Tae Kim1, Yoojin Lee1, Tiejun Zhao2, Hoby P Hetherington1, and Jullie W Pan1
1University of Pittsburgh, Pittsburgh, PA, United States, 2Siemens, Pittsburgh, PA, United States
Synopsis
B0 shimming
is important for gradient echo functional MRI where T2* signal loss and
precession occur from both physiological and non-physiological susceptibility
effects. We used the high degree shim insert (3rd, 4th
and two 5th degree shims) to assess its effect for 2mm isotropic
whole brain GE-EPI BOLD (breath-hold induced) signal at 7T. Comparing 1st-2nd
with high degree shimming, the Δ|B0|
changes are spatially varying. For activation, the largest regions of increase
are in the inferior frontal region; the largest regions of decrease are in the
middle temporal lobe. Overall, there is a 4.3% increase in total activated
pixels.
Purpose
The improvement of B0 shimming is important for
gradient echo functional MRI where T2* signal loss and precession occur from
both physiological and non-physiological susceptibility effects, these effects
being substantially worse at 7T and with echo-planar imaging where pixel shift
produces complex signal distortion. As a result, there has been much effort on
methods to improve GE fMRI. Here we describe the quantitative improvement in whole
brain BOLD signal and activated pixel counts using high degree spherical
harmonic shimming. Methods
B0
shim insert, field
map and shimming: A
shim insert coil consisting of 3rd,
4th degree and two 5th degree shims (ZC4, ZS4)
with 10A shim supplies (RRI, Billerica, MA) was used for high degree shimming,
denoted as 1st-4th+ shimming. The B0 field was mapped using the B0 loop encoded readout (Bolero) method,
with shimming performed by a least squares optimization based on a calibrated
spherical harmonic model with a user-determined target ROI shown in Fig. 1A. To
analyze EPI data, all pixels were binned in 10Hz increments according to change
in |B0| offset between 1st
– 2nd and 1st – 4th+ shims, i.e., ΔB0=|B01,2| - |B01-4+| (improved
homogeneity pixels with 1st-4th+ compared to 1st-2nd
shim are in positive bins; deteriorated pixels in negative bins).
RF coil: An
8x2 (two rows, eight coils/row) inductively decoupled elliptical transceiver
array was used in parallel transmit mode. RF shimming per subject was performed
with eight 1kW transmit channels which were split and phased to generate a
circularly polarized mode-like distribution. The achieved B1+ was 460±51Hz over the entire head at
1140±113 Watts total applied power.
EPI
and breath hold BOLD activation: Single-shot GE-EPI
2mm3 (48 slices, matrix size=96´96, bandwidth/pixel=13.88Hz, echospacing 750ms)
was acquired in 6 volunteers; FOV=19.2x19.2cm2, TR=3.5s, TE=24ms, phase
partial Fourier=6/8, FA=60°.
For the whole brain BOLD signal response, a 21-sec breath-hold protocol was
performed five times using a block-design paradigm (140s − [21s (breath hold)
−35s] x5). N=8 subjects were asked to exhale prior to breath-holding to
preclude a biphasic change (1). Each run
was acquired with 1st-2nd and 1st-4th+
degree shimming and signal averaged in randomized order. Processing was
performed using AFNI (http://afni.nimh.nih.gov/afni/),
FSL (http://fsl.fmrib.ox.ac.uk/fsl/fslwiki/)
and SPM (http://www.fil.ion.ucl.ac.uk/spm/)
programs combined with in-house programs written in Matlab R2013b. The Bolero B0 map was used to calculate
inhomogeneity induced voxel displacements. Following normalization by the mean
signal intensity at each voxel, BOLD maps were estimated by linear regression
using AFNI (3dDeconvolve), which also included motion parameters. The significance
of activation was determined on a pixel-by-pixel basis over each DB0
bin(p-value<0.05). MP2RAGE
images were used for anatomical registration using (0.75 mm)3
resolution with TR=6s, TE=3.1ms, TI=0.8/2.7s, and GRAPPA 3. All studies were
approved per the University of Pittsburgh IRB.Results
The ΔB0 bins,
as presented in Talairach space from n=8 volunteers
(Fig. 1B) shows that the high degree shimming had its greatest effects over the
inferior frontal and temporal regions. For both the positive and negative bins,
the BOLD % signal change is significant, being increased in the positive bins
and decreased in the negative bins. In both
positive and negative bins, there are significant changes in numbers of
activated pixels. From n=8 volunteers, Fig. 2A shows that the
high degree shimming significantly increased the numbers of activated pixels in
the positive Δ|B0| bins,
particularly above +40Hz, while they decreased in the negative bins. For all bins, the activated pixel numbers (green)
were significantly different between 1st-2nd and 1st-4th+
shims. For most of the bins, the BOLD %signal change (orange) was
significantly different (p<0.05) between the 1st-2nd
and 1st-4th+ shims; Fig. 2B shows the locations and
fractional change in activated pixel numbers and BOLD % signal change averaged
over the 8 volunteers shown in Talairach space. Data from a single subject is
shown in Fig. 2C.Discussion
As an independent means of improving
field homogeneity, high degree shimming does not interact with other imaging
parameters and is compatible with whole brain coverage necessary for
simultaneous multi-slice methods. Comparing 1st-2nd and 1st-4th+
shimming, the Δ|B0|
changes spatially vary over the brain with the majority of the brain either
maintaining or increasing signal intensity and activation. Focusing on the
pixels that substantially change (either improved or worsened, outside of the
two center Δ|B0| bins)
with the 1st-4th+ shimming, for each 1 activated pixel
that is lost, there are 7.9 activated pixels gained. The largest regions of
activation increase are seen in the inferior frontal region while the largest
regions of activation decrease are in the middle temporal lobe. Overall, there
is a 4.3% increase in total activated pixels.Acknowledgements
This work is supported by NIH R01EB011639; R01NS081772;
R01NS090417; R01EB009871 and RSNA RSCH1314.References
1. Li TQ, Kastrup A,
Takahashi AM, Moseley ME. Functional MRI of human brain during breath holding
by BOLD and FAIR techniques. Neuroimage 1999;9(2):243-249.