• Chelsea M Kaplan, Andrew Schrepf, Ishtiaq Mawla, Eric Ichesco, Kevin F Boehnke, Adriene Beltz, Emily Foxen-Craft, Michael P Puglia, Alexandre Tsodikov, David A Williams, Afton L Hassett, Daniel J Clauw, Steven E Harte, and Richard E Harris.
• Department of Anesthesiology, University of Michigan Medical School, Ann Arbor, MI, United States.
• Pain. 2022 Apr 1; 163 (4): e596e603e596-e603.

AbstractAltered brain structure and function is evident in adults with multisite chronic pain. Although many such adults trace their pain back to childhood, it has been difficult to disentangle whether central nervous system alterations precede or are consequences of chronic pain. If the former is true, aberrant brain activity may identify children vulnerable to developing chronic pain later in life. We examined structural and functional brain magnetic resonance imaging metrics in a subset of children from the first 2 assessments of the Adolescent Brain and Cognitive Development Study. Children (aged 9-10) who were pain free at baseline and then developed multisite pain 1 year later (n = 115) were matched to control children who were pain free at both timepoints (n = 230). We analyzed brain structure (cortical thickness and gray matter volume) and function (spontaneous neural activity and functional connectivity). Results were deemed significant at the cluster level P < 0.05 false discovery rate corrected for multiple comparisons. At baseline, children who subsequently developed multisite pain had increased neural activity in superior parietal /primary somatosensory and motor cortices and decreased activity in the medial prefrontal cortex. They also exhibited stronger functional connectivity between the salience network, somatosensory, and default mode network regions. No significant differences in the brain structure were observed. Increased neural activity and functional connectivity between brain regions, consistent to that seen in adults with chronic pain, exist in children before developing multisite pain. These findings may represent a neural vulnerability to developing future chronic pain.Copyright © 2021 International Association for the Study of Pain.

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