» Articles » PMID: 23840188

Cross-frequency Coupling in Real and Virtual Brain Networks

Overview
Specialty Biology
Date 2013 Jul 11
PMID 23840188
Citations 79
Authors
Affiliations
Soon will be listed here.
Abstract

Information processing in the brain is thought to rely on the convergence and divergence of oscillatory behaviors of widely distributed brain areas. This information flow is captured in its simplest form via the concepts of synchronization and desynchronization and related metrics. More complex forms of information flow are transient synchronizations and multi-frequency behaviors with metrics related to cross-frequency coupling (CFC). It is supposed that CFC plays a crucial role in the organization of large-scale networks and functional integration across large distances. In this study, we describe different CFC measures and test their applicability in simulated and real electroencephalographic (EEG) data obtained during resting state. For these purposes, we derive generic oscillator equations from full brain network models. We systematically model and simulate the various scenarios of CFC under the influence of noise to obtain biologically realistic oscillator dynamics. We find that (i) specific CFC-measures detect correctly in most cases the nature of CFC under noise conditions, (ii) bispectrum (BIS) and bicoherence (BIC) correctly detect the CFCs in simulated data, (iii) empirical resting state EEG show a prominent delta-alpha CFC as identified by specific CFC measures and the more classic BIS and BIC. This coupling was mostly asymmetric (directed) and generally higher in the eyes closed (EC) than in the eyes open (EO) condition. In conjunction, these two sets of measures provide a powerful toolbox to reveal the nature of couplings from experimental data and as such allow inference on the brain state dependent information processing. Methodological advantages of using CFC measures and theoretical significance of delta and alpha interactions during resting and other brain states are discussed.

Citing Articles

Deciphering temporal scales of visual awareness: insights from flicker frequency modulation in continuous flash suppression.

Singhal I, Srinivasan N Neurosci Conscious. 2025; 2025(1):niaf005.

PMID: 40051812 PMC: 11884739. DOI: 10.1093/nc/niaf005.


What can neurofeedback and transcranial alternating current stimulation reveal about cross-frequency coupling?.

Orendacova M, Kvasnak E Front Neurosci. 2025; 19:1465773.

PMID: 40012676 PMC: 11861218. DOI: 10.3389/fnins.2025.1465773.


The classification of absence seizures using power-to-power cross-frequency coupling analysis with a deep learning network.

Medvedev A, Lehmann B Front Neuroinform. 2025; 19:1513661.

PMID: 39995596 PMC: 11847813. DOI: 10.3389/fninf.2025.1513661.


Artificial Intelligence and Neuroscience: Transformative Synergies in Brain Research and Clinical Applications.

Onciul R, Tataru C, Dumitru A, Crivoi C, Serban M, Covache-Busuioc R J Clin Med. 2025; 14(2).

PMID: 39860555 PMC: 11766073. DOI: 10.3390/jcm14020550.


Exploring neural oscillations during speech perception via surrogate gradient spiking neural networks.

Bittar A, Garner P Front Neurosci. 2024; 18:1449181.

PMID: 39385848 PMC: 11461475. DOI: 10.3389/fnins.2024.1449181.


References
1.
Schack B, Klimesch W . Frequency characteristics of evoked and oscillatory electroencephalic activity in a human memory scanning task. Neurosci Lett. 2002; 331(2):107-10. DOI: 10.1016/s0304-3940(02)00846-7. View

2.
Tsuno N, Shigeta M, Hyoki K, Kinoshita T, Ushijima S, Faber P . Spatial organization of EEG activity from alertness to sleep stage 2 in old and younger subjects. J Sleep Res. 2002; 11(1):43-51. DOI: 10.1046/j.1365-2869.2002.00288.x. View

3.
Deco G, Jirsa V, McIntosh A, Sporns O, Kotter R . Key role of coupling, delay, and noise in resting brain fluctuations. Proc Natl Acad Sci U S A. 2009; 106(25):10302-7. PMC: 2690605. DOI: 10.1073/pnas.0901831106. View

4.
Elbert T, Ray W, Kowalik Z, SKINNER J, Graf K, Birbaumer N . Chaos and physiology: deterministic chaos in excitable cell assemblies. Physiol Rev. 1994; 74(1):1-47. DOI: 10.1152/physrev.1994.74.1.1. View

5.
Wacker M, Putsche P, Witte H . Time-variant analysis of linear and non-linear phase couplings of and between frequency components of EEG burst patterns in full-term newborns. Annu Int Conf IEEE Eng Med Biol Soc. 2010; 2010:1706-9. DOI: 10.1109/IEMBS.2010.5626845. View