Byeong-Yeul Lee1, Xiao-Hong Zhu1, Myung Kyun Woo1, and Wei Chen1
1Center for Magnetic Resonance Research, Department of Radiology, University of Minnesota Medical School, Minneapolis, MN, United States
Synopsis
Functional/metabolic
changes in different brain regions of interest are of importance for better
understanding of the pathophysiological mechanism underlying the human brain
diseases. In this work, we present a novel design of the dual-channel 31P
MRS system for simultaneous measurements of cerebral high-energy phosphate metabolism
from two brain regions of interest by incorporating a new pulse sequence and
two separated RF surface coils with a transistor-transistor logic (TTL) controller. By successfully
implementing this method, we are able to obtain high quality in vivo 31P
MR spectra from both frontal and occipital lobes within the same amount of time
as the traditional method covering one brain region. From an engineering
perspective, this new approach provides a cost-effective solution for in vivo 31P
MRS study of multiple brain regions with a conventional single-channel transmitter-receiver
configuration. Therefore, this valuable MR tool can be used in examining the cerebral
energy metabolism across different brain regions, and
the same approach could be employed to other spin applications.
Introduction
With increasing recognition of
complex neurological disorders with distinct progression in different brain regions,
it is essential to explore functional/metabolic impairments in various brain
regions of interest; for instance, Parkinson’s disease (PD) involves motor dysfunction
in motor cortex as well as non-motor cognitive deficits in the frontal lobe [1].
For this reason, a head volume RF coil has been preferred to cover the entire
human brain despite high cost and a drawback of relatively lower sensitivity
for detecting brain metabolites. As a cost-effective and time-efficient engineering
solution, thus, we designed a novel dual-channel 31P surface coils system
and incorporated that with a new pulse sequence and a transistor-transistor logic (TTL)
controller for simultaneous measurements of energy metabolism from two brain
regions. To test this method, the frontal and occipital lobes were selected for
studying high-energy phosphate metabolism using in vivo 31P MRS in combine with the magnetization
transfer (31P-MT) technique, which offers capability of examining the
key bioenergetic reactions catalyzed by the creatine kinase (CK) and ATPase
enzymes. [2-3]
Methods
All MR experiments
were performed at 7.0T/90cm whole body scanner(Siemens). Each channel targeting
one brain region of interest consists of a butterfly 1H coil for
anatomical imaging and B0 shimming, and a single-loop 31P
coil for 31P MR spectra. The B1 insensitive
selective train to obliterate signal scheme (BISTRO) [4] was applied
to saturate the γ-ATP
resonance followed by a single-pulse-acquire sequence (320 averaging, 3s TR,
5kHz spectral bandwidth (BW), 300 ms hard
pulse with an Ernst flip angle of 84° for excitation). Moreover, 3D chemical
shift imaging (CSI) was acquired using Fourier series window [5] (1.2 s
TR, 5kHz BW, 300 ms hard
excitation pulse, and phase encoding steps 9x9x7, FOV = 120x120x90 mm3). As shown in Fig. 1, 31P MRS data
for each coil were alternatively acquired by switching each channel at the
half TR and each measurement was done within the same apparent acquisition time.
RF transmitter powers for 90-degree excitation pulses were separately
calibrated for each channel for setup of Ernst flip angles. Results and Discussion
Figure 2 shows a general scheme or
pulse sequence of the 31P dual-channel system for the simultaneous
measurement from two targeted brain regions. Using a single transmit amplifier and
receiver channel incorporating with TTL gate function, 31P MRS data were
successfully collected from each channel without doubling the acquisition time.
Figure 3 displays representative in vivo
31P-MT spectra of the human frontal and occipital lobes with and
without γ-ATP
saturation, showing excellent
spectral quality (spectral linewidth of PCr < 11 Hz) and effective MT
saturation efficiency. Notably, with application of additional adjustment of
the linear shim gradients (see Fig. 2), the 31P MR spectrum of the frontal
brain region reached a comparable quality as the occipital lobe, which enables reliable
quantification of cerebral phosphorus metabolites concentration and changes in
both brain regions. In addition, the 3D 31P MRS CSIs shown in Fig. 4
demonstrate the sufficient coverage and good B0 homogeneity of the
dual-coil system that result in excellent spectral quality in both brain
regions.Conclusion
In this work, we demonstrate a novel design of
dual-channel 31P system for simultaneous measurement of the regional
high-energy phosphorous metabolism in the human brains of interest. From an
engineering perspective, the new approach offers a cost-effective and
time-efficient solution for high quality in
vivo
31P
MRS measurements from multiple brain regions using a conventional
single-channel transmitter-receiver configuration. Therefore, this approach
could provide a valuable MR tool for examining the cerebral energy metabolism and
its impairment across different brain regions. The same approach could
be employed to other nuclear spin applications.Acknowledgements
NIH
grants: R01 NS057560, NS070839, MH111447; R24
MH106049, S10RR026783, P41 EB015894, and P30 NS057091; and the AHC Faculty
Research Development (FRD) grant from the University of Minnesota.References
[1] Taylor et al., Brain, 109: 845-883
(1986); [2] Du et al., PNAS, 105: 6409-6414 (2008);
[3] Zhu et al., Neuroimage, 60: 2107-17 (2012);
[4] de Graaf et al., J Magn Reson B, 113: 35-45 (1996);
[5] Hendrich et al, J Magn Reson, 105:225–232 (1994).