Group-ICA model order highlights patterns of functional brain connectivity

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Abstract

Resting-state networks (RSNs) can be reliably and reproducibly detected using independent component analysis (ICA) at both individual subject and group levels. Altering ICA dimensionality (model order) estimation can have a significant impact on the spatial characteristics of the RSNs as well as their parcellation into sub-networks. Recent evidence from several neuroimaging studies suggests that the human brain has a modular hierarchical organization which resembles the hierarchy depicted by different ICA model orders. We hypothesized that functional connectivity between-group differences measured with ICA might be affected by model order selection. We investigated differences in functional connectivity using so-called dual regression as a function of ICA model order in a group of unmedicated seasonal affective disorder (SAD) patients compared to normal healthy controls. The results showed that the detected disease-related differences in functional connectivity alter as a function of ICA model order. The volume of between-group differences altered significantly as a function of ICA model order reaching maximum at model order 70 (which seems to be an optimal point that conveys the largest between-group difference) then stabilized afterwards. Our results show that fine-grained RSNs enable better detection of detailed disease-related functional connectivity changes. However, high model orders show an increased risk of false positives that needs to be overcome. Our findings suggest that multilevel ICA exploration of functional connectivity enables optimization of sensitivity to brain disorders. © 2011 Abou Elseoud, Littow, Remes, Starck, Nikkinen, Nissilä, Timonen, Tervonen and Kiviniemi.

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APA

Elseoud, A. A., Littow, H., Remes, J., Starck, T., Nikkinen, J., Nissilä, J., … Kiviniemi, V. (2011). Group-ICA model order highlights patterns of functional brain connectivity. Frontiers in Systems Neuroscience, (JUNE 2011). https://doi.org/10.3389/fnsys.2011.00037

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