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J Neurophysiol 93: 2864-2872, 2005. First published December 15, 2004; doi:10.1152/jn.00721.2004
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Cortical and Subcortical Correlates of Electroencephalographic Alpha Rhythm Modulation

Bernd Feige1, Klaus Scheffler2, Fabrizio Esposito3, Francesco Di Salle4, Jürgen Hennig5 and Erich Seifritz6,7

1Department of Psychiatry and Psychotherapy, University of Freiburg, Freiburg, Germany; 2MR-Physics, Department of Medical Radiology, University of Basel, Basel, Switzerland; 3Second Division of Neurology, Second University of Naples, Naples, Italy; 4Department of Neurological Sciences, Division of Neuroradiology, University of Naples Federico II, Naples, Italy; 5Department of Radiological Research and Medical Physics, University of Freiburg, Freiburg, Germany; 6Department of Psychiatry, University of Basel, Basel, Switzerland; and 7University Hospital of Clinical Psychiatry, University of Bern, Bern, Switzerland

Submitted 14 July 2004; accepted in final form 8 December 2004

Neural correlates of electroencephalographic (EEG) alpha rhythm are poorly understood. Here, we related EEG alpha rhythm in awake humans to blood-oxygen-level-dependent (BOLD) signal change determined by functional magnetic resonance imaging (fMRI). Topographical EEG was recorded simultaneously with fMRI during an open versus closed eyes and an auditory stimulation versus silence condition. EEG was separated into spatial components of maximal temporal independence using independent component analysis. Alpha component amplitudes and stimulus conditions served as general linear model regressors of the fMRI signal time course. In both paradigms, EEG alpha component amplitudes were associated with BOLD signal decreases in occipital areas, but not in thalamus, when a standard BOLD response curve (maximum effect at ~6 s) was assumed. The part of the alpha regressor independent of the protocol condition, however, revealed significant positive thalamic and mesencephalic correlations with a mean time delay of ~2.5 s between EEG and BOLD signals. The inverse relationship between EEG alpha amplitude and BOLD signals in primary and secondary visual areas suggests that widespread thalamocortical synchronization is associated with decreased brain metabolism. While the temporal relationship of this association is consistent with metabolic changes occurring simultaneously with changes in the alpha rhythm, sites in the medial thalamus and in the anterior midbrain were found to correlate with short time lag. Assuming a canonical hemodynamic response function, this finding is indicative of activity preceding the actual EEG change by some seconds.


Address for reprint requests and other correspondence: B. Feige, Dept. of Psychiatry and Psychotherapy, Hauptstraße 5, 79104 Freiburg, Germany (E-mail: Bernd.Feige{at}gmx.net)




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