Journal
PAIN
Volume 154, Issue 1, Pages 24-33Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.pain.2012.07.029
Keywords
Resting state networks; Chronic low back pain; Functional magnetic resonance imaging; Psychophysics; Human
Categories
Funding
- National Institutes of Health [K23-DA020681, R01-AT004714, P01-AT002048, R01-AT 005280, R01-AT006146, P01-AT006663]
- NATIONAL CENTER FOR COMPLEMENTARY & ALTERNATIVE MEDICINE [R01AT005280, R01AT004714] Funding Source: NIH RePORTER
- NATIONAL CENTER FOR COMPLEMENTARY &ALTERNATIVE MEDICINE [P01AT002048] Funding Source: NIH RePORTER
- National Center for Complementary & Integrative Health [P01AT006663] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE ON DRUG ABUSE [K23DA020681] Funding Source: NIH RePORTER
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Neuroimaging studies have suggested the presence of alterations in the anatomo-functional properties of the brain of patients with chronic pain. However, investigation of the brain circuitry supporting the perception of clinical pain presents significant challenges, particularly when using traditional neuroimaging approaches. While potential neuroimaging markers for clinical pain have included resting brain connectivity, these cross-sectional studies have not examined sensitivity to within-subject exacerbation of pain. We used the dual regression probabilistic Independent Component Analysis approach to investigate resting-state connectivity on arterial spin labeling data. Brain connectivity was compared between patients with chronic low back pain (cLBP) and healthy controls, before and after the performance of maneuvers aimed at exacerbating clinical pain levels in the patients. Our analyses identified multiple resting state networks, including the default mode network (DMN). At baseline, patients demonstrated stronger DMN connectivity to the pregenual anterior cingulate cortex (pgACC), left inferior parietal lobule, and right insula (rINS). Patients' baseline clinical pain correlated positively with connectivity strength between the DMN and right insula (DMN-rINS). The performance of calibrated physical maneuvers induced changes in pain, which were paralleled by changes in DMN-rINS connectivity. Maneuvers also disrupted the DMN-pgACC connectivity, which at baseline was anticorrelated with pain. Finally, baseline DMN connectivity predicted maneuver-induced changes in both pain and DMN-rINS connectivity. Our results support the use of arterial spin labeling to evaluate clinical pain, and the use of resting DMN connectivity as a potential neuroimaging biomarker for chronic pain perception. (C) 2012 International Association for the Study of Pain. Published by Elsevier B. V. All rights reserved.
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