Karl Landheer1, Ralph Noeske2, Michael Garwood3, and Christoph Juchem1,4
1Biomedical Engineering, Columbia University, New York, NY, United States, 2GE Healthcare, Berlin, Germany, 3Center for Magnetic Resonance Research and Radiology, University of Minnesota, Twin Cities, MN, United States, 4Radiology, Columbia University, New York, NY, United States
Synopsis
A previously developed magnetic
resonance spectroscopy method is improved upon which is now able to obtain
spectra with an echo time as short as 4 ms, while recovering the entirety of
the available magnetization. This method obtains full 3D spatial localization
through a 2D adiabatic inversion pulse which is cycled “on” and “off” every
other repetition, in combination with a slice-selective excitation pulse. Both
1D and 2D spectra with an ultrashort echo time of 4 ms are demonstrated at 3T.
High quality spectra were obtained for all experiments.
Introduction
It was recently recommended in a
consensus paper to use the shortest TE achievable for general-purpose
spectroscopy[1]. To obtain both a short echo time and
full recovery of the signal a sequence referred to as SPin ECho, full Intensity
Acquired Localized[2] (SPECIAL) was developed. Although
SPECIAL provides a very short echo time it still employs a slice-selective
refocusing pulse in a single spatial dimension, which introduces anomalous J-modulation[3], [4] and chemical shift displacement error
(CSDE). As such SPECIAL-sLASER was developed which replaced the amplitude-modulated
180° refocusing pulse with an adiabatic refocusing pulse pair, but comes at the
cost of a minimum TE of 19 ms at 3T[5].
The
proof-of-principle of a sequence we now refer to as Ultra short echo TimE
SPECIAL (UTE-SPECIAL) was previously demonstrated[6], however it suffered from severe
lipid contamination rendering the spectral quantification challenging. This
abstract improves upon the previously developed sequence to obtain high quality
spectra free of erroneous signal contributions. This was achieved by: 1) replacing
the refocusing pulse by a hard pulse, thereby enabling the new ultrashort echo
time of 4 ms, 2) using an optimized phase cycling scheme to reduce lipid
contamination, 3) applying OVS in-between the preinversion pulse and excitation
pulse to reduce out-of-voxel contamination. The measured spectra are now free
from any obvious artefacts and can readily be quantified. Additionally, the
method is extended to 2D spectroscopy and J-resolved
spectra were acquired both in a phantom and a healthy volunteer. Methods
The UTE-SPECIAL sequence operates by
employing a two-dimensional selective adiabatic inversion pulse[7] followed by a slice-selective
excitation pulse and a hard refocusing pulse (Figure 1). The 2D inversion pulse
consists of 30 spiral jinc subpulses with 5-turn spiral, and the amplitude and
phase of the consecutive subpulses are modulated according to a hyperbolic
secant envelope[8] with a total duration of 40 ms and a
center frequency of 2.7 ppm. A two dimensional Bloch simulation of the
adiabatic inversion pulse was performed to demonstrate the efficacy of the pulse.
An optimized crusher and 32-step cogwheel phase cycling scheme[9] were designed with DOTCOPS[10], [11].
All experiments
were performed with a standard 48-channel head coil on a Signa Premier MRI
system (GE Healthcare, WI, USA) at the New York State Psychiatric Institute
(NYSPSI). All spectra were acquired with a TR of 2.0 s, 64 excitations and a
cylindrical voxel with size of 5.8 x 5.8 x 2.0 cm3 (5.8 cm diameter
in the inversion dimensions), and used VAPOR[12] for water suppression, as well as
outer-volume suppression (OVS) for sideband suppression. Phantom
experiments were performed on the GE MRS “braino” phantom[13].
A total of
5 male subjects were scanned, with multiple experiments being performed in some
subjects. All subjects provided free and informed consent and all
studies were approved by the IRB at Columbia University. Voxels were placed in either the
frontal or parietal lobe. All subjects had spectra acquired with TE = 4 ms. Spectra
were quantified with INSPECTOR[14] using basis sets simulated in MARS[15] using creatine as an internal
reference assuming a concentration of 8.00 mmol/kg. J-resolved spectra were obtained both in the braino phantom and in
vivo and were acquired by incrementing TE from 4 ms to 202 ms in 100 steps with
8 averages per echo time.Results and Discussion
The 2D inversion pulse provides
>99% inversion over 2.0 to 4.0 ppm and >97% inversion over 1.0 to 4.5 ppm.
Bloch simulation of the 2D
adiabatic inversion pulse demonstrates the high uniformity within the voxel with minimal sidebands
(Figure 2 a), aside from large side bands at about 25 cm distance radially from
the center of the voxel, which are outside the subject’s head for all
volunteers. This was similarly
demonstrated experimentally by imaging the voxel (Figure 2 b-g). Due to
the subpulses being of very short duration (and thus high bandwidth) there is
negligible CSDE in these two spatial dimensions (Figure 3).
High
spectral quality was demonstrated in all volunteers (Figure 4), however large macromolecule
signals can be observed be observed in all volunteers, particularly for
Experiment 2. This is not, however, believed to be artefactual, as subjects do
not demonstrate any spurious echoes in the macromolecule region, as evident by
the lack of increased deviation in this region. The mean (± standard deviation)
concentrations were measured to be 3.10 ± 0.29 mmol/kg, 2.74 ± 0.34 mmol/kg, 1.59 ± 0.23 mmol/kg, 7.63 ± 0.82 mmol/kg, 10.56 ± 1.40 mmol/kg, and 4.87 ± 0.56 mmol/kg, for total choline,
γ-aminobutyric acid, glutathione, glutamate + glutamine, N-acetylaspartic acid
and myo-inositol, respectively. J-resolved
spectra for both phantom (Figure 5 a) and in vivo (Figure 5 b) demonstrate the sequence’s
lack of unresolved peaks,[16] particularly noticeable in the
phantom lactate signal, due to the lack of slice-selective refocusing pulses.Conclusions
A novel sequence was improved, referred
to as UTE-SPECIAL, which now obtains high quality 3D localized spectra at the
ultrashort echo time of 4 ms on a clinical 3T MR scanner, full intensity
signal, adiabatic localization in two of the three spatial dimensions, no
anomalous J-modulation and minimal CSDE.
Quantification yielded results consistent with the literature.Acknowledgements
Special
thanks to New York State Psychiatric Institute (NYSPI) and Dr. Feng Liu for
their facilities and technical support and Martin Gajdošík, PhD, for fruitful
discussions and input. This work
was supported by the National Multiple Sclerosis Society (NMSS, RG-5319) and by NIH grant P41 EB027061.References
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