Guodong Weng1, Claus Kiefer1, Irena Zubak2, and Johannes Slotboom1
1Institute for Diagnostic and Interventional Neuroradiology, Support Center for Advanced Neuroimaging (SCAN), University of Bern, Bern, Switzerland, 2Department of Neurosurgery, Inselspital Bern and University Hospital, Bern, Switzerland
Synopsis
To overcome the B1+ inhomogeneities and SAR limitation for using MRSI-editing at UHT (≥7T), a new spectral editing scheme was developed within an EPSI sequence for whole brain MRSI. The slice-selective refocusing pulse was replaced by a chemical-selective adiabatic 2π-refocusing pulse pair with varying passbands. The results show an excellent glutamate, 2HG and GABA-editing pattern with in vitro and in vivo measurements. This study has shown the excellent performance of the proposed new spectral editing scheme, and proved that it could be an alternative method for MEGA editing.
INTRODUCTION
Due to better its better SNR,
localized spectroscopy is predestined for application at ultra-high file (UHF) (≈7T). In practice, however, many hurdles related to
the underlying physics, have to be overcome. Apart from SAR ($$$ \propto $$$B02),
the wavelength of the EM-wave (≈11cm at 7T) is shorter than the
anatomic structures to be examined which often results in severe interference
patterns (inhomogeneities) in the B1+. The B1+-inhomogeneities
can partially be overcome by the use of adiabatic RF-pulses 1 or with parallel transmit
techniques 2. However, due to practical limitations
on the maximum available B1+ and the relatively high SAR of adiabatic
spatial selective refocusing pulses, their number should be kept as low as
possible. Additionally, their high SAR sets clear limits the practical
available RF-bandwidth ($$$ \Delta \omega_{RF} $$$) drastically, which in its turn promotes
the chemical shift displacement artifact CSDA 3. However, larger $$$ \Delta \omega_{RF} $$$ is needed in UHF MR-spectroscopy applications since $$$ \Delta \omega_{RF} \propto B_0$$$. Spectral editing for
the detection of e.g. 2HG or GABA is a technique that can be combined with
volume localization schemes by adding MEGA editing-pulses 4 adding additional SAR to the
sequence. Many MEGA implementations use pure amplitude modulated Gaussian
shaped p-pulses,5,6 whose editing performance suffers
at high field from severe B1+ inhomogeneities in the
clinical 1Tx mode. Therefore, an adiabatic MEGA-editing scheme was developed in
1D-semiLASER (Localization by Adiabatic SElective Refocusing) sequence 7. This abstract proposes a new
editing scheme completely different than MEGA which we integrated into EPSI 8 allowing for whole brain 2HG or
GABA edited EPSI-MRSI. The novel editing method will be further referred to as SLOW,
in analogy to MEGA. SLOW consists only of 2 RF-pulses: apart from a slab
selective RF-excitation pulse, only one
chemical shift selective adiabatic 2π-pulse with varying passbands. The
general properties of single shot EPSI-sequence using 2π-pulses
are described in a separate abstract. This
abstract focuses on the editing properties of variable bandwidth 2π-pulses. METHODS
Figure 1 below shows the adapted
EPSI pulse sequence, in which the original slice selective refocusing pulse was
replaced by an adiabatic complex secant hyperbolic RF-pulse pair $$$ B_1^+(t) = \Omega_0 \cdot sech(\beta
t)^{1+\mu i} $$$ 9 selectively refocusing two
different offset frequency ranges mimicking editing “off” and “on” of MEGA-typed editing. In SLOW-editing we refer
“editing-off” as “editing full” and “editing-on” as “editing-partial. In analogy
to MEGA-editing, the type of editing is further referred to SLOW-editing. In
vitro tests were carried out on three spherical phantoms (1.) brain metabolite
phantom (GE), (2.) home-build 2hydroxyglutarate (2HG)-phantom (~7.8 mmol/L of
2HG and 18 mmol/L of glycine), and (3.) home-build GABA-phantom (~10 mmol/L of
GABA, creatine, and glycine). In vivo test was performed on one
healthy volunteer. All measurements were performed on a 7T MAGNETOM Terra
MR-scanner (Siemens, Germany) in clinical-mode.
In Figure 2a the frequency
selective refocusing offset frequency ranges are displayed for the 2HG-edited SLOW-EPSI
whole brain MRSI. During the first acquisition the whole spectrum from 1.8 ppm
till 4.2 ppm is refocused (denoted by editing-full), whereas the second echo is
obtained refocusing the 0.8 ppm till 3.2 ppm range (denoted by editing-partial). Like in MEGA-editing, SLOW-editing also
required the two responses to be subtracted.
As a second example of SLOW-editing
GABA editing can be similarly be performed by selectively refocusing the 1.65 ppm-4.2
ppm during editing “full” and 2.7 ppm till 4.2 ppm editing “partial” phase. RESULTS AND DISCUSSION
Figure 2b-d shows the in vitro
result of SLOW-editing for different echo times. As expected, the editing
effect shows a clear TE-dependence, indicating that the TE=120ms may be the
optimal TE for 2HG-detection at 7T.
Figure 3 shows the EPSI-SLOW pulse
sequence applied on a phantom containing the main brain metabolites, however no
GABA. The SLOW-full refocuses the offset range between 1.65-4.2 ppm whereas the
SLOW-partial refocuses 2.7-4.2 ppm range. The difference spectrum very nicely
shows the editing effect on glutamine/glutamate multiplet at approximately 3.75
ppm.
Figure 4
shows the effect of SLOW-editing on a GABA and glycine and creatine containing
phantom.
Figure 5
shows the in vivo results of the SLOW-EPSI editing sequence for various TE in
the range [68 – 110 ms]. The displayed the sum volume of 3 voxels being 13 X 11
X 15 mm. The optimal TE for GABA editing was 68 msec, confirming the in vitro
results of Figure 4.
CONCLUSION
SLOW-editing has been presented
which is an alternative method for spectral editing using MEGA editing based on
adiabatic 2π-pulses and was integrated into a 3D-EPSI pulse sequence
and tested at 7T. Since this pulse sequence requires only one slab selective excitation
pulse and one adiabatic chemical shift selective 2π-pulse
having variable passbands for editing the SAR can be kept extremely low. In
contrast to MEGA-editing, SLOW-editing uses adiabatic refocusing and is
therefore robust toward B1+-inhomogeneities which are
inherent at UHF MRI/MRS. Finally, due to the use of the small band chemical
shift selective adiabatic 2π-pulse, there is no in-plane CSDA,
and a minimal CSDA perpendicular due to slab selective excitation pulse. Acknowledgements
This work was supported by the Swiss National Science Foundation grant number 182569. Additionally, this project has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No 813120.References
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