The Influence of EEG References on the Analysis of Spatio-Temporal Interrelation Patterns (original) (raw)

Brain connectivity at different time-scales measured with EEG

Philosophical Transactions of The Royal Society B: Biological Sciences, 2005

We present an overview of different methods for decomposing a multichannel spontaneous electroencephalogram (EEG) into sets of temporal patterns and topographic distributions. All of the methods presented here consider the scalp electric field as the basic analysis entity in space. In time, the resolution of the methods is between milliseconds (time-domain analysis), subseconds (time-and frequency-domain analysis) and seconds (frequency-domain analysis). For any of these methods, we show that large parts of the data can be explained by a small number of topographic distributions. Physically, this implies that the brain regions that generated one of those topographies must have been active with a common phase. If several brain regions are producing EEG signals at the same time and frequency, they have a strong tendency to do this in a synchronized mode. This view is illustrated by several examples (including combined EEG and functional magnetic resonance imaging (fMRI)) and a selective review of the literature. The findings are discussed in terms of short-lasting binding between different brain regions through synchronized oscillations, which could constitute a mechanism to form transient, functional neurocognitive networks.

Mapping EEG-potentials on the surface of the brain: A strategy for uncovering cortical sources

Brain Topography, 1997

This paper describes a uniform method for calculating the interpolation of scalp EEG potential distribution, the current source density (CSD), the cortical potential distribution (cortical mapping) and the CSD of the cortical potential distribution. It will be shown that interpolation and deblurring methods such as CSD or cortical mapping are not independent of the inverse problem in potential theory. Not only the resolution but also the accuracy of these techniques, especially those of deblurring, depend greatly on the spatial sampling rate (i.e., the number of electrodes). Using examples from simulated and real (64 channels) data it can be shown that the application of more than 100 EEG channels is not only favourable but necessary to guarantee a reasonable accuracy in the calculations of CSD or cortical mapping. Likewise, it can be shown that using more than 250 electrodes does not improve the resolution.

The spatial resolution of scalp EEG

Neurocomputing, 2001

The scalp electroencephalogram (EEG) exhibits spatiotemporal dynamics re#ecting synchronous dendritic activity of cortical pyramidal neurons. Recent advances in EEG acquisition and electric head modeling are improving the spatial resolution of scalp EEG, but the skull remains an obstacle. We use lead "eld theory to quantify the spatial resolution of scalp EEG, contrasting two electrode spacings and two values of skull conductivity. We show that, without cortical constraints, 19-electrode EEG systems have optimal spatial resolution near 22}37 cm, while 129-electrode systems have 6}8 cm. These results emphasize the bene"ts of more electrodes, but also the need for methods of measuring local skull conductivity.

Cross-correlation of instantaneous amplitudes of field potential oscillations: A straightforward method to estimate the directionality and lag between brain areas

Journal of Neuroscience Methods, 2010

Researchers performing multi-site recordings are often interested in identifying the directionality of functional connectivity and estimating lags between sites. Current techniques for determining directionality require spike trains or involve multivariate autoregressive modeling. However, it is often difficult to sample large numbers of spikes from multiple areas simultaneously, and modeling can be sensitive to noise. A simple, model-independent method to estimate directionality and lag using local field potentials (LFPs) would be of general interest. Here we describe such a method using the cross-correlation of the instantaneous amplitudes of filtered LFPs. The method involves four steps. First, LFPs are band-pass filtered; second, the instantaneous amplitude of the filtered signals is calculated; third, these amplitudes are cross-correlated and the lag at which the cross-correlation peak occurs is determined; fourth, the distribution of lags obtained is tested to determine if it differs from zero. This method was applied to LFPs recorded from the ventral hippocampus and the medial prefrontal cortex in awake behaving mice. The results demonstrate that the hippocampus leads the mPFC, in good agreement with the time lag calculated from the phase locking of mPFC spikes to vHPC LFP oscillations in the same dataset. We also compare the amplitude cross-correlation method to partial directed coherence, a commonly used multivariate autoregressive model-dependent method, and find that the former is more robust to the effects of noise. These data suggest that the cross-correlation of instantaneous amplitude of filtered LFPs is a valid method to study the direction of flow of information across brain areas.

Spatiotemporal scales and links between electrical neuroimaging modalities

Medical & Biological Engineering & Computing, 2011

Recordings of brain electrophysiological activity provide the most direct reflect of neural function. Information contained in these signals varies as a function of the spatial scale at which recordings are done: from single cell recording to large scale macroscopic fields, e.g., scalp EEG. Microscopic and macroscopic measurements and models in Neuroscience are often in conflict. Solving this conflict might require the developments of a sort of bio-statistical physics, a framework for relating the microscopic properties of individual cells to the macroscopic or bulk properties of neural circuits. Such a framework can only emerge in Neuroscience from the systematic analysis and modeling of the diverse recording scales from simultaneous measurements. In this article we briefly review the different measurement scales and models in modern neuroscience to try to identify the sources of conflict that might ultimately help to create a unified theory of brain electromagnetic fields. We argue that seen the different recording scales, from the single cell to the large scale fields measured by the scalp electroencephalogram, as derived from a unique physical magnitude-the electric potential that is measured in all cases-might help to conciliate microscopic and macroscopic models of neural function as well as the animal and human neuroscience literature.