Plasma brain-derived neurotrophic factor levels after severe traumatic brain injury

Brain Inj. 2016;30(1):23-8. doi: 10.3109/02699052.2015.1077993. Epub 2015 Nov 10.

Abstract

Objective: Severe traumatic brain injury (TBI) is associated with a 30-70% mortality rate. Nevertheless, in clinical practice there are no effective biomarkers for the prediction of fatal outcome following severe TBI. Therefore, the aim was to determine whether brain-derived neurotrophic factor (BDNF) plasma levels are associated with intensive care unit (ICU) mortality in patients with severe TBI.

Methods: This prospective study enrolled 120 male patients who suffered severe TBI (Glasgow Coma Scale 3-8 at emergency room admission). The plasma BDNF level was determined at ICU admission (mean 6.4 hours after emergency room admission).

Results: Severe TBI was associated with a 35% mortality rate and 64% of the patients presented severe TBI with multi-trauma. The mean plasma BDNF concentration among the severe TBI victims was 704.2 ± 63.4 pg ml(-1) (±SEM). Nevertheless, there were no significant differences between BDNF levels in the survivor (700.2 ± 82.8 pg ml(-1)) or non-survivor (711.6 ± 97.4 pg ml(-1)) groups (p = 0.238) or in the isolated TBI (800.4 ± 117.4 pg ml(-1)) or TBI with multi-trauma groups (650.5 ± 73.9 pg ml(-1)) (p = 0.109).

Conclusions: Plasma BDNF concentrations did not correlate with either short-term fatal outcome or type of injury following severe TBI.

Keywords: BDNF; biomarker; multi-trauma; outcome; severe TBI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Biomarkers / blood
  • Brain Injuries, Traumatic / blood*
  • Brain-Derived Neurotrophic Factor / blood*
  • Glasgow Coma Scale
  • Humans
  • Male
  • Middle Aged
  • Prospective Studies
  • ROC Curve
  • Treatment Outcome

Substances

  • Biomarkers
  • Brain-Derived Neurotrophic Factor
  • BDNF protein, human