Dietmar Cordes1,2, Muhammad Kaleem3, Xiaowei Zhuang1, Karthik Sreenivasan1, Zhengshi Yang1, Tim Curran2, and Virendra Mishra1
1Cleveland Clinic Lou Ruvo Center for Brain Health, Las Vegas, NV, United States, 2University of Colorado, Boulder, CO, United States, 3University of Management & Technology, Lahore, Pakistan
Synopsis
Energy-period relationships and frequency content of
Intrinsic Mode Functions (IMFs) were studied in deconvolved fMRI data using a
blind deconvolution method. Results are shown for multiband MB8 resting-state
data collected with a TR of 0.765s for a group of 22 healthy subjects. Findings
of the present study suggest that high-frequency content in the major primary
resting-state networks (such as the Default Mode Network, Visual Network,
Auditory Network, or Fronto-Parietal network) is rather limited and not
supported to be of any significance for high frequencies larger than 0.21 Hz,
whether in BOLD data or blind-deconvolved data.
Introduction
Resting-state functional
networks were traditionally computed by low-pass-filtering data retaining
frequencies less than 0.1Hz1. Recently, it was argued that high
frequencies larger than 0.1Hz may also contribute to functional connectivity
for major resting-state networks2,3. To shed more light on this question,
we applied a blind-deconvolution method to resting-state data that were
collected with a high sampling rate, allowing to investigate the frequency
content up to 0.65Hz. Rather than relying on user-defined frequency bands, we
use Empirical Mode Decomposition (EMD)4,5 to study the natural
occurring frequency bands of major resting-state networks after blind deconvolution
and compare results with the original BOLD data.Methods
FMRI was performed on
22 healthy subjects in a 3T Siemens MRI scanner (32-channel head coil, MB8 EPI,
TR 765ms, TE 30ms, flip 44deg, 2380 time frames). The data have been minimally preprocessed to
avoid contamination of high-frequency artifacts that could have been
potentially introduced by improper preprocessing. Identification of
resting-state networks was done by using group ICA. For blind deconvolution we used the method by
Wu et al.6 Briefly, each fMRI time series was treated as a
convolution of point processes with unknown hemodynamic response function (HRF)
and delay time. The HRF was approximated by a linear combination of the
canonical HRF, its first order and second order derivative. The expansion
coefficients were obtained by least square minimization, and the best time
delay (for each voxel) was obtained by covariance minimization of the residual.
Deconvolution was then carried out using the Wiener filter in the Fourier
domain. After deconvolution group ICA (using the FastICA algorithm7)
was used to obtain 30 spatial components. Using visual inspection, the Default
Mode Network (DMN), the primary and secondary visual networks (VIS, VIS2), the
auditory network (AUD) and the left/right frontoparietal network (lFPN, rFPN)
were identified. The corresponding time courses were computed by spatial
regression and then further decomposed into Intrinsic Mode Functions (IMFs)
using EMD.Results
Fig.1 shows time
series characteristics of the first 9 IMFs for the DMN after deconvolution (Fig.1A-C).
Comparison to the original BOLD data are shown in Fig.1D-F. Note that IMF1 and
IMF2 have large amplitudes of oscillation (Fig.1A) compared to the original
data (Fig.1D). Furthermore, the frequency range of IMF1 is limited to the
intermediate frequencies (Fig.1B), which is quite different than the wide frequency spectrum
of IMF1 of the BOLD data (Fig.1E). Fig.1C and Fig.1F show the energy-period relationship of the IMFs superimposed on a white noise
spectrum (black dots). Note that the mean energies of IMF1 and IMF2, which
represent mostly frrquency components above 0.1Hz, are significantly increased
for the deconvolved data. However, the corresponding mean energy-period points
do not extend above the white noise spectrum. Fig.2 shows the energy-period
signatures averaged over all 6 resting-state networks showing that the
deconvolved data (Fig.2A) have an IMF signature that is closer to the white
noise distribution when compared to the signature of the BOLD data (Fig2.B). To
obtain more frequency-specific information, we also high-pass filtered
the IMFs and computed the related spatial maps by regression on the original deconvolved
data. Table 1 lists the highest frequency content of each network to achieve a
Dice similarity coefficient larger than 0.7.Discussion
IMFs of deconvolved data are characterized by
a lower mean frequency and lower frequency range than corresponding IMFs of
BOLD data. From the energy-period plots and Fig.1B vs Fig.1E, it is apparent that the period is
increased for all IMFs of the deconvolved data. Attenuation of high frequencies
larger than 0.3 Hz can be explained by the Wiener filter to prevent noise
amplification. In contrast, the energy of IMF1 and, to a lesser degree, IMF2
are increased compared to the BOLD data. For all other IMFs the energy is
relatively similar to the BOLD data. It appears that a large portion of the
amplified frequencies by deconvolution is not network associated and only increases
the energy density of IMF1 and IMF2, and network-associated frequencies are not
shifted to higher frequencies. From the energy-period relationship, it can also
be seen that blind deconvolution leads to signatures that are closer to signatures
of white noise data.Conclusion
This study suggests
that blind deconvolution amplifies mostly intermediate frequencies (0.2 Hz-0.3
Hz) which are not network-related. Also, high frequencies larger than 0.3 Hz
are attenuated by the Wiener filter, and energy-period signatures of IMFs are
shifted more towards the diagonal line that is associated with white noise
processes. Low frequencies less than 0.1 Hz provide the largest contribution to
the studied networks, and none of the primary networks could be associated with any significant frequency content above 0.21 Hz.Acknowledgements
This research project was supported by the NIH
(COBRE grant 1P20GM109025 and 1R01EB014284).References
[1] Cordes D, et
al. Frequencies contributing to functional connectivity in the cerebral cortex
in resting-state data. AJNR 2001, 22:1326-1333.
[2] Niazy RK, et
al. Spectral characteristics of resting-state networks. Prog. Brain Res. 2011,
193:259-276.
[3] Chen JE, Glover
GH. BOLD fractional contribution to resting-state functional connectivity above
0.1Hz. NeuroImage 2014, 107:207-218.
[4] Flandrin P, et
al. Empirical mode decomposition as a filter bank, IEEE Sig. Proc. Letters
2004, 11(2), 112-114.
[5] Huang NE, et
al. The empirical mode decomposition and the Hilbert spectrum for nonlinear and
non-stationary time series analysis. Proc. R. Soc. Lond. 1998, A 454, 903-995.
[6] Wu GR, et al. A blind
deconvolution approach to recover effective connectivity brain networks from
resting state fMRI data. Medical Image Analysis 2013, 17:365-374.
[7] Hyvärinen A. Fast and
Robust Fixed-Point Algorithms for Independent Component Analysis. IEEE Transactions on Neural Networks 1999, 10(3):626-634.