4.4 Article

Increased levels of Neurotrophins are not specific for chronic migraine: Evidence from primary fibromyalgia syndrome

Journal

JOURNAL OF PAIN
Volume 8, Issue 9, Pages 737-745

Publisher

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.jpain.2007.05.002

Keywords

nerve growth factor; brain-derived neurotrophic factor; glutamate; cerebrospinal fluid; chronic migraine; fibromyalgia

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All data obtained in experimental animal pain models support the role of nerve growth factor (NGF) as a putative candidate intervening in the pathogenesis of chronic pain, including chronic daily headache (CDH). Few studies have been carried out to establish its role in maintaining pain states in humans. The present study was aimed at investigating cerebrospinal fluid (CSF) levels of NGF and brain-derived neurotrophic factor (BDNF), both measured by sensitive immunoassay, in 20 chronic migraine (CM) patients and 20 patients affected by primary fibromyalgia syndrome (PFMS), compared with those of 20 age-matched control subjects. Significantly higher levels of both neurotrophins and glutamate were found. A significantly positive correlation emerged between CSF values of BDNF and those of NGF (r =.61, P <.001; r =.53, P <.01) and glutamate (r =.44, P <.02; r =.51, P <.01) in CM and PFMS patients, respectively. These findings suggest the possibility of a NGF-mediated up-regulation of BDNF involved in the pathophysiological events underlying long-term neuroplastic changes in persistent chronic painful conditions, such as CM and fibromyalgia. NGF might indirectly exert its effect through enhancing glutamatergic transmission via BDNF. The above mechanisms could account for sustained central sensitization in both chronic pain states. Perspective: This article presents findings of higher NGF and BDNF levels correlated to increased glutamate levels in the OF of both chronic migraine and fibromyalgia patients. This opens new insights into the pathogenic mechanisms of chronic pain and offers clinicians new therapeutic perspectives targeting the above mechanisms in both painful disorders. (C) 2007 by the American Pain Society.

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