This title appears in the Scientific Report : 2014 

Meta-analytic connectivity modelling revisited: Controlling for activation base rates
Langner, Robert (Corresponding Author)
Rottschy, C. / Laird, A. R. / Fox, P. T. / Eickhoff, Simon
Strukturelle und funktionelle Organisation des Gehirns; INM-1
NeuroImage, 99 (2014) S. 559-570
Orlando, Fla. Academic Press 2014
10.1016/j.neuroimage.2014.06.007
24945668
Journal Article
Theory, modelling and simulation
The Human Brain Project
Pathophysiological Mechanisms of Neurological and Psychiatric Diseases
Please use the identifier: http://dx.doi.org/10.1016/j.neuroimage.2014.06.007 in citations.
Co-activation of distinct brain regions is a measure of functional interaction, or connectivity, between those regions. The co-activation pattern of a given region can be investigated using seed-based activation likelihood estimation meta-analysis of functional neuroimaging data stored in databases such as BrainMap. This method reveals inter-regional functional connectivity by determining brain regions that are consistently co-activated with a given region of interest (the “seed”) across a broad range of experiments. In current implementations of this meta-analytic connectivity modeling (MACM), significant spatial convergence (i.e. consistent co-activation) is distinguished from noise by comparing it against an unbiased null-distribution of random spatial associations between experiments according to which all gray-matter voxels have the same chance of convergence. As the a priori probability of finding activation in different voxels markedly differs across the brain, computing such a quasi-rectangular null-distribution renders the detection of significant convergence more likely in those voxels that are frequently activated. Here, we propose and test a modified MACM approach that takes this activation frequency bias into account. In this new specific co-activation likelihood estimation (SCALE) algorithm, a null-distribution is generated that reflects the base rate of reporting activation in any given voxel and thus equalizes the a priori chance of finding across-study convergence in each voxel of the brain. Using four exemplary seed regions (right visual area V4, left anterior insula, right intraparietal sulcus, and subgenual cingulum), our tests corroborated the enhanced specificity of the modified algorithm, indicating that SCALE may be especially useful for delineating distinct core networks of co-activation.