4.5 Article

Biokinetic Analysis of Ubiquitin C-Terminal Hydrolase-L1 (UCH-L1) in Severe Traumatic Brain Injury Patient Biofluids

期刊

JOURNAL OF NEUROTRAUMA
卷 28, 期 6, 页码 861-870

出版社

MARY ANN LIEBERT INC
DOI: 10.1089/neu.2010.1564

关键词

biomarkers; clinical trial; neural injury; outcome measures; traumatic brain injury

资金

  1. Department of Defense [DoD W81XWH-06-1-0517]
  2. National Institutes of Health [R01 NS052831]

向作者/读者索取更多资源

Ubiquitin C-terminal hydrolase-L1 (UCH-L1) is a neuron-specific enzyme that has been identified as a potential biomarker of traumatic brain injury (TBI). The study objectives were to determine UCH-L1 exposure and kinetic metrics, determine correlations between biofluids, and assess outcome correlations in severe TBI patients. Data were analyzed from a prospective, multicenter study of severe TBI (Glasgow Coma Scale [GCS] score <= 8). Cerebrospinal fluid (CSF) and serum data from samples taken every 6 h after injury were analyzed by enzyme-linked immunosorbent assay (ELISA). UCH-L1 CSF and serum data from 59 patients were used to determine biofluid correlations. Serum samples from 86 patients and CSF from 59 patients were used to determine outcome correlations. Exposure and kinetic metrics were evaluated acutely and up to 7 days post-injury and compared to mortality at 3 months. There were significant correlations between UCH-L1 CSF and serum median concentrations (r(s) = 0.59, p < 0.001), AUC (r(s) = 0.3, p = 0.027), Tmax (r(s) = 0.68, p < 0.001), and MRT (r(s) = 0.65, p < 0.001). Outcome analysis showed significant increases in median serum AUC (2016 versus 265 ng/mL(star)min, p = 0.006), and Cmax (2 versus 0.4 ng/mL, p = 0.003), and a shorter Tmax (8 versus 19 h, p = 0.04) in those who died versus those who survived, respectively. In the first 24 h after injury, there was a statistically significant acute increase in CSF and serum median Cmax((0-24h)) in those who died. This study shows a significant correlation between UCH-L1 CSF and serum median concentrations and biokinetics in severe TBI patients, and relationships with clinical outcome were detected.

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