Elsevier

NeuroImage

Volume 22, Issue 4, August 2004, Pages 1432-1437
NeuroImage

Detection of very high correlation in the alpha band between temporal regions of the human brain using MEG

https://doi.org/10.1016/j.neuroimage.2004.04.016Get rights and content

Abstract

It is generally believed that alpha band (8–12 Hz) electric and magnetic activity in the area of the left and right temporal regions in the human brain are at best poorly correlated. There are no previous reports of very high alpha band correlation between left and right temporal regions by magnetoencephalography (MEG) or electroencephalography (EEG). We present whole head magnetoencephalography (MEG) results that demonstrate that, for temporal channels in the majority of healthy subjects tested, the alpha band signals are highly to very highly correlated and are antiparallel in direction. A correlation as high as −0.97 was found for a limited time in one subject. We suggest that the correlation found may be the consequence of strong direct or indirect coupling between homologue areas in left and right temporal regions rather than a common source. The correlation may provide a valuable index of loss of connectivity in the brain due to disease as well providing valuable insight to brain function and deserves further investigation.

Introduction

Highly correlated anterior–posterior electroencephalography (EEG) signals in the alpha band (8–12 Hz) have been reported for some time (e.g. Leocani et al., 2000, Manshanden et al., 2002, Nunez et al., 1997). In some cases, correlations as high as 0.9 have been measured. But there have been no reports of high or very high correlation between left and right temporal signals in the alpha band. Indeed, although there are many publications on synchronization measures between various regions of the brain, there are few publications by any sort of synchronization measures—be it coherence, phase synchronization, correlation or any one of a host of other synchronization measures—between the temporal regions.

A few publications do discuss results from inter-temporal region synchronization measures using EEG. Duffy et al (1996) studied the age effects of interhemispheric EEG coherence including between temporal regions in the alpha band for both eyes-open and eyes-closed brain states. They found the alpha band inter-temporal region coherence to be weak. Winterer et al (2001) studied EEG coherence with eyes closed as part of a genetic risk for schizophrenia study. They reported very high coherence in the delta band between posterior temporal lobe regions but did not report similarly high coherence for the alpha band. Moorehouse et al. (2002) found low inter-temporal coherence during sleep in adolescent girls at high risk for depression in the EEG theta and delta bands. Knyazeva et al (1999) found that a single grating that extended across the vertical meridian significantly increased the EEG interhemispheric coherence in normal adult subjects in the gamma band.

As is well known, there are several sources of alpha band signals in the human brain. The most familiar is probably the alpha rhythm, which emanates from the visual cortex. However, the mu and tau rhythms are also in the alpha band. Detection of reactive magnetic rhythm near 10 Hz in the human auditory cortex has also been reported but signal correlation between different magnetoencephalography (MEG) channels was not considered and the frequency range (6.5–9.5 Hz) is different than the one used herein (Lehtela et al., 1997).

Using MEG, we have detected epochs of high to very high correlation between at least a few left and right temporal MEG channels in most of 10 healthy controls during an eyes-closed no-task condition. In two of the subjects (204 and 210), the correlation was very high for extended periods and extended superior to the temporal regions. With further study, the detected correlation between temporal regions may be useful in understanding the communication between temporal regions in healthy individuals. Also, loss of correlation can be indicative of loss of connectivity in the brain. Loss of connectivity can be an indication of disease and other sources of neurological deficits. Thus, the detected high correlation may be of help in studying and monitoring when loss of connectivity is a problem including diseases such as multiple sclerosis.

Section snippets

Methods

Ten healthy volunteers (age 23–48 years, four females) were scanned for 5 min with eyes closed and then for 3 min with eyes open. They were seated in a 151-channel MEG scanner (CTF Systems, Vancouver, Canada; Vrba, 1996). The no-task eyes-closed data were acquired after 15 min of visually evoked field data using the standard reversing checkerboard pattern (Niedermeyer and Lopes da Silva, 1993). Electrooculography (EOG) data were acquired simultaneously on all subjects.

The subjects were scanned

Results

Fig. 1 shows the correlation maps for each of the subjects for the 4-s epochs extracted from near the start of each subject's scan. An expected feature common to all the subjects is a high positive correlation along the midline of each map. This high positive correlation is at least in part due to physical adjacent coils picking up the same signal (similar to the volume conduction effect).

Moving away from the midline, the correlations change from positive values to negative ones. The map for

Discussion

When left and right temporal channels of the MEG scanner produce signals which are nearly mirror images of each other, such as in Fig. 2, it is natural to ask if the correlation could be due to some sort of artifact.

However, many characteristics of the data demonstrate the correlation is physiological in nature:

  • (1)

    the alpha band power and correlation drops substantially when the eyes are opened as shown in Fig. 2, Fig. 3, Fig. 4;

  • (2)

    weekly calibrations of our MEG scanner show negligible cross talk

Conclusions

Most of the 10 healthy volunteers undergoing a MEG scan with eyes closed clearly demonstrated high correlation between left and right temporal channels. It is suggested the temporal correlation may be due to anterior-pointing current dipoles in each superior temporal gyrus and adjacent regions that are tightly correlated by direct or indirect cortical–cortical interconnections. Monitoring the loss of correlation between the temporal lobes may provides a valuable way of monitoring disease and

Acknowledgements

We thank H. Vrenken, J.J.G. Geurts, B. van Oosten, B. Jelles and C.H. Polman for their input. We would also like to thank Peter Jan Ris, Ilonka Zuiderwijk, Geert deVos and Jeroen Verbunt. K.S.C. was funded by Drs. D.W. Paty and D.K.B. Li of the MS/MRI group at the University of British Columbia and VSM (CTF) Systems Inc.

References (15)

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