Afonso Dias1, Marta Bianciardi2, Sandro Daniel Nunes1, Luís M. Silveira3, Lawrence L. Wald2, and Patrícia Figueiredo1
1ISR-Lisboa/LARSyS and Department of Bioengineering, Instituto Superior Técnico – Universidade de Lisboa, Lisbon, Portugal, 2Department of Radiology, A.A. Martinos Center for Biomedical Imaging, MGH and Harvard Medical School, Boston, MA, United States, 3INESC-ID, Instituto Superior Técnico – Universidade de Lisboa, Lisbon, Portugal
Synopsis
We
propose a new metric of local
functional connectivity for the parcellation of the cerebral cortex from
resting-state fMRI data. It is based on the hypothesis that the anisotropy of
the local spatio-temporal correlation tensor of the BOLD signal is increased in
the boundaries between regions of functional segregation within gray matter. We
show that the anisotropy of rs-fMRI at 7T can be used to generate cortical
parcellations that are partially consistent with the results obtained using the
well-established stability map. Further
work is needed to investigate the validity and properties of the parcellations
based on the proposed metric.Introduction
Parcellation of the cerebral cortex into
functionally meaningful regions is a crucial step in studies of brain function using
complex network analysis. Local functional connectivity (LFC) metrics play a
key role in methods of cortical parcellation based on resting-state fMRI (rs-fMRI),
by revealing patterns of correlated BOLD signal variation and hence allowing the
identification of contiguous but functionally segregated regions [1]. Recently,
a new method for analyzing rs-fMRI data by means of a local spatio-temporal
correlation tensor was proposed [2]. Their work largely focused on the presence
of anisotropic correlations in the white matter. However, they also conjectured
that these tensors should be mostly isotropic in grey matter, with the
exception of boundaries between regions of functional segregation. Here, we investigate
the validity of this hypothesis by studying the suitability of correlational
anisotropy maps (AM) calculated from rs-fMRI data collected at 7T to provide
functional structure information for cortical parcellation. We employ a hierarchical
parcellation method that we have previously proposed, and compare the results
with the originally used metric, the stability map (SM) [3].
Methods
Data acquisition and
pre-processing
Data from one healthy
subject collected on a 7T whole-body scanner with a 32-channel-receive RF coil
was used to test the proposed methodology. 2x5min of rs-fMRI data were
collected using a GE-EPI sequence with TE=32ms, TR=2.5s, FA=75º, GRAPPA factor
= 3, simultaneous-multi-slice factor = 3, nominal echo spacing = 0.82ms,
whole-brain coverage by 123 sagittal slices and 1.1mm isotropic
resolution. A T1-weighted structural image was also acquired using
multi-echo MPRAGE, with 1mm isotropic resolution3. Data analysis was
carried out using Matlab, FSL and Freesurfer tools.
Pre-processing
of rs-fMRI data included: motion correction; slice time correction;
physiological noise correction using an extended RETROICOR based on
simultaneous cardiac and respiratory data4; minimal spatial
smoothing with a 1.5mm FWHM Gaussian kernel; and normalisation by removal of
the temporal mean and re-scaling to unit variance. The structural image was co-registered
with fMRI and MNI images, and it was subjected to tissue segmentation and
cortical surface reconstruction using Freesurfer.
Anisotropy map
A local spatio-temporal correlation tensor is
computed for every voxel according to [2], while using an additional constraint
to ensure that the resulting symmetric 3x3 matrix representing the tensor
remains positive semi-definite. The correlational anisotropy map (AM) is then
obtained by computing the fractional anisotropy from each tensor according to [5].
For comparison, a stability map (SM) is also computed as in [1,3].
Cortical parcellation
The hierarchical brain parcellation method based
on discrete Morse theory proposed in our previous work [3] was chosen for its ability
to deal with different scales and for its high intra-subject reproducibility,
as these properties could be beneficial in evaluating the role of this new
metric. We model the AM projected on the cortical surface as a simplicial
complex. This allows us to apply this parcellation method as it generalizes to
any regular cell complex of dimension 3 or less with a function defined on its
vertices [6]. Parcellations are performed using both the AM and SM, for a
number of persistence thresholds.
Results
The
cortical parcellations obtained using the two metrics, AM and SM, for
persistence threshold of approximately 0.4 are shown in Fig.1. Despite obvious
differences, the two parcellations exhibit some matching features, which are
highlighted by the contours. Some parcels are almost exactly matched (red,
orange, blue, purple). In other cases, an SM-derived parcel closely
matches the reunion of a number of AM-derived parcels (green, yellow).
The number of parcels obtained as a function of
persistence threshold is shown in Fig.2; it is systematically higher when using
the AM compared to the SM, and also increases more rapidly as the persistence
is decreased. Although this finding could suggest that anisotropy provides
additional detail or structure, it is also possible that it reflects a higher
noise level.
Conclusion
We show that the anisotropy of local
spatio-temporal correlation of rs-fMRI at 7T can be used as an LFC metric to generate
functional parcellations of the cerebral cortex, which are partially consistent
with the results obtained using an established LFC metric, the stability map. The
differences encountered in the parcellations obtained by using the two LFC
metrics suggest that the correlational anisotropy may provide additional structure relative to the stability map, or instead
noisier information. Future work will be aimed at further investigating the
validity and properties of the parcellations based on the proposed anisotropy
metric, through the analysis of an extended dataset, the exploration of
different spatial smoothing levels, and a systematic comparison with
well-established techniques.
Acknowledgements
This work was funded by FCT grants
PTDC/EEI-ELC/3246/2012, PTDC/BBB-IMG/2137/2012, Pest OE/EEI/LA0021/2013, Pest-
OE/EEI/LA0009/2013, and NIHNIBIBP41EB015896.References
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