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

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By A Kuchinad • www.ProHealth.com • April 13, 2007


Journal: The Journal of Neuroscience. 2007 Apr 11;27(15):4004-4007.

Authors and affiliation: Kuchinad A, Schweinhardt P, Seminowicz DA, Wood PB, Chizh BA, Bushnell MC. McGill Centre for Research on Pain, Department of Neurology and Neurosurgery, and Department of Anesthesia and Faculty of Dentistry, McGill University, Montreal, Quebec, Canada; GlaxoSmithKline, Addenbrooke's Centre for Clinical Investigation, Addenbrooke's Hospital, Cambridge, UK. [E-mail: Catherine.bushnell@mcgill.ca ]

PMID: 17428976

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 (central nervous system) 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.





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