Rebecca Emily Feldman1, Hadrien A Dyvorne1, Rafael O'Halloran1, and Priti Balchandani1
1Translational and Molecular Imaging Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States
Synopsis
The
higher signal-to-noise-ratio offered at 7T, has been shown to increase the resolution
of diffusion MRI as well as the precision and directional certainty of
diffusion-based parameters. Two major drawbacks of 7T dMRI include lengthy
acquisitions and signal loss due to B1-inhomogeneity. SMS methods
reduce the duration of the acquisition, the refocusing pulses typically used in
dMRI are particularly sensitive to B1 non-uniformities leading to a
loss in signal, or even complete signal dropout in parts of the image. We have
created a dMRI sequence with SEAMS PINS and an EPI readout that provides
improved immunity to B1-inhomogeneity. Introduction
The higher signal-to-noise-ratio (SNR) offered at ultra-high magnetic
field strengths, such as 7 Tesla (7T), has been shown to increase the resolution
of diffusion MRI (dMRI) as well as the precision and directional certainty of
diffusion-based parameters [1,2] However, two major drawbacks of 7T dMRI
include lengthy acquisition times and signal loss due to increased inhomogeneity in the applied
radiofrequency (RF) field (B1).
Simultaneous multi-slice (SMS) imaging using multiband excitation and
parallel imaging is becoming more common for accelerating full brain
acquisitions [3]. While SMS reduces the duration of the acquisition, the refocusing
pulses typically used in dMRI are particularly sensitive to B1 non-uniformities
leading to a loss in signal, or even complete signal dropout in parts of the
image. SEmi-Adiabatic Matched-phase Spin-echo (SEAMS) Power Independent of the
Number of Slices (PINS) is an SMS technique that can accelerate imaging while
reducing a spin-echo based sequence's sensitivity to B1 non-uniformities
[4] . We have created a dMRI sequence
with SEAMS PINS excitation and refocusing and an EPI readout that provides
improved immunity to B1-inhomogeneity with RF power deposition, as
measured by the specific absorption rate (SAR), comparable to existing
sequences.
Methods
We created a SEAMS PINS pulse-pair with an excitation pulse duration of
21 ms and a refocusing pulse duration of 14 ms (Figure 1). The pulse-pair was
created to match a refocusing pulse with a bandwidth of 1.11 kHz sampled by 94
lobes, creating a slice separation/slice thickness ratio of 12. The pulse-pair
was inserted into a dMRI sequence with an EPI readout (Figure 2), and EPI
navigators acquired pre-scan [2]. Diffusion-weighted images were acquired using
2 diffusion sequences 1) the SEAMS PINS
pulse-pair and 2) a standard non-adiabatic single-refocused SMS diffusion
pulse-pair with a time-shifted RF pulse multiband factor of 2 [5]. Imaging was
performed in a spherical water phantom on a 7T whole body MRI system (Siemens,
Erlangen). The acquisition was made with: b = 1500 s/mm
2; TE = 73
ms; FOV = 21 cm x 21 cm; matrix = 210 x 210; Time = 9 minutes. Each sequence was
acquired at four power settings, at adiabatic threshold or with the power
calibrated to produce the expected flip angle at the center of the magnet (P
thresh),
at 1.2 x P
thresh, 1.4 x P
thresh, and 1.6 x P
thresh.
Discussion/Results
The SAR ratio for each sequence was noted, although none of the
sequences exceeded the SAR limits for the scanner. The SEAMS PINS diffusion
pulse deposited 80% of the power of the time-shifted sequence, for the same TR
and scan times. The B1-insensitivity
of the sequence is shown in Figure 3. For a central slice of the phantom
(Figure 3A), b = 1500 s/mm2, the signal received on a projection
through the phantom (Fig. 3A white line) is plotted for each power setting for
both sequences. The signal produced by the non-adiabatic SMS diffusion sequence
shows high sensitivity to B1 across the initial projection through
the phantom. As the transmit B1 increases by 20%, most of the signal
in the center of the phantom is destroyed, and as the B1 continues
to increase, a larger region of the phantom experiences complete dropout. In
contrast to this, the signal produced by the SEAMS PINS pulse-pair, is more
consistent across the body of the phantom. It shows much less variation over the
phantom cross-section as the power is increased by 20%, and even at 1.6 x
adiabatic threshold, no portion of the phantom experiences complete signal
dropout.
At ultra-high fields, dMRI using SEAMS PINS can achieve accelerated simultaneous multi-slice imaging while restoring diffusion-weighted signal to regions that would experience excessive signal dropout using non-adiabatic pulse-pairs. The sequence is substantially more robust to B1 inhomogeneity, while maintaining SAR deposition levels similar to those of existing non-adiabatic sequences. Future work involves further reduction of minimum achievable echo time and validation of the sequence in vivo.
Acknowledgements
NIH-NINDS R00
NS070821. Thanks to Dr. Junqian (Gordon) Xu for helpful
discussions.References
[1] Polders DL et al 2011 MRM 33:1456-63 [2] Dyvorne et al MRM (epub)
June 2015 [3] Eichner et al 2014 MRM
72:949-58 [4] Feldman et al MRM (epub) March 2015 [5] Auerbach et al 2013
69:1261-7