Synopsis
The inherent low sensitivity of 13C MRS makes direct 13C detection
challenging. Moreover, the 13C-1H heteronuclear J coupling requires double tuned
13C-1H coils to perform proton decoupling during 13C signal acquisition. High
sensitivity can be achieved over a large field-of-view using array coils. We
aimed to design and build a 4 channel 13C-4 channel 1H transceiver phased-array
coil for 13C-MRS studies in humans at ultra-high field. Electromagnetic performance
of the coil was evaluated by FDTD simulations in calf muscles at both
frequencies. Finally, 1H-decoupled 13C resonance of Glycogen C1 was successfully
detected in volunteer calf muscles at 7T.
Introduction
13C MRS is a powerful tool for non-invasive investigation
of carbohydrate metabolism, such as natural abundance glycogen in human muscle [1].
In terms of RF-coil design, inherent low sensitivity of
13C signals
and heteronuclear
13C-
1H
J coupling require double tuned
13C-
1H coils
to provide high sensitivity at the
13C frequency [2,3]. Moreover,
high transmit efficiency at
1H frequency is needed to ensure proper
1H
decoupling during
13C signal acquisition. Double tuned transceiver
array with extended spatial coverage were recently designed for X-nucleus
spectroscopy [4,5]. We aimed to demonstrate that a 4 channel
13C-4
channel
1H array coil can be successfully used for
in vivo 13C MRS studies in
humans at ultra-high field. Coil performance was evaluated by detecting
in vivo 1H-decoupled
13C resonance
of Glycogen C
1 in calf muscles at 7T.
Methods
Coil design: A double tuned 4 channel
13C-4 channel
1H transceiver
phased array coil (fig.1) was designed, built and optimized for human studies at
7T [5]. Its dimensions allow MR-measurements in different body part, such as
calf muscles or brain. The loop dimensions (
13C: 88x80mm
2,
1H:
120x90mm
2) were chosen for efficient B
1+ and B
1-
at
13C frequency (75MHz) and for high transmit efficiency at
1H
frequency (300MHz). The coil FOV can cover either the back half of the brain or
both calf muscles.
Bench measurements: Bench measurements were performed using a Network-Analyzer (E5071C;
Agilent, USA). The coil, loaded with two calf muscles of a male volunteer, was
matched at 50Ω. S
ij
parameters, unloaded and loaded quality factors were measured at 75MHz and 300MHz.
Simulations: FDTD
simulations were performed using Sim4Life (ZMT, Switzerland) on the posable Duke
model from “Virtual Family” (ITIS, Switzerland). Legs were placed next to each
other in order to load the coil with the two calf muscles. B
1+
and SAR
10g,max were measured at 75MHz and 300MHz, with all loops
driven in quadrature (0
o,90
o,180
o,270
o),
for 1W total input power.
MR measurements: MR experiments were performed
on a 7T human scanner (Siemens, Erlangen, Germany). Natural abundance
13C
spectra were acquired on a healthy male volunteer (age=26y, weight=82kg) who
gave informed consent according to the procedure approved by the local ethics
committee. Coil’s FOV covered both calf muscles of the volunteer in supine
position. Glycogen C
1 resonance was acquired using an adiabatic
half passage (AHP) pulse for excitation (2ms) and continuous wave (CW) for
1H
decoupling during
13C signal acquisition (vector size=2048, TR=3.4s,
BW=8 kHz, acquisition time=256ms, decoupling duration=20ms, 1000 averages). Spectra
acquired by each loop were combined to further enhance the SNR.
Results
Bench measurements: Reflected power of individual loops was lower than -25dB. Isolation
between the loops was better than -12dB for the
13C array and -15dB
for the
1H array. The cross-coupling between
1H and
13C
loops was lower than -20dB at 75MHz and 300MHz. The unloaded to loaded Q-ratio
was ~350/90 for the
13C loops and ~280/100 for the
1H
loops, demonstrating good coil efficiency.
Simulations: The B
1+
produced by the
13C array in quadrature mode exhibits a large and
symmetric spatial coverage on both calf muscles (fig.2). With 1W total input
power, it can reach up to 8µT in regions close to the loops, and around 3µT at
3cm depth. With the same input parameters, the
1H array generates an
almost symmetric B
1+ over the
13C array FOV. Energy
deposition (fig.3) is mainly localized in subcutaneous regions close to the coil (SAR
10g,max=1.29[W/kg]
at 75MHz and 0.61[W/kg] at 300MHz).
MR
measurements: Glycogen
C1 from the gastrocnemius muscles of the human calves was detected at 100.5ppm, as well as lipids
from subcutaneous adipose tissue, such as glycerol at 62ppm and 69.5ppm and
unsaturated lipid at 130ppm, indicating high sensitivity of the
13C
array coil. Moreover, the glycogen C
1 resonance was successfully
decoupled, as suggested by the
in vivo
13C spectrum (fig.4), indicating a good transmit efficiency of the
1H
array coil within the sensitive volume of the
13C array coil.
Conclusion
It is feasible to perform
in vivo 1H-decoupled
13C MRS in the human calves
at 7T using double tuned
13C-
1H transceiver array coils. The
4 channel
13C-4 channel
1H array coil presented in this
work provides larger FOV than single loop surface coils, while exhibiting a
strong sensitivity at the
13C frequency and high transmit efficiency
at the
1H frequency. These results confirm the potential of array
coils to perform further
13C MRS in humans at ultra-high field,
especially in the brain, where the metabolite concentrations are even lower.
Acknowledgements
Supported by Centre d’Imagerie BioMédicale
(CIBM) of the UNIL, UNIGE, HUG, CHUV, EPFL and the Leenaards and Jeantet
Foundations.References
[1] M.J. Avison et al, 1988; [2] G. Adriany et al, 1997; [3] E. Serés Roig et al, 2014; [4] N.I. Avdievich, 2011; [5] G. Donati et al, ISMRM 2015