Abstract

Several studies have attempted to characterize morphological brain changes due to chronic pain. Although it has repeatedly been suggested that longstanding pain induces gray matter modifications, there is still some controversy surrounding the direction of the change (increase or decrease in gray matter) and the role of psychological and psychiatric comorbidities. In this study, we propose a novel, network-oriented, meta-analytic approach to characterize morphological changes in chronic pain. We used network decomposition to investigate whether different kinds of chronic pain are associated with a common or specific set of altered networks. Representational similarity techniques, network decomposition and model-based clustering were employed: i) to verify the presence of a core set of brain areas commonly modified by chronic pain; ii) to investigate the involvement of these areas in a large-scale network perspective; iii) to study the relationship between altered networks and; iv) to find out whether chronic pain targets clusters of areas. Our results showed that chronic pain causes both core and pathology-specific gray matter alterations in large-scale networks. Common alterations were observed in the prefrontal regions, in the anterior insula, cingulate cortex, basal ganglia, thalamus, periaqueductal gray, post- and pre-central gyri and inferior parietal lobule. We observed that the salience and attentional networks were targeted in a very similar way by different chronic pain pathologies. Conversely, alterations in the sensorimotor and attention circuits were differentially targeted by chronic pain pathologies. Moreover, model-based clustering revealed that chronic pain, in line with some neurodegenerative diseases, selectively targets some large-scale brain networks. Altogether these findings indicate that chronic pain can be better conceived and studied in a network perspective.

Highlights

  • Studies using voxel-based morphometry (VBM), a computationalbased technique that measures focal differences in concentrationsChronic pain is defined by the International Association for the of brain tissue using a voxel-wise comparison between two groupsStudy of Pain as a pain persisting over the healing phase of an injury of subjects (Ashburner and Friston, 2000), have reported conflicting (Loeser and Treede, 2008)

  • The Anatomical likelihood estimation (ALE) results showed that chronic pain is associated with a common core set of gray matter decreases in the bilateral medial frontal gyri, bilateral superior frontal gyri, right pre- and post-central gyri, bilateral insula, right cingulate cortex, basal ganglia, thalamus and periaqueductal gray

  • This study was designed to: i) verify the presence of a core set of brain areas commonly modified by chronic pain; ii) investigate the involvement of these areas in a large-scale network perspective; iii) study the relationship between altered networks and; iv) find out whether chronic pain targets clusters of areas

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Summary

Introduction

Studies using voxel-based morphometry (VBM), a computationalbased technique that measures focal differences in concentrationsChronic pain is defined by the International Association for the of brain tissue using a voxel-wise comparison between two groupsStudy of Pain as a pain persisting over the healing phase of an injury of subjects (Ashburner and Friston, 2000), have reported conflicting (Loeser and Treede, 2008). F. Cauda et al / NeuroImage: Clinical 4 (2014) 676–686 change (Hsu et al, 2009; Rocca et al, 2006; Schmidt-Wilcke et al, 2005; Schmidt-Wilcke et al, 2007) in gray matter volume or density. Cauda et al / NeuroImage: Clinical 4 (2014) 676–686 change (Hsu et al, 2009; Rocca et al, 2006; Schmidt-Wilcke et al, 2005; Schmidt-Wilcke et al, 2007) in gray matter volume or density These discrepancies may be underpinned by the different category of chronic pain considered (e.g. low back pain or migraine), by the different underlying etiology (e.g. nociceptive vs neuropathic) or by other confounding factors such as, for example, concomitant psychiatric comorbidities like depression or anxiety. We addressed three questions: i) is there a core set of brain areas altered in chronic pain?; ii) are different kinds of chronic pain associated with a common or specific set of altered large-scale brain networks?; and iii) when alterations of gray matter are reported together, do they reflect clusters of modified areas that share some relationship or are they casually found together?

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