Abstract

Coordinate based meta-analysis (CBMA) is used to find regions of consistent activation across fMRI and PET studies selected for their functional relevance to a hypothesis. Results are clusters of foci where multiple studies report in the same spatial region, indicating functional relevance. Contrast meta-analysis finds regions where there are consistent differences in activation pattern between two groups. The activation likelihood estimate methods tackle these problems, but require a specification of uncertainty in foci location: the full width half max (FWHM). Results are sensitive to FWHM. Furthermore, contrast meta-analysis requires correction for multiple statistical tests. Consequently it is sensitive only to very significant localised differences that produce very small p-values, which remain significant after correction; subtle diffuse differences between the groups can be overlooked. In this report we redefine the FWHM parameter, by analogy with a density clustering algorithm, and provide a method to estimate it. The FWHM is modified to account for the number of studies in the analysis, and represents a substantial change to the CBMA philosophy that can be applied to the current algorithms. Consequently we observe more reliable detection of clusters when there are few studies in the CBMA, and a decreasing false positive rate with larger study numbers. By contrast the standard definition (FWHM independent of the number of studies) is demonstrated to paradoxically increase the false positive rate as the number of studies increases, while reducing ability to detect true clusters for small numbers of studies. We also provide an algorithm for contrast meta-analysis, which includes a correction for multiple correlated tests that controls for the proportion of false clusters expected under the null hypothesis. Furthermore, we detail an omnibus test of difference between groups that is more sensitive than contrast meta-analysis when differences are diffuse. This test is useful where contrast meta-analysis is unrevealing.

Highlights

  • A very popular method of performing a meta-analysis (MA) of functional magnetic resonance imaging and positron emission tomography (PET) data is coordinate based meta-analysis (CBMA)

  • We focus on the activation likelihood estimate (ALE) based method, which is possibly the most widely known of the CBMA schemes

  • By analogy with density clustering, we have redefined the full width half max (FWHM) parameter used in CBMA as a cluster density parameter, which depends on the cube root number of studies in the analysis, and is based on the idea that the results of CBMA should be commensurate when performed with different numbers of studies

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Summary

Introduction

A very popular method of performing a meta-analysis (MA) of functional magnetic resonance imaging (fMRI) and positron emission tomography (PET) data is coordinate based meta-analysis (CBMA). There are various approaches [1,2,3,4,5,6,7,8,9,10], but the common aim is to locate regions where different studies agree on the location of activation peaks (foci) better than expected by chance alone. The ALE method models the uncertainty of the reported foci using a Gaussian function with specified full width half max (FWHM) [1]. It estimates the likelihood, at each voxel, that there is consistent activation across multiple studies.

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