Xiaoping Wu1, Edward J. Auerbach1, An T. Vu2, Steen Moeller1, Keith Jamison1, Sebastian Schmitter1,3, Pierre-Francois Van de Moortele1, Essa Yacoub1, and Kamil Ugurbil1
1Radiology, University of Minnesota, Minneapolis, MN, United States, 2Center for Imaging of Neurodegenerative Diseases, VA Healthcare System, San Francisco, CA, United States, 3Physikalisch-Technische Bundesanstalt, Berlin, Germany
Synopsis
A major component of the Human Connectome Project (HCP) in the WU-Minn
consortium is multiband-accelerated whole-brain resting-state functional MRI (rfMRI)
at both 3T and 7T. Although providing better contrast and higher spatial resolutions,
the 7T acquisition is compromised by RF nonuniformity. Here, we demonstrate the
utility of RF parallel transmission (pTx) for 7T HCP-type rfMRI with 1.6-mm isotropic
resolutions. Our results show that pTx can significantly enhance temporal SNR
across the entire cortical surfaces and in many subcortical voxels relative to a
CP-like-mode RF shimming mimicking single-transmit configurations, thereby
holding great potential for acquiring high-quality, high-resolution and high-efficiency
rfMRI data.
Purpose
To investigate how RF parallel transmission (pTx) can be used to improve
the blood-oxygenation-level-dependent (BOLD) contrast when acquiring Human
Connectome Project (HCP)-type whole-brain resting-state functional MRI (fMRI) at
7 Tesla (7T) with 1.6-mm isotropic resolution. Methods
We conducted human
studies on a 7T MR scanner (Siemens, Erlangen, Germany), equipped with
a prototype pTx system allowing for up to 16 transmit RF channels. Healthy
subjects who signed a consent form were scanned using the Nova 8 transmit 32
receive (8Tx/32Rx) head coil (Nova Medical, Inc., MA, USA). The coil was used
in the “protected” mode to ensure RF safety. Additionally, band-specific pTx multiband
(MB) pulses with single spokes (i.e., RF shimming) were designed
using the slab-wise design framework 1. To capitalize on coil geometry and promote RF
performance, pulses were designed to image sagittal slices 2. Based on the MB sequence used in the HCP, a new
pTx-enabled, 2D gradient-echo echo-planar-imaging (EPI) sequence suitable for BOLD fMRI acquisitions
was developed to enable application of multiple pTx MB RF pulses for
excitation. We acquired whole-brain resting-state fMRI (rfMRI) data with 1.6-mm
isotropic resolutions and 5-fold slice acceleration (MB5) with inverted phase-encode directions (anterior-posterior (AP) and posterior-anterior (PA)) as in the 7T HCP rfMRI
protocol 3. In each phase-encode acquisition, a time series of 900 image volumes was
acquired, yielding a total of 1800 volumes in total scan time of 33 minutes;
this is less than the 1-hour acquisition in the HCP but sufficiently long for
proof of principle demonstration. During the data acquisition, the subject was
instructed to fixate at a black cross displayed over a white background.
For comparison, we also mimicked a single-transmit configuration by performing
RF phase shimming targeting a Circularly Polarized (CP)-like-mode 4 RF distribution within the brain, and utilized
this shimming to acquire rfMRI data with same imaging parameters as in pTx
acquisition. To demonstrate the benefit of pTx, temporal signal-to-noise ratios
(tSNR) were calculated after the rfMRI data underwent the HCP spatial 5 and temporal 6 preprocessing pipelines and were compared. As
required by the HCP preprocessing pipelines, high-resolution whole-brain T1-weighted
and T2-weighted structural images were acquired, both with 0.7-mm
isotropic resolution and using the CP-like-mode RF pulses. The T1-weighted image was acquired
prior to the rfMRI data acquisition and was also used to derive a brain mask
defining the region of interest for the subsequent pTx pulse design. All pulse
designs were performed in Matlab (Mathworks, USA).Results
The use of pTx substantially improved RF uniformity across the brain relative to the CP-like-mode counterpart (Fig. 1). Despite of the non-uniform RF distribution across the brain, satisfactory definitions of pial and white surfaces
were achieved in most cortical regions when using the CP-like-mode RF shimming
for the structural acquisitions (Fig. 2). After undergoing the HCP
preprocessing pipelines, the rfMRI data presented little residual distortion or
signal dropout (Fig. 3). The improvement in RF uniformity with pTx translated
into enhanced BOLD contrast with increased tSNR observed across the entire
cortical surface and in many subcortical voxels (Fig. 4). Additionally, the use
of pTx resulted in ~36% less RF power delivery (measured as sum of forward
minus reflected power across all transmit channels).Discussion
Our results show
that pTx can be used to improve the BOLD contrast for 7T HCP-type whole-brain rfMRI
with 1.6-mm isotropic resolution while reducing RF power deposition or SAR relative
to the CP-like mode RF shimming. The SAR reduction could potentially be traded
off for higher slice acceleration (e.g., MB6), to increase data for constant scan
time, which is highly desirable for rfMRI data analyses. Our next immediate
step is to acquire data for a total scan time of ~1 hour as in the 7T HCP rfMRI
protocol and compare pTx data to those obtained with the Nova 1Tx32Rx head coil
with dielectric padding as in the HCP. Future work will examine rfMRI
with faster volumetric acquisition (i.e. use of higher MB factors), and integrate
pTx into structural acquisitions to improve image quality 7,8.Conclusion
We have demonstrated the advantages of pTx over the CP-like-mode RF
phase shimming mimicking single-transmit situations when acquiring HCP-type slice-accelerated
high-resolution whole-brain rfMRI at 7T. Our data suggest that pTx can be used to enhance
BOLD contrast across the entire cortical surfaces and in many subcortical
voxels while reducing SAR, thereby providing an attractive means of acquiring high-quality,
high-resolution and high-efficiency truly
whole-brain rfMRI data that are desired in many neuroscience and clinical
applications.Acknowledgements
The authors would like to thank Brian Hanna for setting up computation
resources. This work was supported by NIH grants including P41 EB015894 and P30
NS076408. References
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