Rebecca Emily Feldman1 and Priti Balchandani1
1Translational and Molecular Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States
Synopsis
High field MRI permits us to leverage increased
signal-to-noise ratio (SNR) and spectral separation between metabolite peaks
for more sensitive metabolite detection at higher spatial resolutions. However,
the acquisition of high-resolution spectral grids can be prohibitively time
intensive. Accelerated MRSI acquisitions are challenged by the limitations at 7T.
We develop a multi-region SPSP excitation pulse and use it to create a novel
low power, B1 insensitive multi-region SASSI sequence with minimal chemical
shift to enable accelerated MRSI.
Introduction
Magnetic
resonance spectroscopic imaging (MRSI) may be used to non-invasively measure
spatially varying metabolite concentrations in
vivo. High fields such as 7 Tesla (7T) permit us to leverage increased
signal-to-noise ratio (SNR) and spectral separation between metabolite peaks
for more sensitive metabolite detection at higher spatial resolutions. However,
the acquisition of high-resolution spectral grids can be prohibitively time
intensive. The recent development of
techniques aimed at accelerating MRSI acquisitions1,2 remain challenged by
the limitations at 7T, namely chemical shift (CS) artifacts, power (SAR)
limits, and B1 inhomogeneity. The semi-adiabatic spectral spatial
spectroscopic imaging (SASSI) sequence3 uses a spectral-spatial (SPSP) excitation
pulse and two adiabatic SPSP refocusing pulses to overcome B1
inhomogeneity, CS artifacts, and SAR limits to excite a volume of interest
(VOI) for 7T MRSI. In this work, we develop a multi-region SPSP excitation
pulse and use it to create a novel multi-region SASSI sequence to enable
accelerated MRSI. Phantom results demonstrate effective multi-region
spectroscopic grid acquisitions at 7T. Methods
We
used the adiabatic SLR algorithm4 to create a SASSI refocusing pulse and
designed a non-adiabatic SPSP excitation pulse of matching bandwidth (BW). The
excitation pulse had BW= 1.20 kHz and t=4.2 ms. The refocusing pulse had BW=1.12
kHz and a t=7 ms. Figure 1 shows the RF and gradient waveforms for the multi-region
SASSI pulse sequence. A multi-band excitation pulse was created by designing
individual pulses for each spatial location and combining them with phased
complex addition. Figure 3 is a simulation of the signal with the modified excitation
pulse is shown in along with a simulation of the sensitivity of the spatial
profile to a range of B1 values to determine sensitivity to B1
inhomogeneity. Scans were performed on a spherical MRS phantom using a 7T whole
body magnet (Siemens) and a 32-channel receive head coil. To acquire the
spectral grids and metabolite maps, the pulse sequence parameters were: spectral
shift=-2.82 ppm, TE=42 ms, TR=1000 ms, time=20 minutes. For SAR comparison, spectra were acquired in
a phantom using multi-region SASSI and a standard single-VOI Semi-LASER
(sLASER)6. SAR in the phantom was recorded for each acquisition relative to
sLASER for a long TR, low-resolution scan chosen in order to reach the upper
limit of SAR in the sLASER sequence. The pulse sequence parameters for both
sLASER and SASSI for the SAR comparison were: spectral shift=-2.82 ppm, TE=42
ms, TR=2530 ms, time=30 minutes. Metabolite fitting and integration under peaks
was performed using LCMODEL7 to obtain concentrations of myo-inositol (MI),
N-acetyl aspartate (NAA), Choline (Cho), and Creatine (Cr). Results
The simulation of the SPSP profile of the multi-region SASSI
excitation (Figure 3) shows two clear excitation planes. While a conventional,
dual spin echo pulse would see a 50% loss in signal over a 24% change in B1;
the loss in signal for multi-region SASSI for that same B1 change is
8%. SAR relative to the sLASER sequence (at 100%)
was 36% for the multi-region SASSI.
On the right region, the ratio of NAA/Cr was
1.42. On the left, the ratio of NAA/Cr was 1.45. The metabolite maps of NAA, Cho,
and Cr, acquired in cross-section to highlight the two regions, are shown in
Figure 5. Chemical shift in the ROI was not detectable.Discussion
Creating
an excitation pulse capable of exciting two slices simultaneously resulted in a
SPSP excitation pulse with higher peak power and higher overall SAR than a
single region excitation pulse. However,
in the SASSI sequence, the non-adiabatic excitation contributes significantly
less power than either of the adiabatic refocusing pulses, and therefore has some
room for amplification. A similar modification of the spatial sub-lobes could
be applied to either of the adiabatic pulses. However, the resulting sequence would
deposit higher SAR without an increase in B1 insensitivity. The
proposed multi-region SASSI is significantly less SAR intensive than other
adiabatic MRSI sequences such as sLASER, making it a suitable candidate for
augmentation into a simultaneous multi-region acquisition. Conclusion
We
designed and implemented a low-SAR semi-adiabatic MRSI sequence capable of
exciting multiple regions. The sequence retains the B1-insensitive
volume selection and low chemical shift of SASSI while creating two spatially
separated volumes of interest that could be acquired at the same time. Future
work will combine this multi-region spectral excitation with parallel imaging
and reconstruction techniques to simultaneously excite and disentangle multiple
regions. This will provide an accelerated MRSI sequence with higher B1-insensitivity
and reduced SAR, thereby providing a powerful alternative for high-resolution
spectroscopic acquisition to measure and detect metabolic alterations
associated with many diseases and disorders7,8,9,10.Acknowledgements
NIH R01 MH109544; Icahn School of Medicine Capital Campaign, Translational
and Molecular Imaging Institute and Department of Radiology, Icahn School of Medicine at Mount SinaiReferences
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