Impact of sample size and regression of tissue‐specific signals on effective connectivity within the core default mode network

Interactions within brain networks are inherently directional, which are inaccessible to classical functional connectivity estimates from resting‐state functional magnetic resonance imaging (fMRI) but can be detected using spectral dynamic causal modeling (DCM). The sample size and unavoidable prese...

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Bibliographic Details
Published inHuman brain mapping Vol. 44; no. 17; pp. 5858 - 5870
Main Authors Silchenko, Alexander N., Hoffstaedter, Felix, Eickhoff, Simon B.
Format Journal Article
LanguageEnglish
Published San Antonio John Wiley & Sons, Inc 01.12.2023
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Summary:Interactions within brain networks are inherently directional, which are inaccessible to classical functional connectivity estimates from resting‐state functional magnetic resonance imaging (fMRI) but can be detected using spectral dynamic causal modeling (DCM). The sample size and unavoidable presence of nuisance signals during fMRI measurement are the two important factors influencing the stability of group estimates of connectivity parameters. However, most recent studies exploring effective connectivity (EC) have been conducted with small sample sizes and minimally pre‐processed datasets. We explore the impact of these two factors by analyzing clean resting‐state fMRI data from 330 unrelated subjects from the Human Connectome Project database. We demonstrate that both the stability of the model selection procedures and the inference of connectivity parameters are highly dependent on the sample size. The minimum sample size required for stable DCM is approximately 50, which may explain the variability of the DCM results reported so far. We reveal a stable pattern of EC within the core default mode network computed for large sample sizes and demonstrate that the use of subject‐specific thresholded whole‐brain masks for tissue‐specific signals regression enhances the detection of weak connections.
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ISSN:1065-9471
1097-0193
1097-0193
DOI:10.1002/hbm.26481