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Imaging of brain electric field networks with spatially resolved EEG.

Lawrence R Frank | Vitaly L Galinsky | Olave Krigolson | Susan Tapert | Stephan Bickel | Antigona Martinez
eLife | 2025

We present a method for spatially resolving the electric field potential throughout the entire volume of the human brain from electroencephalography (EEG) data. The method is not a variation of the well-known 'source reconstruction' methods, but rather a direct solution to the EEG inverse problem based on our recently developed model for brain waves that demonstrates the inadequacy of the standard 'quasi-static approximation' that has fostered the belief that such a reconstruction is not physically possible. The method retains the high temporal/frequency resolution of EEG, yet has spatial resolution comparable to (or better than) functional MRI (fMRI), without its significant inherent limitations. The method is validated using simultaneous EEG/fMRI data in healthy subjects, intracranial EEG data in epilepsy patients, comparison with numerical simulations, and a direct comparison with standard state-of-the-art EEG analysis in a well-established attention paradigm. The method is then demonstrated on a very large cohort of subjects performing a standard gambling task designed to activate the brain's 'reward circuit'. The technique uses the output from standard extant EEG systems and thus has potential for immediate benefit to a broad range of important basic scientific and clinical questions concerning brain electrical activity. By offering an inexpensive and portable alternative to fMRI, it provides a realistic methodology to efficiently promote the democratization of medicine.

Pubmed ID: 40472276

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Antibodies used in this publication

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Associated grants

  • Agency: NIH HHS, United States
    Id: U24 AA021695
  • Agency: NIDCD NIH HHS, United States
    Id: R01DC019979
  • Agency: NIA NIH HHS, United States
    Id: R01 AG054049
  • Agency: Natural Sciences and Engineering Research Council of Canada,
    Id: Discovery Grant RGPIN 2016-0943
  • Agency: NIH HHS, United States
    Id: U01 DA041089
  • Agency: NIMH NIH HHS, United States
    Id: R21 MH123875
  • Agency: National Science Foundation,
    Id: AGS-2114860
  • Agency: NIDA NIH HHS, United States
    Id: R01 DA057567
  • Agency: NIH HHS, United States
    Id: U01 AA021692
  • Agency: NIH HHS, United States
    Id: R01-AG079280
  • Agency: NIDCD NIH HHS, United States
    Id: R01 DC019979
  • Agency: NIH HHS, United States
    Id: R01- AG054049
  • Agency: NIAAA NIH HHS, United States
    Id: U01 AA021692
  • Agency: NIA NIH HHS, United States
    Id: R01 AG079280
  • Agency: Simons Foundation Autism Research Initiative,
    Id: AR-HUMAN- 00004264
  • Agency: NIDA NIH HHS, United States
    Id: U01 DA041089
  • Agency: National Science Foundation,
    Id: ACI-1550405
  • Agency: NIH HHS, United States
    Id: R21MH123875
  • Agency: NIAAA NIH HHS, United States
    Id: U24 AA021695
  • Agency: NIH HHS, United States
    Id: R01 DA057567

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This is a list of tools and resources that we have found mentioned in this publication.


Analysis of Functional NeuroImages (tool)

RRID:SCR_005927

Set of (mostly) C programs that run on X11+Unix-based platforms (Linux, Mac OS X, Solaris, etc.) for processing, analyzing, and displaying functional MRI (FMRI) data defined over 3D volumes and over 2D cortical surface meshes. AFNI is freely distributed as source code plus some precompiled binaries.

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Low Resolution Electromagnetic Tomography (software resource)

RRID:SCR_007077

Software package for functional imaging of human brain. Used to compute three dimensional distribution of electric neuronal activity from non-invasive measurements of scalp electric potential differences with high time resolution in millisecond range. Non-invasive intracranial time series are used for studying functional dynamic connectivity.. Current software version includes two new, improved variants of the original method: standardized (sLORETA) and exact (eLORETA). The new methods are characterized by exact localization when tested with point sources. Due to the fact that these methods are multivariate tomographies that are solutions to the inverse EEG problem, and that they are linear in nature, they will produce a low spatial resolution image for any distribution of activity. This property is not shared by naive one-at-a-time single dipole techniques.

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