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      Decrease of Gray Matter Volume in the Midbrain is Associated with Treatment Response in Medication-Overuse Headache: Possible Influence of Orbitofrontal Cortex

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          Abstract

          Patients with chronic daily headache and overuse of analgesics, triptans, or other acute headache compounds, are considered to suffer from medication-overuse headache (MOH). This implies that medication overuse is the cause of headache chronification. It remains a key question why only two-thirds of patients with chronic migraine-like headache and overuse of pain medication improve after detoxification, whereas the remainder continue to have chronic headache. In the present longitudinal MRI study, we used voxel-based morphometry to investigate gray matter changes related to medication withdrawal in a group of humans with MOH. As a main result, we found that only patients with significant clinical improvement showed a significant decrease of previously increased gray matter in the midbrain including periaqueductal gray matter and nucleus cuneiformis, whereas patients without improvement did not. Patients without treatment response had less gray matter in the orbitofrontal cortex. Another striking result is the correlation of treatment response with the amount of orbitofrontal gray matter. Thus, we demonstrate adaptive gray matter changes within the pain modulatory system in patients with MOH who responded to detoxification, probably reflecting neuronal plasticity. Decreased gray matter in the orbitofrontal cortex at baseline may be predictive of poor response to treatment.

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          Author and article information

          Journal
          J Neurosci
          J. Neurosci
          jneuro
          jneurosci
          J. Neurosci
          The Journal of Neuroscience
          Society for Neuroscience
          0270-6474
          1529-2401
          25 September 2013
          : 33
          : 39
          : 15343-15349
          Affiliations
          [1] 1Department of Neurology, University Hospital Zurich, CH-8091 Zurich, Switzerland,
          [2] 2Institute for Biomedical Engineering, Swiss Federal Institute of Technology and the University of Zurich, CH-8091 Zurich, Switzerland,
          [3] 3Institute of Neuroradiology, University Hospital Zurich, CH-8091 Zurich, Switzerland, and
          [4] 4Rehaclinic Bad Zurzach, CH-5330 Bad Zurzach, Switzerland
          Author notes
          Correspondence should be addressed to Peter S. Sándor, Rehaclinic Bad Zurzach, Quellenstrasse 34, CH-5330 Bad Zurzach, Switzerland. peter.sandor@ 123456ksb.ch

          Author contributions: F.R. and P.S.S. designed research; F.R., A.R.G., M.M., and R.L. performed research; R.L. and S.K. contributed unpublished reagents/analytic tools; F.R. and M.M. analyzed data; F.R., S.K., and P.S.S. wrote the paper.

          Article
          PMC6618461 PMC6618461 6618461 3804-12
          10.1523/JNEUROSCI.3804-12.2013
          6618461
          24068801
          df9dfe7a-58b8-4a84-8318-4f29c19673cb
          Copyright © 2013 the authors 0270-6474/13/3315343-07$15.00/0
          History
          : 9 August 2012
          : 11 July 2013
          : 12 July 2013
          Categories
          Articles
          Development/Plasticity/Repair

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