Classification and characterisation of brain network changes in chronic back pain: A multicenter study

• Published in: Wellcome open research Vol. 3; p. 19
• Main Authors: Mano, Hiroaki, Kotecha, Gopal, Leibnitz, Kenji, Matsubara, Takashi, Nakae, Aya, Shenker, Nicholas, Shibata, Masahiko, Voon, Valerie, Yoshida, Wako, Lee, Michael, Yanagida, Toshio, Kawato, Mitsuo, Rosa, Maria Joao, Seymour, Ben
• Format: Journal Article
• Language: English
• Published: England Wellcome Trust Limited 2018; F1000 Research Limited; Wellcome
• Subjects: Adults; Arthritis; Artificial intelligence; Back pain; Biomarkers; Brain research; Chronic pain; Classification; Communications technology; Funding; Methods; Roles; Software; University colleges; Visualization; Writing; United Kingdom > UK; United States > US; Japan; Nociception; deep learning; arthritis; hub disruption; graph theory; multislice modularity; osteoarthritis; sensorimotor; Chronic pain; Connectomics
• ISSN: 2398-502X; 2398-502X
• DOI: 10.12688/wellcomeopenres.14069.2

Chronic pain is a common, often disabling condition thought to involve a combination of peripheral and central neurobiological factors. However, the extent and nature of changes in the brain is poorly understood. We investigated brain network architecture using resting-state fMRI data in chronic back pain patients in the UK and Japan (41 patients, 56 controls), as well as open data from USA. We applied machine learning and deep learning (conditional variational autoencoder architecture) methods to explore classification of patients/controls based on network connectivity. We then studied the network topology of the data, and developed a multislice modularity method to look for consensus evidence of modular reorganisation in chronic back pain. Machine learning and deep learning allowed reliable classification of patients in a third, independent open data set with an accuracy of 63%, with 68% in cross validation of all data. We identified robust evidence of network hub disruption in chronic pain, most consistently with respect to clustering coefficient and betweenness centrality. We found a consensus pattern of modular reorganisation involving extensive, bilateral regions of sensorimotor cortex, and characterised primarily by negative reorganisation - a tendency for sensorimotor cortex nodes to be less inclined to form pairwise modular links with other brain nodes. In contrast, intraparietal sulcus displayed a propensity towards positive modular reorganisation, suggesting that it might have a role in forming modules associated with the chronic pain state. The results provide evidence of consistent and characteristic brain network changes in chronic pain, characterised primarily by extensive reorganisation of the network architecture of the sensorimotor cortex.