Application of 7T MRS to High-Grade Gliomas

3T/7T MR imaging data, 7T SVS data, and LCModels from a patient with diffuse glioma are presented (TR/TE for the 7T SVS data = 8500/6 ms), with tumor data on the left (blue arrow) and peritumoral data on the right (green arrow) for each patient. Inspection of the MRS metabolic profiles shows that the peritumoral region has a relatively normal profile except for a highly elevated Glu concentration compared with both Gln and Cr. This is in contrast to the tumoral region, where there is a complete reversal of this profile with Gln and Cho being elevated compared with Glu, NAA, and Cr. These data provide further evidence of the dysregulation of the Glu-Gln shuffle, serving as a source of seizures in patients with gliomas. This material was obtained with permission and in collaboration with Andrew Neal and Bradford A. Moffatt at the Melbourne Brain Centre Imaging Unit (MBCIU), the University of Melbourne node of the Australian National Imaging Facility.

Major glutamine pathways in HGGs are featured. Gln undergoes a deamidation to Glu, which subsequently promotes tumorigenic growth either as a substrate in the tricarboxylic acid (TCA) cycle or as a precursor to GSH. The deamidation reaction is catalyzed by glutaminase. This enzyme is the target of glutaminase inhibitors, which may be useful therapeutic agents for patients with gliomas that involve high levels of glutamine detected by 7T MRS. PEP indicates phosphoenolpyruvate.

Exemplary 7T concentric ring trajectory FID-MRSI spectra of a patient with GBM. This method uses FID acquisition combined with concentric ring trajectories, bringing together multiple potential benefits: high resolution and acceleration while maintaining sufficient SNR, low SAR, B₁ insensitivity, no selection box, and detection of J-coupled metabolites with 7T spectral separation. This measurement was acquired in 15 minutes with a nominal isotropic resolution of 3.4 mm, covering the cerebrum. Well-defined metabolic peaks are observed at 3 points: a tCho and Gly hotspot, a tCho and Gly cold spot, and normal-appearing white matter (NAWM). It is noticeable that even in the tumor tCho cold spot, tCho concentrations are higher than in NAWM but about 50% lower than in the tCho hotspot. Two of the metabolites that appear in these plots (Gly and Gln) have emerged as promising therapeutic targets and may serve as imaging biomarkers for patients with HGG. This material was obtained with permission from Gilbert Hangel at the High-field MR Center at the Medical University of Vienna. T1w indicates T1WI; tCr, total Cr.

7T MRSI with standard second order shimming and higher order shimming with an AC/DC shim array was used to visualize Cho and 2HG in an IDH1 astrocytoma. A metabolic hallmark of IDH1 and IDH2 gliomas, 2HG generates a particularly strong signal at 7T, which may make it easier to diagnose patients with IDH-mutant profiles. The SNR of 2HG is lower in this example because this patient was treated with an operation and radiochemotherapy, which decrease 2HG levels. The primary clinical objective in this study was to determine whether there were residual mutant IDH tumor cells posttreatment. The white arrows indicate the frontal area where there are missing voxels in the Cho metabolic map and falsely increased values in the 2HG map due to a larger spectral linewidth obtained with second order shimming. The tumor has a higher contrast-to-noise ratio in the 2HG and Cho maps obtained with the AC/DC shim array. Examples of spectra are shown from tumor and healthy brain in the frontal region (corresponding to the white arrows). The position of the 2HG peak at 2.25 ppm is indicated in all spectra. For the adiabatic spin-echo excitation with TE = 78 ms, a negative peak should be obtained for 2HG, which is clearly visible in the tumor spectrum with AC/DC shim but not apparent in the tumor spectrum with standard second order shimming (2SH) shim. In particular, the frontal spectrum obtained with the 2SH shim is completely destroyed by the B₀ inhomogeneity, while metabolite peaks are clearly visible with the AC/DC shim. 2HG is falsely fit in the frontal healthy spectrum with the 2SH shim due to negative spectral artifacts that appear at the 2.25-ppm 2HG peak position. The dashed vertical line indicates the location of the main 2HG peak at 2.25 ppm, which should be negative at 7T and TE = 78 ms. All the voxels in the MRSI were fit to create a metabolic map. A spectrum from the frontal voxel was chosen to show a false-positive fit of 2HG in healthy brain when the spectral quality is not adequate. Frontal brain regions are difficult to shim with standard methods, and the AC/DC coil can improve B₀ homogeneity due to additional B₀ shimming. Frontal loops in AC/DC are very close to frontal brain areas and create complex B₀ field patterns to shim out the susceptibility induced by air tissue around the frontal sinus. The second order shimming was obtained with the manufacture’s software. This material was obtained with permission from and in collaboration with Jason P. Stockmann and Ovidiu C. Andronesi at the A. A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital and Harvard Medical School. LW indicates linewidth.

T1-weighted contrast-enhanced MR imaging (left) of a patient with a glioma subsequently diagnosed with recurrent tumor (true progression) and the same image with a superimposed map of the Cho/NAA ratio (right) acquired using echo-planar spectroscopic imaging. The map shows a hotspot of the elevated Cho/NAA ratio in a region that does not show contrast uptake on postcontrast T1 MR imaging (red depicts Cho/NAA > 1).