• Frederick K Korley, Ramon Diaz-Arrastia, Alan H B Wu, John K Yue, Geoffrey T Manley, Haris I Sair, Jennifer Van Eyk, Allen D Everett, TRACK-TBI investigators, David O Okonkwo, Alex B Valadka, Wayne A Gordon, Andrew I R Maas, Pratik Mukherjee, Esther L Yuh, Hester F Lingsma, Ava M Puccio, and David M Schnyer.
• 1 Department of Emergency Medicine, Johns Hopkins University School of Medicine , Baltimore, Maryland.
• J. Neurotrauma. 2016 Jan 15; 33 (2): 215-25.

AbstractBrain-derived neurotrophic factor (BDNF) is important for neuronal survival and regeneration. We investigated the diagnostic and prognostic values of serum BDNF in traumatic brain injury (TBI). We examined serum BDNF in two independent cohorts of TBI cases presenting to the emergency departments (EDs) of the Johns Hopkins Hospital (JHH; n = 76) and San Francisco General Hospital (SFGH, n = 80), and a control group of JHH ED patients without TBI (n = 150). Findings were subsequently validated in the prospective, multi-center Transforming Research and Clinical Knowledge in TBI (TRACK-TBI) Pilot study (n = 159). We investigated the association between BDNF, glial fibrillary acidic protein (GFAP), and ubiquitin C-terminal hydrolase-L1 (UCH-L1) and recovery from TBI at 6 months in the TRACK-TBI Pilot cohort. Incomplete recovery was defined as having either post-concussive syndrome or a Glasgow Outcome Scale Extended score <8 at 6 months. Median day-of-injury BDNF concentrations (ng/mL) were lower among TBI cases (JHH TBI, 17.5 and SFGH TBI, 13.8) than in JHH controls (60.3; p = 0.0001). Among TRACK-TBI Pilot subjects, median BDNF concentrations (ng/mL) were higher in mild (8.3) than in moderate (4.3) or severe TBI (4.0; p = 0.004. In the TRACK-TBI cohort, the 75 (71.4%) subjects with very low BDNF values (i.e.,

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