13C MRS in human calf muscles at 7T using a double tuned 4 channel 13C-4 channel 1H transceiver phased array.
Guillaume Donati1, Eulalia Serés Roig1, and Rolf Gruetter1,2

1Laboratory of Functional and Metabolic Imaging, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland, 2Department of Radiology, Universities of Lausanne and Geneva, Lausanne, Geneva, Switzerland

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 C1 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: 88x80mm2, 1H: 120x90mm2) were chosen for efficient B1+ and B1- 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. Sij 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. B1+ and SAR10g,max were measured at 75MHz and 300MHz, with all loops driven in quadrature (0o,90o,180o,270o), 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 C1 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 B1+ 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 B1+ over the 13C array FOV. Energy deposition (fig.3) is mainly localized in subcutaneous regions close to the coil (SAR10g,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 C1 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

Figures

Figure 1: (a) Double tuned 13C-1H transceiver phased array, consisting of a concentric combination of (b) a 4 channel 13C array (∅=23cm, loops size: 88x80mm2) and (c) a 4 channel 1H array (∅=26cm, loops size: 120x90mm2).

Figure 2: Simulated B1+ in the calf muscles transverse plane at 75MHz (top) and 300MHz (bottom). Both arrays were driven in quadrature with 1W total input power.

Figure 3: Simulated local SAR in the calf muscles transverse plane at 75MHz (top) and 300MHz (bottom). Both arrays were driven in quadrature with 1W total input power. The green squares represent the position of the SAR10g,max cubes (1.29[W/kg] at 75MHz and 0.61[W/kg] at 300MHz).

Figure 4: Combined 13C calf muscles spectrum showing 1H-decoupled glycogen resonance from a male subject at 100.5ppm, acquired with the double-tuned 4 channel 13C-4 channel 1H transceiver array coil (vector size=2048, TR=3.4s, BW=8 kHz, acquisition time=256ms, decoupling duration=20ms, 1000 averages). Inset: anatomical transverse 3D GRE image of the calf muscles.



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
3509