Assessing interactions in the brain with exact low-resolution electromagnetic tomography

  • Roberto D. Pascual-Marqui
    The KEY Institute for Brain-Mind Research, University Hospital of Psychiatry, Lenggstrasse 31, 8032 Zurich, Switzerland
  • Dietrich Lehmann
    The KEY Institute for Brain-Mind Research, University Hospital of Psychiatry, Lenggstrasse 31, 8032 Zurich, Switzerland
  • Martha Koukkou
    The KEY Institute for Brain-Mind Research, University Hospital of Psychiatry, Lenggstrasse 31, 8032 Zurich, Switzerland
  • Kieko Kochi
    The KEY Institute for Brain-Mind Research, University Hospital of Psychiatry, Lenggstrasse 31, 8032 Zurich, Switzerland
  • Peter Anderer
    Department of Psychiatry and Psychotherapy, Medical University of Vienna, Austria
  • Bernd Saletu
    Department of Psychiatry and Psychotherapy, Medical University of Vienna, Austria
  • Hideaki Tanaka
    Department of Neurology, Dokkyo University School of Medicine, Tochigi, Japan
  • Koichi Hirata
    Department of Neurology, Dokkyo University School of Medicine, Tochigi, Japan
  • E. Roy John
    Brain Research Laboratories, Department of Psychiatry, New York University School of Medicine, NY, USA
  • Leslie Prichep
    Brain Research Laboratories, Department of Psychiatry, New York University School of Medicine, NY, USA
  • Rolando Biscay-Lirio
    Institute for Cybernetics, Mathematics, and Physics, Havana, Cuba
  • Toshihiko Kinoshita
    Department of Neuropsychiatry, Kansai Medical University Hospital, 10-15, Fumizono-cho, Moriguchi, Osaka, 570-8507, Japan

説明

<jats:p>Scalp electric potentials (electroencephalogram; EEG) are contingent to the impressed current density unleashed by cortical pyramidal neurons undergoing post-synaptic processes. EEG neuroimaging consists of estimating the cortical current density from scalp recordings. We report a solution to this inverse problem that attains exact localization: exact low-resolution brain electromagnetic tomography (eLORETA). This non-invasive method yields high time-resolution intracranial signals that can be used for assessing functional dynamic connectivity in the brain, quantified by coherence and phase synchronization. However, these measures are non-physiologically high because of volume conduction and low spatial resolution. We present a new method to solve this problem by decomposing them into instantaneous and lagged components, with the lagged part having almost pure physiological origin.</jats:p>

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