• Florence B Pomares, Thomas Funck, Natasha A Feier, Steven Roy, Alexandre Daigle-Martel, Marta Ceko, Sridar Narayanan, David Araujo, Alexander Thiel, Nikola Stikov, Mary-Ann Fitzcharles, and Petra Schweinhardt.
• Alan Edwards Centre for Research on Pain, McGill University, Montreal, Quebec H3A 0C7, Canada, florence.pomares@gmail.com.
• J. Neurosci. 2017 Feb 1; 37 (5): 1090-1101.

AbstractChronic pain patients present with cortical gray matter alterations, observed with anatomical magnetic resonance (MR) imaging. Reduced regional gray matter volumes are often interpreted to reflect neurodegeneration, but studies investigating the cellular origin of gray matter changes are lacking. We used multimodal imaging to compare 26 postmenopausal women with fibromyalgia with 25 healthy controls (age range: 50-75 years) to test whether regional gray matter volume decreases in chronic pain are associated with compromised neuronal integrity. Regional gray matter decreases were largely explained by T1 relaxation times in gray matter, a surrogate measure of water content, and not to any substantial degree by GABAA receptor concentration, an indirect marker of neuronal integrity measured with [18F] flumazenil PET. In addition, the MR spectroscopy marker of neuronal viability, N-acetylaspartate, did not differ between patients and controls. These findings suggest that decreased gray matter volumes are not explained by compromised neuronal integrity. Alternatively, a decrease in neuronal matter could be compensated for by an upregulation of GABAA receptors. The relation between regional gray matter and T1 relaxation times suggests decreased tissue water content underlying regional gray matter decreases. In contrast, regional gray matter increases were explained by GABAA receptor concentration in addition to T1 relaxation times, indicating perhaps increased neuronal matter or GABAA receptor upregulation and inflammatory edema. By providing information on the histological origins of cerebral gray matter alterations in fibromyalgia, this study advances the understanding of the neurobiology of chronic widespread pain.Copyright © 2017 the authors 0270-6474/17/371091-12$15.00/0.

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