The practical use of realistic models in bioelectromagnetism is limited by
the time-consuming amount of numerical calculations. We propose a method le
ading to much higher speed than currently available, and compatible with an
y kind of numerical methods (boundary elements (BEM), finite elements, fini
te differences). Illustrated with the BEM for EEG and MEG, it applies to EC
G and MCG as well. The principle is two-fold. First, a Lead-Field matrix is
calculated (once for all) for a grid of dipoles covering the brain volume.
Second, any forward solution is interpolated from the pre-calculated Lead-
Fields corresponding to grid dipoles near the source. Extrapolation is used
for shallow sources falling outside the grid. Three interpolation techniqu
es were tested: trilinear, second-order Bezier (Bernstein polynomials), and
3D spline. The trilinear interpolation yielded the highest speed gain, wit
h factors better than x 10,000 for a 9,000-triangle BEM model. More accurat
e results could be obtained with the Bezier interpolation (speed gain simil
ar to1,000), which, combined with a 8-mm step grid, lead to intrinsic local
ization and orientation errors of only 0.2 mm and 0.2 degrees. Further impr
ovements in MEG could be obtained by interpolating only the contribution of
secondary currents. Cropping grids by removing shallow points lead to a mu
ch better estimation of the dipole orientation in EEG than when solving the
forward problem classically, providing an efficient alternative to locally
refined models. This method would show special usefulness when combining r
ealistic models with stochastic inverse procedures (simulated annealing, ge
netic algorithms) requiring many forward calculations. Hum, Brain Mapping 1
4:48-63, 2001. (C) 2001 Wiley-Liss, Inc.