Literature DB >> 24362070

BDNF serum levels in subjects developing or not post-traumatic stress disorder after trauma exposure.

Francesco Angelucci1, Valerio Ricci2, Francesca Gelfo2, Giovanni Martinotti3, Marcella Brunetti3, Gianna Sepede3, Maria Signorelli4, Eugenio Aguglia4, Mauro Pettorruso5, Federica Vellante3, Massimo Di Giannantonio3, Carlo Caltagirone2.   

Abstract

Post-traumatic stress disorder (PTSD) is a syndrome resulting from exposure to a severe traumatic event that poses threatened death or injury and produces intense fear and helplessness. The neural structures implicated in PTSD development belong to the limbic system, an important region for emotional processing. Brain-derived neurotrophic factor (BDNF) is a neurotrophin that serves as survival factor for selected populations of central nervous system (CNS) neurons and plays a role in the limbic system by regulating synaptic plasticity, memory processes and behavior. Impaired BDNF production in the brain can lead to a variety of CNS dysfunctions including symptoms associated with PTSD. However, so far fewer studies have investigated this neurotrophin in patients with PTSD. Furthermore, given the multiple role of BDNF in various CNS disorders, it cannot be excluded that traumatic events per se may influence neurotrophin levels, without a direct association to the PTSD syndrome. To elucidate these issues, in this study we analyzed BDNF serum levels in two groups of subjects: patients with trauma exposure who developed PTSD, and subjects with trauma exposure who did not develop PTSD. We found that BDNF serum levels were lower in PTSD patients as compared to related control subjects. Thus, these data suggest that BDNF might be involved in pathophysiology of PTSD and consequently therapeutic approaches aimed at restoring BDNF serum levels may be beneficial to this pathology.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  BDNF; ELISA; Post-traumatic stress disorder; Trauma exposure

Mesh:

Substances:

Year:  2013        PMID: 24362070     DOI: 10.1016/j.bandc.2013.11.012

Source DB:  PubMed          Journal:  Brain Cogn        ISSN: 0278-2626            Impact factor:   2.310


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