From Scalp to Source: Precise Phase Retrieval of Intracerebral Epileptic Sources Based on Surface EEG
W skrócie
[Preprint - wstępne wyniki] Naukowcy opracowali nową metodę (Gabor-Nelson) do odtwarzania aktywności głębokich struktur mózgu z nieinwazyjnego badania EEG (elektrod na skórze głowy), bez konieczności zaawansowanego skanowania MRI. Metoda ta osiągnęła dokładność porównywalną z tradycyjnymi metodami, uzyskując błąd pomiaru fazy poniżej 9 stopni w badaniach na zwłokach i korelację około 0,80 u pacjentów. Nowe podejście mogłoby umożliwić rozszerzenie dostępu do zaawansowanych terapii neurostymulacyjnych dla pacjentów z epilepsją na całym świecie.
Oryginalny abstract (angielski)
Accurate phase tracking of deep-brain activity is critical for effective closed-loop and phase-locked neuromodulation therapies. However, direct access to deep neural phase through intracranial recordings remains clinically restrictive due to the invasiveness. Here we validate and clinically benchmark the Gabor-Nelson (GN) dipole estimation method for reconstructing deep-brain oscillatory phase from non-invasive scalp EEG. GN is a geometry-based, imaging-independent approach that offers computationally efficient dipole reconstruction and has rarely been applied to source-level phase estimation in human neuroscience. We compared GN with an established MRI-informed Inverse Solution (IS) method using a three-stage reconstruction pipeline consisting of dipole modeling, dimensionality reduction, and frequency-dependent phase-delay correction. Validation is performed using (i) cadaveric recordings, where known ground-truth seizure waveforms were replayed through implanted deep electrodes, and (ii) simultaneous scalp EEG and SEEG recordings in human patients, where pseudo-ground truth was approximated via the intracranial contacts. GN achieved phase accuracy and signal fidelity comparable to IS across both datasets despite requiring no anatomical imaging. In cadaver recordings, phase-corrected reconstruction correlations exceeded r > 0.91 and ΔΦ < 9° in mean phase error. In patient SEEG data, GN reached up to r ≈ 0.80 with phase offsets suitable for neuromodulatory timing. GN offers a viable, low-barrier, imaging-independent alternative to traditional inverse modeling for non-invasive seizure phase tracking. This framework opens pathways for scalable, phase-locked and closed-loop stimulation therapies in epilepsy and potentially other network-based brain disorders.
Metadane publikacji
Journal
Preprint (medRxiv/bioRxiv)
Data publikacji
20.08.2026
DOI
10.64898/2026.08.16.745081
Europe PMC ID
PPR1302330
Autorzy
Furuglyas K, Huszar-Kis M, Horvath B, Pejin A, Forgo N, Lango I, Singla S, Gorog M, Vass P, Chadaide Z