Pain-Evoked Reorganization in Functional Brain Networks. (9th December 2019)

• Record Type: Journal Article
• Authors: Zheng, Weihao; Woo, Choong-Wan; Yao, Zhijun; Goldstein, Pavel; Atlas, Lauren Y; Roy, Mathieu; Schmidt, Liane; Krishnan, Anjali; Jepma, Marieke; Hu, Bin; Wager, Tor D
• Is Part Of: Cerebral cortex. Volume 30:Number 5(2020)
• Page Start: 2804
• Page End: 2822
• Publication Date: 2019-12-09
• Subjects: functional network -- hub disruption -- inter-system connectivity -- immediate pain -- reorganization; Cerebral cortex -- Periodicals; Brain -- Periodicals; 612.825
• DOI: 10.1093/cercor/bhz276
• Languages: English
• ISSNs: 1047-3211

Abstract

Abstract: Recent studies indicate that a significant reorganization of cerebral networks may occur in patients with chronic pain, but how immediate pain experience influences the organization of large-scale functional networks is not yet well characterized. To investigate this question, we used functional magnetic resonance imaging in 106 participants experiencing both noxious and innocuous heat. Painful stimulation caused network-level reorganization of cerebral connectivity that differed substantially from organization during innocuous stimulation and standard resting-state networks. Noxious stimuli increased somatosensory network connectivity with (a) frontoparietal networks involved in context representation, (b) "ventral attention network" regions involved in motivated action selection, and (c) basal ganglia and brainstem regions. This resulted in reduced "small-worldness, " modularity (fewer networks), and global network efficiency and in the emergence of an integrated "pain supersystem" (PS) whose activity predicted individual differences in pain sensitivity across 5 participant cohorts. Network hubs were reorganized ("hub disruption") so that more hubs were localized in PS, and there was a shift from "connector" hubs linking disparate networks to "provincial" hubs connecting regions within PS. Our findings suggest that pain reorganizes the network structure of large-scale brain systems. These changes may prioritize responses to painful events and provide nociceptive systems privileged access to central control of cognition and action during pain.