The default mode network, long thought to be deactivated during focused tasks and to interfere with performance, may actually help fulfill cognitive demands. In a finger-tapping task with functional MRI, the network showed task-specific changes in its topography. Faster reaction times were predicted by stronger connectivity between the posterior cingulate cortex and the left superior frontal gyrus. The network's connections reconfigured dynamically during the task, maintaining efficient small-world organization while supporting higher-level parallel processing. These results suggest the default mode network does not disengage but may contribute to task-relevant processing.
Patterns of functional interactions across distributed brain regions are thought to provide a scaffold for conscious processing, with topological changes seen in loss of consciousness. Using resting-state fMRI in healthy participants at baseline and two levels of propofol-induced sedation, the study found a persistent modular brain architecture but significant reorganization of brain hubs that formed parts of a wider rich-club collective. Reduced strength of rich-club connectivity was significantly associated with poorer performance on a semantic judgment task, highlighting the importance of this higher-order topological feature for conscious cognition.