Although much has been learned about the functional, organization of the hu
man brain through lesion-deficit analysis, the variety of statistical and i
mage-processing methods developed for this purpose precludes a closed-form
analysis of the statistical power of these systems. Therefore, we developed
a lesion-deficit simulator (LDS), which generates artificial subjects, eac
h of which consists of a set of functional deficits, and a brain image with
lesions; the deficits and lesions conform to predefined distributions. We
used probability distributions to model the number, sizes, and spatial dist
ribution of lesions, to model the structure-function associations, and to m
odel registration error. We used the LDS to evaluate, as examples, the effe
cts of the complexities and strengths of lesion-deficit associations, and o
f registration error, on the power of lesion-deficit analysis. We measured
the numbers of recovered associations from these simulated data, as a funct
ion of the number of subjects analyzed, the strengths and number of associa
tions in the statistical model, the number of structures associated with a
particular function, and the prior probabilities of structures being abnorm
al. The number of subjects required to recover the simulated lesion-deficit
associations was found to have an inverse relationship to the strength of
associations, and to the smallest probability in the structure-function mod
el. The number of structures associated with a particular function (i.e., t
he complexity of associations) had a much greater effect on the performance
of the analysis method than did the total number of associations. We also
found that registration error of 5 mm or less reduces the number of associa
tions discovered by approximately 13% compared to perfect registration. The
LDS provides a flexible framework for evaluating many aspects of lesion-de
ficit analysis. (C) 2000 Wiley-Liss, Inc.