Evita Wiegers1, Alex Bhogal1, Sarah Jacobs1, Mark Gosselink1, Jeanine Prompers1, and Dennis Klomp1
1Radiology, University Medical Center Utrecht, Utrecht, Netherlands
Synopsis
Short TE STEAM is an
appealing MRS sequence especially for the quantification of low-concentration
J-coupled spin systems. However, in comparison to sLASER, STEAM is associated
with larger chemical shift displacement errors in all three directions. With an
inhomogeneous B1+-field, slice profiles degrade, resulting
in artefacts from extracranial lipids. Here we demonstrate that lipid
artefacts can be removed through the use of an external crusher coil. Without use
of the crusher coil, large extracranial lipid artefacts are present when
selecting a large voxel. Upon activation of the crusher coil, these signals are
eliminated, yielding 1H spectra free of large baseline distortions.
Introduction
MRS of the human
brain at 7T enables the identification of a large number of metabolites, with
increased spectral resolution and SNR compared to lower field strengths.
Typically, artifacts associated with lipid signal contamination from extracranial
sources are an issue when performing spectroscopic imaging, but lipids can also
be a problem in single-voxel acquisitions. Particularly in cases where the
voxel size must be increased for sufficient SNR to detect low-concentration
metabolites such as glutamine and glutathione (GSH). Here sequences with short echo
time (TE) are beneficial as they reduce T2-mediated signal loss,
limit the J-coupling evolution for coupled spin systems, and are generally
assumed to reduce quantification errors1.
The STEAM sequence is
suited for acquiring short TE spectra but, when using volume transmitters with
typically a lower B1+, it suffers from large chemical
shift displacement errors, which worsen with increasing field strength. Moreover,
the slice profile of the radio-frequency pulses (RF) used for localization depends
on the B1+ field and may excite extracranial lipids outside
the voxel of interest, where B1+ levels can substantially
deviate, leading to contamination.
One possible solution
is the use of outer-volume suppression pulses; however, these will increase
overall power-deposition (and thus repetition time (TR)), require slice by
slice B1+ calibration and suffer from their own
limitations with respect to spatial profile. To address the issue of lipid
contamination for short TE single-voxel MRS, we propose the use of a
crusher coil generating an external suppression field2.Methods
A
7T MRI scanner (Philips, Best, the Netherlands) was used, equipped with eight
transmit/receive 1H antennas, combined with a 32-channel receive array (Nova Medical, Wilmington, United States).
STEAM 1H MRS data (TE 7.8 ms, TM 30 ms, TR 3000 ms, NSA 32, VAPOR
300 Hz, voxel size 30x50x30 mm3) was acquired in a healthy volunteer
(male, 47 years). B1+ and B0 shimming were
performed on a manually drawn region of interest (ROI) in the frontal lobe. The
STEAM voxel was planned in a region containing the pre-frontal cortex and care
was taken not to include any extracranial lipids.
Lipid suppression was
performed using an external coil that was placed inside the 32-channel receive
coil. This coil was driven by the Z3 (third order) shim amplifier,
controlled using a dynamic shim updating unit (DSU: RRI, Billerica, USA ). Two
TTL pulses (6 ms before and 3 ms after the top of the last STEAM pulse) were
added to the STEAM sequence to activate and deactivate the crusher coil,
respectively. The crusher coil pulsed with a 3A current over 9 ms per TR
(Figure 1). Lipid suppression was checked qualitatively by applying comparable
crushing fields during the acquisition of a 2D FFE image (Figure 2). STEAM
spectra were recorded from the same voxel with and without activating the
crusher coil.Results
Figure 3 shows the B1+ map
after B1+ shimming, clearly indicating substantial differences
in B1+ inside and outside (e.g. at the skull) the shimmed
ROI in the frontal lobe, which can affects the slice profile. Figure 4 shows 1H
STEAM spectra for several receive channels without and with the use of the
crusher coil. Extracranial lipid artefacts can be found in many of the receive
channels without crushing, while they are greatly reduced with crushing. Figure
5 shows the channel-combined spectra without and with the use of the crusher
coil. Without crushing, large extracranial lipid artefacts are present, making
reliable signal quantification impossible. Upon lipid suppression with the
crusher coil, the lipid signals are to a great extent eliminated, yielding a spectrum
free of large baseline distortions.Discussion and Conclusion
Short TE single-voxel
1H MRS at 7T is appealing especially for the quantification of
low-concentration, J-coupled spin systems. Unfortunately these sequences are
susceptible to corruption from lipid artefacts. In this work, we demonstrate
that lipid artefacts can be removed through the use of an external suppression
field generated by a crusher coil. Acknowledgements
No acknowledgement found.References
1. Wilson, M, Andronesi, O, Barker, PB, et
al. Methodological consensus on clinical proton MRS of the brain: Review
and recommendations. Magnetic Resonance in Medicine. 2019; 82, 527–550
2. Boer, VO, Van De Lindt, T, Luijten, PR & Klomp, DWJ. Lipid suppression
for brain MRI and MRSI by means of a dedicated crusher coil. Magn. Reson.
Med. 2015; 73, 2062–2068