Journal
PAIN
Volume 154, Issue 10, Pages 2160-2168Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.pain.2013.06.044
Keywords
DTI; Prediction; Chronic pain; Brain; Connectivity
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Funding
- National Institutes of Health, National Institute of Neurological Disorders and Stroke [NS035115]
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Neural mechanisms mediating the transition from acute to chronic pain remain largely unknown. In a longitudinal brain imaging study, we followed up patients with a single sub-acute back pain (SBP) episode for more than 1 year as their pain recovered (SBPr), or persisted (SBPp) representing a transition to chronic pain. We discovered brain white matter structural abnormalities (n = 24 SBP patients; SBPp = 12 and SBPr = 12), as measured by diffusion tensor imaging (DTI), at entry into the study in SBPp in comparison to SBPr. These white matter fractional anisotropy (FA) differences accurately predicted pain persistence over the next year, which was validated in a second cohort (n = 22 SBP patients; SBPp = 11 and SBPr = 11), and showed no further alterations over a 1-year period. Tractography analysis indicated that abnormal regional FA was linked to differential structural connectivity to medial vs lateral prefrontal cortex. Local FA was correlated with functional connectivity between medial prefrontal cortex and nucleus accumbens in SBPr. As we have earlier shown that the latter functional connectivity accurately predicts transition to chronic pain, we can conclude that brain structural differences, most likely existing before the back pain-inciting event and independent of the back pain, predispose subjects to pain chronification. (C) 2013 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
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