TY - JOUR
T1 - Novel multivariate methods to track frequency shifts of neural oscillations in EEG/MEG recordings
AU - Vidaurre, C.
AU - Gurunandan, K.
AU - Idaji, M. Jamshidi
AU - Nolte, G.
AU - Gómez, M.
AU - Villringer, A.
AU - Müller, K. R.
AU - Nikulin, V. V.
N1 - Publisher Copyright:
© 2023
PY - 2023/8/1
Y1 - 2023/8/1
N2 - Instantaneous and peak frequency changes in neural oscillations have been linked to many perceptual, motor, and cognitive processes. Yet, the majority of such studies have been performed in sensor space and only occasionally in source space. Furthermore, both terms have been used interchangeably in the literature, although they do not reflect the same aspect of neural oscillations. In this paper, we discuss the relation between instantaneous frequency, peak frequency, and local frequency, the latter also known as spectral centroid. Furthermore, we propose and validate three different methods to extract source signals from multichannel data whose (instantaneous, local, or peak) frequency estimate is maximally correlated to an experimental variable of interest. Results show that the local frequency might be a better estimate of frequency variability than instantaneous frequency under conditions with low signal-to-noise ratio. Additionally, the source separation methods based on local and peak frequency estimates, called LFD and PFD respectively, provide more stable estimates than the decomposition based on instantaneous frequency. In particular, LFD and PFD are able to recover the sources of interest in simulations performed with a realistic head model, providing higher correlations with an experimental variable than multiple linear regression. Finally, we also tested all decomposition methods on real EEG data from a steady-state visual evoked potential paradigm and show that the recovered sources are located in areas similar to those previously reported in other studies, thus providing further validation of the proposed methods.
AB - Instantaneous and peak frequency changes in neural oscillations have been linked to many perceptual, motor, and cognitive processes. Yet, the majority of such studies have been performed in sensor space and only occasionally in source space. Furthermore, both terms have been used interchangeably in the literature, although they do not reflect the same aspect of neural oscillations. In this paper, we discuss the relation between instantaneous frequency, peak frequency, and local frequency, the latter also known as spectral centroid. Furthermore, we propose and validate three different methods to extract source signals from multichannel data whose (instantaneous, local, or peak) frequency estimate is maximally correlated to an experimental variable of interest. Results show that the local frequency might be a better estimate of frequency variability than instantaneous frequency under conditions with low signal-to-noise ratio. Additionally, the source separation methods based on local and peak frequency estimates, called LFD and PFD respectively, provide more stable estimates than the decomposition based on instantaneous frequency. In particular, LFD and PFD are able to recover the sources of interest in simulations performed with a realistic head model, providing higher correlations with an experimental variable than multiple linear regression. Finally, we also tested all decomposition methods on real EEG data from a steady-state visual evoked potential paradigm and show that the recovered sources are located in areas similar to those previously reported in other studies, thus providing further validation of the proposed methods.
KW - correlation optimization
KW - decomposition methods
KW - electroencephalography (EEG)
KW - instantaneous frequency
KW - local frequency
KW - magnetoencephalography (MEG)
KW - multimodal methods
KW - multiple linear regression
KW - multivariate methods
KW - Peak frequency
KW - source separation
KW - spatial filters
KW - spectral centroid
UR - http://www.scopus.com/inward/record.url?scp=85162831712&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2023.120178
DO - 10.1016/j.neuroimage.2023.120178
M3 - Article
C2 - 37236554
AN - SCOPUS:85162831712
SN - 1053-8119
VL - 276
JO - NeuroImage
JF - NeuroImage
M1 - 120178
ER -