bioRxivNeurosciencePreprint
Small effect size leads to reproducibility failure in resting-state fMRI studies
Xize JiaiD, Na ZhaoiD, Barek Barton, Roxana Gabriela BurciuiD, Nicolas CarrièreiD, Antonio CerasaiD, Boyu CheniD, Jun CheniD, Stephen A. CoombesiD, Luc DefebvreiD, Christine Delmaire, Kathy DujardiniD, Fabrizio EspositoiD, Guoguang FaniD, Federica Di NardoiD, Yi-Xuan Feng, Brett W. FlingiD, Saurabh Garg, Moran GilatiD, Martin GorgesiD, Shu‐Leong HoiD, Fay Bahling HorakiD, Xiao HuiD, Xiaofei HuiD, Biao HuangiD, , Yu‐Feng ZangiD
Abstract
Thousands of papers using resting-state functional magnetic resonance imaging (RS-fMRI) have been published on brain disorders. Results in each paper may have survived correction for multiple comparison. However, since there have been no robust results from large scale meta-analysis, we do not know how many of published results are truly positives. The present meta-analytic work included 60 original studies, with 57 studies (4 datasets, 2266 participants) that used a between-group design and 3 studies (1 dataset, 107 participants) that employed a within-group design. To evaluate the effect size of brain disorders, a very large neuroimaging dataset ranging from neurological to psychiatric isorders together with healthy individuals have been analyzed. Parkinsons disease off levodopa (PD-off) included 687 participants from 15 studies. PD on levodopa (PD-on) included 261 participants from 9 studies. Autism spectrum disorder (ASD) included 958 participants from 27 studies. The meta-analyses of a metric named amplitude of low frequency fluctuation (ALFF) showed that the effect size (Hedges g) was 0.19 - 0.39 for the 4 datasets using between-group design and 0.46 for the dataset using within-group design. The effect size of PD-off, PD-on and ASD were 0.23, 0.39, and 0.19, respectively. Using the meta-analysis results as the robust results, the between-group design results of each study showed high false negative rates (median 99%), high false discovery rates (median 86%), and low accuracy (median 1%), regardless of whether stringent or liberal multiple comparison correction was used. The findings were similar for 4 RS-fMRI metrics including ALFF, regional homogeneity, and degree centrality, as well as for another widely used RS-fMRI metric namely seed-based functional connectivity. These observations suggest that multiple comparison correction does not control for false discoveries across multiple studies when the effect sizes are relatively small. Meta-analysis on un-thresholded t-maps is critical for the recovery of ground truth. We recommend that to achieve high reproducibility through meta-analysis, the neuroimaging research field should share raw data or, at minimum, provide un-thresholded statistical images.
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