Kun Lu1, Javier Gonzalez-Castillo 2, Matthew Middione3, Brice Fernandez4, Valur Olafsson5, Prantik Kundu6, Ajit Shankaranarayanan7, and Thomas Liu1
1Center for Functional Magnetic Resonance Imaging, University of California, San Diego, La Jolla, CA, United States, 2Laboratory of Brain and Cognition, Section on Functional Imaging Methods, National Institutes of Health, Bethesda, MD, United States, 3Applied Sciences Laboratory West, GE Healthcare, Menlo Park, CA, United States, 4Applications and Workflow, GE Healthcare, Munich, Germany, 5Neuroscience Imaging Center, University of Pittsburgh, Pittsburgh, PA, United States, 6Brain Imaging Center, Icahn Institute of Medicine at Mt. Sinai, New York, NY, United States, 7Applications and Workflow, GE Healthcare, Menlo Park, CA, United States
Synopsis
We recently
observed differences in slow signal drift between multiple echoes in multiband multiecho
EPI data. Such differences in drift compromise
the TE dependence model and could impact the TE dependence analysis (e.g Multiecho Independent Component Analysis ME-ICA).
We first designed a metric MEQA to quantitatively measure the observed drift
differences, then investigated the effects of the drift differences on ME-ICA
analysis.Introduction
Multiband Multiecho (MBME) EPI has the advantage of
higher temporal resolution and improved sensitivity to BOLD signal compared to
conventional single band single echo EPI. A few studies have examined the
benefits of MBME in resting state and task fMRI [1,2]. It has also been
demonstrated that TE-dependent analysis methods (e.g Multiecho Independent
Component Analysis ME-ICA [3]) can be applied to MBME data to effectively remove
non-BOLD signals [1]. However, we recently
observed differences in the slow signal drift between multiple echoes in MBME
data, which could compromise the TE-dependence model and impact the ME-ICA
analysis. Figure 1C. shows an example of such drift differences in an MBME data
acquired on an agar phantom. For better
illustration, we show data from an acquisition with a significant amount of
aliasing artifact in the reconstructed images (Figure 1A). We have noted that areas of aliasing
artifacts often exhibit large drift differences. Our goal is to design a metric
to quantify the differences in drift among multiple echoes, and to probe the
effects of the drift differences on TE dependent analysis such as ME-ICA.
Method
The
previous MBME studies have used in-plane acceleration for faster data
acquisition and reduced off resonance effects.
Gomez et al [4] also indicated that in-plane acceleration combined with
lower multiband factor (2 or 3) increases BOLD temporal SNR. In this study, we acquired both phantom and
in-vivo MBME data with and without in-plane acceleration (Auto-calibrating
Reconstruction for Cartesian Imaging: ARC)
so we can compare the effects of in-plane acceleration on the signal
drift. We used a GE 3T Discovery MR750
(GE Healthcare, Waukesha, WI) and a prototype MBME pulse sequence with blipped
CAIPI [5]. The parameters were: MB=3, 250 time points, 3 echoes, 24cm FOV, and 3.75x3.75x3.8mm
voxel size. For data without ARC: TR = 1.2s, TE = 11, 32.2, and 53.4ms; and
with ARC=2: TR = 1s, TE = 11, 25, and 39ms.
An offline Matlab recon was used for image reconstruction. To quantify the drift differences, we first
performed a fit of the MBME data to obtain T2* and S0 time courses (Figure 2).
The residual time course from this fit was then modeled voxel-wise as a 10th
order Legendre polynomial to remove high frequency noise components that did
not contribute to slow drifts. From this fitted residual, we calculated the
standard deviation and used it as a quantitative measure of the drift difference
(dubbed as MEQA, Figure 2.) For the in-vivo
data, we also performed ME-ICA analysis.
Results
Figure 1B shows an example of the MEQA map. High MEQA values correspond well to voxels
with remaining aliasing artifacts and large echo drift differences. Figure 3 shows calculated MEQA maps from the
MBME phantom and in-vivo data. The data
with in-plane acceleration (ARC=2) has significantly more MEQA voxels than the
data without ARC, indicating more prevalent deviation from the TE dependence model
in the ARC=2 data. This is true for both
the phantom and in-vivo data.
The ME-ICA
analysis shows that the data acquired without ARC has higher number of both
total ICA components and BOLD-like components than the data with ARC (Table 1.)
Discussion
Our results
show that the MEQA metric is a sensitive measure of slow drift differences among multiple echoes in MBME data. Such
differences are typically observed in voxels with imaging artifacts due to
imperfect image reconstruction, susceptibility, and motion (not shown). Therefore
MEQA could potentially be used as a quality assurance metric for MBME data. We also show that data with higher MEQA voxel
counts, and thus more prevalent echo drift differences, has lower ME-ICA
performance. Although very preliminary, this result warrants further
investigations of the source of the drift differences and how they affect ME-ICA
analysis.
Acknowledgements
This work was supported in part by a research grant from
GE Healthcare. References
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