15
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Accelerated Brain Gray Matter Loss in Fibromyalgia Patients: Premature Aging of the Brain?

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Fibromyalgia is an intractable widespread pain disorder that is most frequently diagnosed in women. It has traditionally been classified as either a musculoskeletal disease or a psychological disorder. Accumulating evidence now suggests that fibromyalgia may be associated with CNS dysfunction. In this study, we investigate anatomical changes in the brain associated with fibromyalgia. Using voxel-based morphometric analysis of magnetic resonance brain images, we examined the brains of 10 female fibromyalgia patients and 10 healthy controls. We found that fibromyalgia patients had significantly less total gray matter volume and showed a 3.3 times greater age-associated decrease in gray matter than healthy controls. The longer the individuals had had fibromyalgia, the greater the gray matter loss, with each year of fibromyalgia being equivalent to 9.5 times the loss in normal aging. In addition, fibromyalgia patients demonstrated significantly less gray matter density than healthy controls in several brain regions, including the cingulate, insular and medial frontal cortices, and parahippocampal gyri. The neuroanatomical changes that we see in fibromyalgia patients contribute additional evidence of CNS involvement in fibromyalgia. In particular, fibromyalgia appears to be associated with an acceleration of age-related changes in the very substance of the brain. Moreover, the regions in which we demonstrate objective changes may be functionally linked to core features of the disorder including affective disturbances and chronic widespread pain.

          Related collections

          Author and article information

          Journal
          J Neurosci
          J. Neurosci
          jneurosci
          J. Neurosci
          The Journal of Neuroscience
          Society for Neuroscience
          0270-6474
          1529-2401
          11 April 2007
          : 27
          : 15
          : 4004-4007
          Affiliations
          [1] 1McGill Centre for Research on Pain,
          [2] 2Department of Neurology and Neurosurgery, and
          [3] 3Department of Anesthesia and Faculty of Dentistry, McGill University, Montreal, Quebec, Canada H3A 2B2, and
          [4] 4GlaxoSmithKline, Addenbrooke's Centre for Clinical Investigation, Addenbrooke's Hospital, Cambridge CB2 2GG, United Kingdom
          Author notes
          Correspondence should be addressed to M. Catherine Bushnell, McGill Centre for Research on Pain, 3640 University Street, Room M19, Montreal, Quebec, Canada H3A 2B2. Catherine.bushnell@ 123456mcgill.ca
          Article
          PMC6672521 PMC6672521 6672521 3206465
          10.1523/JNEUROSCI.0098-07.2007
          6672521
          17428976
          14e26e7b-d5b2-4bf7-bb30-6b75a672de15
          Copyright © 2007 Society for Neuroscience 0270-6474/07/274004-04$15.00/0
          History
          : 9 January 2007
          : 21 February 2007
          : 2 March 2007
          Categories
          Articles
          Brief Communications
          Custom metadata

          aging,voxel-based morphometry,functional disorders,brain anatomy,pain,fibromyalgia

          Comments

          Comment on this article