles1, Tanja Platt1, Peter Bachert1, Mark E. Ladd1, and Armin M. Nagel1,5
1Medical Physics in Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany, 2Center for Advanded Imaging Innovation and Research, New York University, New York, NY, United States, 3Center for Biomedical Imaging, Dept. of Radiology, New York University, New York, NY, United States, 4Physikalisch Technische Bundesanstalt (PTB), Braunschweig and Berlin, Germany, 5Institute of Radiology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen (FAU), Erlangen, Germany
Synopsis
Sodium relaxation times have been shown to be
altered in several diseases. Hence, 2D sodium relaxometry using Magnetic Resonance Fingerprinting (23Na-MRF) was demonstrated
recently as a proof of concept. In this work an extension to a 3D sequence is presented.
Furthermore, a more complex signal model based on irreducible spherical tensor
operators was investigated. The feasibility of simultaneous 3D quantification
of T1, T2s*, T2l*, T2*
and ΔB0 was demonstrated in phantom measurements.
Introduction
Recently the
feasibility of sodium Magnetic Resonance Fingerprinting (23Na-MRF) was
presented as a proof of concept1,2, enabling the simultaneous
quantification of T1,T2s*,T2l*,T2*
and ΔB0. Here, non-steady state conditions were generated via temporally
varying flip angles (FAs) and sequence timings to generate a unique signal
evolution for a given parameter set.
In this work, 23Na-MRF
was extended in two ways: Firstly, the coverage was changed from 2D to 3D,
allowing for simultaneous quantification of T1,T2s*,T2l*,T2*
and ΔB0 in a 3D volume within approximately the same measurement
time. Secondly, irreducible spherical tensor operators (ISTOs) were exploited for
the simulations, which allow a more sophisticated signal simulation for spin
3/2-nuclei.Methods
The 3D-radial implementation
of the previously proposed 23Na-MRF sequence1 uses a variable
non-selective excitation pulse followed by a variable echo time (Fig.1) and a
density adapted center-out radial readout3. Subsequently, a gradient
rewinder is played out and a 2π spoiler
gradient is switched along the z-direction, followed
by the next excitation pulse.
Each time frame
was acquired with 150 center-out spokes which are distributed equidistantly in
k-space, whereas subsequent time frames were rotated via the 13th tiny
golden angle4 to achieve full sampling over the entire measurement.
The dictionary simulation
was based on ISTOs as proposed by Hancu et al.5, which are based on
spectral density parameters ($$$J_0\geq J_1\geq J_2$$$),
the off-resonance ΔB0 and the residual quadrupolar moment ωq. Relaxation towards M0
was enabled6. Under the assumption that ωq is negligible, the relaxation times
can be calculated as7:
$$T_{1l}=\frac{1}{2J_2};T_{1s}=\frac{1}{2J_1} [1] $$
$$T_{2l}=\frac{1}{J_1+J_2};T_{2s}=\frac{1}{J_0+J_1} [2]$$
To
introduce the apparent transverse relaxation T2* (T2l*,T2s*
respectively) each parameter set (J0,J1,J2,ωq), with central
off-resonance ΔB0,
was simulated for an off-resonance range of $$$\overline{ΔB_0}=[ΔB_0-100,ΔB_0-99,...,ΔB_0+100]$$$ Hz.
The resulting signal evolutions were interpolated onto a 0.5Hz grid and summed along
the $$$\overline{ΔB_0}$$$-direction,
weighted with a Lorentzian distribution pL. Different T2*
values were constructed by varying the width of pL such that $$$T_2>T_2^*>0.4T_2$$$ ($$$T_{2l}>T_{2l}^*>0.6T_{2l}$$$ respectively) in 1ms steps.
The
expected signal evolution of a 23Na inversion recovery (IR) experiment
is given by:
$$S(t)=S_0(1-2(0.8e^{-t/T_{1l}}+0.2e^{-t/T_{1s}})) [3]$$
However, in literature T1 is mostly modelled
monoexponentially since the separation of T1l and T1s
based on fitting the inversion recovery signal curve is challenging. Therefore,
the first order Taylor expansion of a biexponential function with $$$a+b=1$$$ is considered:
$$ae^{\overline{a}t}+be^{\overline{b}t}=a\sum_{n=0}^\infty \frac{(\overline{a}t)^n}{n!}+b\sum_{n=0}^\infty \frac{(\overline{b}t)^n}{n!}\approx(a+b)+a\overline{a}t+b\overline{b}t=1+(a\overline{a}+b\overline{b})t\approx \sum_{n=0}^\infty \frac{((a \overline{a}+b \overline{b})t)^n}{n!}=e^{(a \overline{a}+b \overline{b})t} [4]$$
Comparison with equation [3] yields:$$$a=0.8$$$,$$$\overline{a}=\frac{-1}{T_{1l}}$$$,$$$b=0.2$$$ and $$$\overline{b}=\frac{-1}{T_{1s}}$$$, resulting in the monoexponential estimate:
$$\frac{1}{T_1}=\frac{0.8}{T_{1l}}+\frac{0.2}{T_{1s}} [5]$$
The
dictionary was simulated as follows:
1.
Set parameter space:
biexponential: T1=[20,21,…70]ms, T2l=[15,16,…60], T2s=[1.0,1.3,…14.8],
ΔB0=[-50,-48,…50]Hz;
monoexponential: T1=[30,31,…90]ms, T2=T2l=T2s=[5,6,…80]ms,
ΔB0=[-50,-48,…50]Hz
2.
Calculate T1l
and T1s using equations [1],[2] and [5]
3.
Delete parameter sets
that violate $$$T_{1l} \geq T_{2l} \geq T_{1s} \geq T_{2s}$$$ ($$$\widehat{=}J_0 \geq J_1 \geq J_2$$$)
4.
Convert parameter sets
into spectral density parameters using equations [1] and [2]
5.
Simulate signal
evolution for each parameter set
6.
Interpolate along $$$\overline{ΔB_0}$$$-axis
to a step size of 0.5Hz
7.
Sum up signal
evolutions weighted with variable pL along the $$$\overline{ΔB_0}$$$-axis
such that $$$T_{2l}>T_{2l}^*>0.6 T_{2l}$$$ (monoexponential: $$$T_{2}>T_{2}^*>0.4 T_{2}$$$)
; T2l* (T2*) in 1ms steps; central ΔB0 = [-50,-48,…,50]Hz
8.
Concatenate
biexponential and monoexponential parts
9.
Compress dictionary using
singular value decomposition (SVD) up to rank 12
The
reconstruction was performed via a low rank alternating
direction method of multipliers approach8,1.
Measurements
(resolution: 3x3x3mm3) were performed on a 7T whole-body system (Siemens,Germany) using a 23Na-birdcage
coil (Rapid,Germany).
A cylindrical phantom filled with 0.9% NaCl solution (compartment 0), containing
seven vials with additional 1%-7% agar (compartments 1-7), was imaged. A
reference T1 map was determined based on an IR sequence (sequence
parameters in Fig.2). Transverse relaxation parameters were determined by
fitting a multi-echo GRE dataset (Fig.3). The phase difference yielded
reference ΔB0 maps (Fig.2) and B1+ was measured using the
phase sensitive method9 (FA=90°;TR=185ms;TE=0.55ms). The combined reference
scan time (excluding B1+) was 7h42min, whereas the 23Na-MRF data was acquired
within 1h4min.
Mean
and SD of all quantified relaxation times were calculated in all vials for each
slice.Results
The resulting relaxation times and ΔB0
of the central slice are shown in Figs.2 and 3. All mean relaxation times obtained
by 23Na-MRF are in agreement with the reference results within the
SD (Tab.1), except for T1 in compartment 7 and T2* in compartment 1. Fig.4 displays the mean relaxation time in each
compartment in dependence on the z-position, as well as the mean B1+
averaged over the whole phantom in each slice.Discussion and Conclusion
This work demonstrates the feasibility of
simultaneously quantifying T1,T2s*,T2l*,T2*
and ΔB0 within approximately 1h by means of 3D 23Na-MRF in
combination with ISTOs for the dictionary simulation. Despite using a fairly
simple FA and TE pattern, good agreement between the results of the reference
measurements and 3D 23Na-MRF was found. The differences in T1
in compartment 7 can be explained as here strong a biexponential T1
could be present10, violating equations [4] and [5].
In compartment 1, T2*
can be described both bi- and monoexponentially almost equally well (see
Fig.3), which could explain the discrepancy between reference and MRF.
Fig.4 indicates that B1+
correction could improve the parameter quantification.
These experiments are promising as this technique
could allow full 3D-mapping of the relaxometric parameters in less than 1h.Acknowledgements
No acknowledgement found.References
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