R01MH130490
Project Grant
Overview
Grant Description
Charge-Based Brain Modeling Engine with Boundary Element Fast Multipole Method - Abstract
All major open-source brain modeling packages currently available (e.g., SimNIBS, Duneuro, SCIRun, ROAST) as well as their commercial counterparts (e.g., Sim4Life, ANSYS Maxwell, COMSOL) use the electric potential-based finite element method (FEM) for electromagnetic modeling. FEM has been continuously improved over the past 60 years, is simple to implement, and can model averaged tissue anisotropy.
At the same time, FEM may have some intrinsic weaknesses specifically affecting high-definition brain modeling. The present proposal aims to develop and disseminate a novel alternative brain modeling engine. In contrast to FEM which uses the electric potential, it operates with the primary (bio)physical quantity – surface (and volumetric) induced electric charge density. To model charge interactions, it naturally employs the modern fast multipole method (FMM) instead of FEM.
For piecewise homogeneous biological media of any complexity, only surface charges at boundaries are present. Their interactions are most accurately described by the boundary element method (BEM). This combination of BEM and FMM is the new proposed BEM-FMM charge engine. The principal advantage of BEM-FMM is its numerically unconstrained spatial field resolution.
Aim 1. Improve and complete the BEM-FMM modeling engine. Sub-aims: (i) Major speed up of the BEM-FMM engine; (ii) New adaptive mesh refinement algorithm; (iii) New volumetric anisotropic co-solver; (iv) Computing activating function with unconstrained numerical resolution; and (v) Full-scale numerical verification against established FEM solvers SimNIBS and Duneuro at meso (submillimeter) scale.
Aim 2. BEM-FMM testbed for non-invasive recordings and stimulation.
2A. Develop BEM-FMM source localization stream for EEG/MEG recordings. We will construct and validate an improvement over currently existing BEM EEG/MEG source localization software suites using BEM-FMM. We will deliver a ready-to-use testbed with twenty head models and EEG/MEG experimental data.
2B. Develop a BEM-FMM modeling stream with extracerebral compartments for noninvasive stimulation. For enhanced resolution, we will automatically add fine-resolution major extracerebral compartments into existing segmentation pipelines based on anatomical rules. We will then deliver the ready-to-use BEM-FMM testbed targeting TES and ECT (electroconvulsive therapy) where their effect might be critical for the correct dosage prediction and correct targeting.
Aim 3. BEM-FMM testbed for invasive electrical stimulation.
3A. Validate BEM-FMM testbed for modeling activating function in animal axons. Verification for a giant interneuronal axon of crayfish Procambarus clarkia via electrical/magnetic stimulation and compound action potential generation for parallel fibers in turtle Pseudemys scripta elegans cerebellum will be done.
3B. Verify BEM-FMM testbed for modeling DBS responses. Using retrospective clinical data, we will develop a BEM-FMM algorithm for patient-specific multipolar DBS and evaluate whether the model predictions align with clinical observations.
All major open-source brain modeling packages currently available (e.g., SimNIBS, Duneuro, SCIRun, ROAST) as well as their commercial counterparts (e.g., Sim4Life, ANSYS Maxwell, COMSOL) use the electric potential-based finite element method (FEM) for electromagnetic modeling. FEM has been continuously improved over the past 60 years, is simple to implement, and can model averaged tissue anisotropy.
At the same time, FEM may have some intrinsic weaknesses specifically affecting high-definition brain modeling. The present proposal aims to develop and disseminate a novel alternative brain modeling engine. In contrast to FEM which uses the electric potential, it operates with the primary (bio)physical quantity – surface (and volumetric) induced electric charge density. To model charge interactions, it naturally employs the modern fast multipole method (FMM) instead of FEM.
For piecewise homogeneous biological media of any complexity, only surface charges at boundaries are present. Their interactions are most accurately described by the boundary element method (BEM). This combination of BEM and FMM is the new proposed BEM-FMM charge engine. The principal advantage of BEM-FMM is its numerically unconstrained spatial field resolution.
Aim 1. Improve and complete the BEM-FMM modeling engine. Sub-aims: (i) Major speed up of the BEM-FMM engine; (ii) New adaptive mesh refinement algorithm; (iii) New volumetric anisotropic co-solver; (iv) Computing activating function with unconstrained numerical resolution; and (v) Full-scale numerical verification against established FEM solvers SimNIBS and Duneuro at meso (submillimeter) scale.
Aim 2. BEM-FMM testbed for non-invasive recordings and stimulation.
2A. Develop BEM-FMM source localization stream for EEG/MEG recordings. We will construct and validate an improvement over currently existing BEM EEG/MEG source localization software suites using BEM-FMM. We will deliver a ready-to-use testbed with twenty head models and EEG/MEG experimental data.
2B. Develop a BEM-FMM modeling stream with extracerebral compartments for noninvasive stimulation. For enhanced resolution, we will automatically add fine-resolution major extracerebral compartments into existing segmentation pipelines based on anatomical rules. We will then deliver the ready-to-use BEM-FMM testbed targeting TES and ECT (electroconvulsive therapy) where their effect might be critical for the correct dosage prediction and correct targeting.
Aim 3. BEM-FMM testbed for invasive electrical stimulation.
3A. Validate BEM-FMM testbed for modeling activating function in animal axons. Verification for a giant interneuronal axon of crayfish Procambarus clarkia via electrical/magnetic stimulation and compound action potential generation for parallel fibers in turtle Pseudemys scripta elegans cerebellum will be done.
3B. Verify BEM-FMM testbed for modeling DBS responses. Using retrospective clinical data, we will develop a BEM-FMM algorithm for patient-specific multipolar DBS and evaluate whether the model predictions align with clinical observations.
Awardee
Funding Goals
NOT APPLICABLE
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Worcester,
Massachusetts
016092247
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the End Date has been shortened from 05/31/28 to 05/31/27 and the total obligations have increased 328% from $768,752 to $3,293,288.
Worcester Polytechnic Institute was awarded
Advanced Brain Modeling Engine: BEM-FMM High-Resolution Neurostimulation
Project Grant R01MH130490
worth $3,293,288
from the National Institute of Mental Health in July 2023 with work to be completed primarily in Worcester Massachusetts United States.
The grant
has a duration of 3 years 10 months and
was awarded through assistance program 93.242 Mental Health Research Grants.
The Project Grant was awarded through grant opportunity Competing Revisions to Existing NIH Single Project Research Grants and Cooperative Agreements (Clinical Trial Optional).
Status
(Ongoing)
Last Modified 7/6/26
Period of Performance
7/19/23
Start Date
5/31/27
End Date
Funding Split
$3.3M
Federal Obligation
$0.0
Non-Federal Obligation
$3.3M
Total Obligated
Activity Timeline
Subgrant Awards
Disclosed subgrants for R01MH130490
Transaction History
Modifications to R01MH130490
Additional Detail
Award ID FAIN
R01MH130490
SAI Number
R01MH130490-1707856038
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75N700 NIH National Institute of Mental Health
Funding Office
75N700 NIH National Institute of Mental Health
Awardee UEI
HJNQME41NBU4
Awardee CAGE
81359
Performance District
MA-02
Senators
Edward Markey
Elizabeth Warren
Elizabeth Warren
Budget Funding
| Federal Account | Budget Subfunction | Object Class | Total | Percentage |
|---|---|---|---|---|
| National Institute of Mental Health, National Institutes of Health, Health and Human Services (075-0892) | Health research and training | Grants, subsidies, and contributions (41.0) | $768,752 | 100% |
Modified: 7/6/26