Jabrane Karkouri *1, Mary McLean *2, Minghao Zhang *1, Joshua D Kaggie2, Ashley Grimmer2, Alixander Khan2, Tomasz Matys2, Daniel Atkinson1, Ferdia Gallagher *2, and Christopher Rodgers *1
1University of Cambridge, Cambridge, United Kingdom, 2Radiology, University of Cambridge, Cambridge, United Kingdom
Synopsis
Keywords: Deuterium, Deuterium
Deuterium metabolic imaging (DMI) is a new method to probe
brain metabolism. Theory predicts higher SNR at higher field strength, but
clinical translation is easier at lower field strength. We undertook
2H
MRSI in 3 healthy volunteers at 3T and 7T sequentially. Acquisition was
undertaken at baseline and after 11.1g oral D2O consumption. Data
quality was acceptable in all scans. SNR was 3x higher at 7T, in agreement with theory.
D
2O cerebral uptake rate was similar between field strengths (0.13 min-1
at 3T vs 0.07 min-1 at 7T).
Introduction
Deuterium metabolic imaging (DMI) is an emerging method to probe
metabolism in vivo. The technique has been
investigated at 3T [Kaggie et al, 2022, Niess et. al., 2022], 4T [De Feyter,
et. al., 2018], 7T [De Graaf et. al., 2019], and 9.4T [Ruhm et. al., 2021]. MRI
physics predicts enhanced signal-to-noise from systems operating at ultra-high
field which would motivate using high field strengths to scan. Yet the
availability of ultra-high field MRI systems is limited with only around 100
systems globally compared to approximately 30,000 3T MRI systems. It is
important to understand in practical terms whether 3T is sufficient for human
in vivo DMI. We report results from a direct sequential comparison of 2H MRSI scans run at 3T and 7T in phantoms and healthy volunteers
using volume head coils [Peronnet et al. 2012].Methods
Data were
acquired using a 3T Signa MRI (MR750, Ge Healthcare, USA) quadrature volume 2H
transmit-receive head coil built locally [Kaggie et al, 2022] and a 7T Terra MRI (Siemens) with a 2H/1H
head coil comprising 2x 1H transmit-receive channels, 2x 2H
transmit-receive channels forming a TEM resonator and 16x 2H receive
loops (Virtumed LLC, MN, USA).
Phantom
scans were performed on a cylindrical phantom containing agar jelly and water with
2% deuterium enrichment (Figure 2). NaCl was added for a conductivity of 1.0
S/m and Dotarem was added to yield T1 of
1100 ms for 1H at 7 T and 360 ms for 2H.
Three healthy
volunteers (3 males, age 25-31 years, BMI 21.5-22.8 kg/m2) gave
written consent and were scanned using the protocol in Figure 1. Briefly,
baseline scans (i.e. without deuterium enrichment) were made at one scanner.
Then the subject drank 11.1 g D2O diluted with 240 mL potable water
before a second follow up on the same scanner. The subject then walked to the
second scanner for their third scan taking ~5 min. The starting field strength was
alternated.
Measurements
at baseline and after the administration of D2O consisted of localizers,
B0-maps and non-localized 2H FIDs and localized acquisition
weighted 3D CSI (Figure 1).
Data were
loaded into Matlab using our OXSA [Purvis. et. al., 2017] toolbox for 7T data and GE data reading scripts
provided by Rolf Schulte (General Electric) for 3T data. Raw k-space data were
Hamming filtered, zero padded and Fourier transformed to image space. The
single-channel 7T results were combined using WSVD. Spectra were fitted with
AMARES in OXSA.
Results are compared in terms of the signal-to-noise ratio
(defined as the ratio of max signal amplitude by the standard deviation of the noise from a frequency region without any
signal), linewidth, and quantitative HDO concentration after calibration to the
natural abundance baseline scan . Results
Figure 2 shows the phantom results of the CSI acquisitions
performed on the 2 sites.
Figure 3 shows the in vivo non localized FID results comparison
between before and after D2O administration and between sites.
Figure 4 is an illustration of the D2O time course for
all 3 volunteers that have participated to this study.
Figure 5 shows the D2O concentration time course based
on literature values [Kaggie et. al., 2022].Discussion & Conclusion
Both 3T and 7T scanners at our site can detect HDO signals
after ingestion of 11.1g D2O. Linewidths in Hz are comparable, meaning
that metabolites detected in a scan with 6,6’-[2H2]-glucose
will be approximately 2.3x better separated at 7T compared to 3T.
The signal uniformity is different between the 2 sites
because of the different coil designs. Indeed, at 7T, the head coil has
transmitters at the bottom of the coil and the back of the head lies closely on the receivers loops.
The ratio of post/pre signal appears stronger at 3T than at
7T.
These figures will aid the comparison of DMI between field
strengths.
Acknowledgements
Jabrane Karkouri was supported by the
EU Horizon 2020 program under grant agreement #801075 “NICI” and by Innovate UK
(10032205) under the Guarantee Scheme relating to the EU Horizon Europe project
MITI (101058229). This research was supported by the NIHR Cambridge Biomedical
Research Centre (BRC-1215-20014). The views expressed are those of the
author(s) and not necessarily those of the NIHR or the Department of Health and
Social Care. We
acknowledge support from Cancer Research UK, The Cambridge Experimental Cancer
Medicine Centre, the CRUK Cambridge Centre, NIHR Cambridge BRC, NIHR Cambridge
Clinical Research Facility, Addenbrooke’s Charitable Trust, the Evelyn Trust,
and the MS Society. Minghao Zhang is supported by the Medical Research Council (MR N013433-1) and the Cambridge Trust. References
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