Improved Dipole Source Localization from Simultaneous MEG-EEG Data by Combining a Global Optimization Algorithm with a Local Parameter Search: A Brain Phantom Study.

EEG MEG dipole localization global optimization simulated annealing

Journal

Bioengineering (Basel, Switzerland)
ISSN: 2306-5354
Titre abrégé: Bioengineering (Basel)
Pays: Switzerland
ID NLM: 101676056

Informations de publication

Date de publication:
06 Sep 2024
Historique:
received: 18 08 2024
revised: 03 09 2024
accepted: 04 09 2024
medline: 27 9 2024
pubmed: 27 9 2024
entrez: 27 9 2024
Statut: epublish

Résumé

Dipole localization, a fundamental challenge in electromagnetic source imaging, inherently constitutes an optimization problem aimed at solving the inverse problem of electric current source estimation within the human brain. The accuracy of dipole localization algorithms is contingent upon the complexity of the forward model, often referred to as the head model, and the signal-to-noise ratio (SNR) of measurements. In scenarios characterized by low SNR, often corresponding to deep-seated sources, existing optimization techniques struggle to converge to global minima, thereby leading to the localization of dipoles at erroneous positions, far from their true locations. This study presents a novel hybrid algorithm that combines simulated annealing with the traditional quasi-Newton optimization method, tailored to address the inherent limitations of dipole localization under low-SNR conditions. Using a realistic head model for both electroencephalography (EEG) and magnetoencephalography (MEG), it is demonstrated that this novel hybrid algorithm enables significant improvements of up to 45% in dipole localization accuracy compared to the often-used dipole scanning and gradient descent techniques. Localization improvements are not only found for single dipoles but also in two-dipole-source scenarios, where sources are proximal to each other. The novel methodology presented in this work could be useful in various applications of clinical neuroimaging, particularly in cases where recordings are noisy or sources are located deep within the brain.

Identifiants

pubmed: 39329639
pii: bioengineering11090897
doi: 10.3390/bioengineering11090897
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : National Institute of Neurological Disorders & Stroke
ID : R01NS104116-01A1

Auteurs

Subrat Bastola (S)

Bioengineering Department, The University of Texas at Arlington, Arlington, TX 76019, USA.

Saeed Jahromi (S)

Bioengineering Department, The University of Texas at Arlington, Arlington, TX 76019, USA.
Neuroscience Research Center, Jane and John Justin Institute for Mind Health, Cook Children's Health Care System, Fort Worth, TX 76104, USA.

Rupesh Chikara (R)

Bioengineering Department, The University of Texas at Arlington, Arlington, TX 76019, USA.
Neuroscience Research Center, Jane and John Justin Institute for Mind Health, Cook Children's Health Care System, Fort Worth, TX 76104, USA.

Steven M Stufflebeam (SM)

Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02129, USA.

Mark P Ottensmeyer (MP)

Medical Device & Simulation Laboratory, Massachusetts General Hospital, Harvard Medical School, Cambridge, MA 02139, USA.

Gianluca De Novi (G)

Medical Device & Simulation Laboratory, Massachusetts General Hospital, Harvard Medical School, Cambridge, MA 02139, USA.

Christos Papadelis (C)

Bioengineering Department, The University of Texas at Arlington, Arlington, TX 76019, USA.
Neuroscience Research Center, Jane and John Justin Institute for Mind Health, Cook Children's Health Care System, Fort Worth, TX 76104, USA.

George Alexandrakis (G)

Bioengineering Department, The University of Texas at Arlington, Arlington, TX 76019, USA.

Classifications MeSH