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Topologically Reorganized Connectivity Architecture of Default-Mode, Executive-Control, and Salience Networks Across Working Memory Task Loads

Overview
Journal Cereb Cortex
Specialty Neurology
Date 2015 Jan 18
PMID 25596593
Citations 111
Authors
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Abstract

The human brain is topologically organized into a set of spatially distributed, functionally specific networks. Of these networks, the default-mode network (DMN), executive-control network (ECN), and salience network (SN) have received the most attention recently for their vital roles in cognitive functions. However, very little is known about whether and how the interactions within and between these 3 networks would be modulated by cognitive demands. Here, we employed graph-based modularity analysis to identify the DMN, ECN, and SN during an N-back working memory (WM) task and further investigated the modulation of intra- and inter-network interactions at different cognitive loads. As the task load elevated, functional connectivity decreased within the DMN while increased within the ECN, and the SN connected more with both the DMN and ECN. Within-network connectivity of the ventral and dorsal posterior cingulate cortex was differentially modulated by cognitive load. Further, the superior parietal regions in the ECN showed increased internetwork connections at higher WM loads, and these increases correlated positively with WM task performance. Together, these findings advance our understanding of dynamic integrations of specialized brain systems in response to cognitive demands and may serve as a baseline for assessing potential disruptions of these interactions in pathological conditions.

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References
1.
Vogt B, Vogt L, Laureys S . Cytology and functionally correlated circuits of human posterior cingulate areas. Neuroimage. 2005; 29(2):452-66. PMC: 2649771. DOI: 10.1016/j.neuroimage.2005.07.048. View

2.
Leech R, Braga R, Sharp D . Echoes of the brain within the posterior cingulate cortex. J Neurosci. 2012; 32(1):215-22. PMC: 6621313. DOI: 10.1523/JNEUROSCI.3689-11.2012. View

3.
Kitzbichler M, Henson R, Smith M, Nathan P, Bullmore E . Cognitive effort drives workspace configuration of human brain functional networks. J Neurosci. 2011; 31(22):8259-70. PMC: 6622866. DOI: 10.1523/JNEUROSCI.0440-11.2011. View

4.
Honey G, Fu C, Kim J, Brammer M, Croudace T, Suckling J . Effects of verbal working memory load on corticocortical connectivity modeled by path analysis of functional magnetic resonance imaging data. Neuroimage. 2002; 17(2):573-82. View

5.
Wager T, Smith E . Neuroimaging studies of working memory: a meta-analysis. Cogn Affect Behav Neurosci. 2004; 3(4):255-74. DOI: 10.3758/cabn.3.4.255. View