We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
Sekisui Diagnostics

Download Mobile App




Blood Test Detects Traumatic Brain Injury Reducing Unnecessary Imaging

By LabMedica International staff writers
Posted on 02 Jun 2015
A simple blood test to measure brain-specific proteins released after a person suffers a traumatic brain injury (TBI) can reliably predict both evidence of TBI on radiographic imaging and injury severity.

There is a potential benefit of adding detection of glial fibrillary acidic protein breakdown products (GFAP-BDP) to clinical screening with computed tomography (CT) and magnetic resonance imaging (MRI).

An international team of scientists led by those at University of Pittsburgh Medical Center (PA, USA) analyzed blood levels of GFAP-BDP from patients ages 16 to 93 years treated at multiple trauma centers for suspected TBI. More...
They evaluated the ability of the blood-based biomarker to predict intracranial injury as compared to the findings on an admission CT and a delayed MRI scan. A total of 215 patients were available for analysis and approximately 73% of patients were male.

Serum samples were collected within 24 hours of injury and were dated and time stamped to compare with time of injury. Blinded sample analysis was performed in a single laboratory (Banyan Biomarkers; Alachua, FL, USA) using a sandwich enzyme-linked immunosorbent assay (ELISA) to GFAP-BDP. The GFAP ELISA utilized a proprietary mouse monoclonal antibody for solid-phase immobilization, and a proprietary polyclonal rabbit antibody for detection.

GFAP-BDP level was the most accurate predictor of the presence or absence of intracranial injury detected by radiographic imaging (accuracy, 81%), as compared with accepted clinical predictors of intracranial injury.

The authors reported a net benefit for the use of GFAP-BDP above imaging-based screening alone and a net reduction in unnecessary scans by 12% to 30%. Calculation of a cut-off value to maximize accuracy in the mild and moderate injury range specifically yielded a GFAP-BDP level of 0.6 ng/mL, with a sensitivity of 67%, a specificity of 89%, and a Brier score of 0.21. A cut-off value to maximize specificity was calculated at a GFAP-BDP concentration of 1.66 ng/mL, resulting in a sensitivity of 45%, specificity of 99%, and a Brier score of 0.29.

John T. Povlishock, PhD, a professor at Virginia Commonwealth University (Richmond, VA, USA) said, “Importantly, this study significantly expands upon other studies that speak to the usefulness of GFAP and, specifically, serum-derived GFAP-BDP in identifying those traumatically brain injured patients whose clinical course is complicated by intracranial injury, demonstrating that GFAP-BDP offers good predictive ability, significant discrimination of injury severity, and net benefit in reducing the need for unnecessary scans, all of which have significant implications for the brain-injured patient.” The study was published on April 7, 2015, in the Journal of Neurotrauma.

Related Links:

University of Pittsburgh Medical Center 
Banyan Biomarkers 
Virginia Commonwealth University 



Platinum Member
Automated Coagulation Analyzer
Hemolumi H6
βeta-Hydroxybutyrate Reagent
β-Hydroxybutyrate LiquiColor®
New
Slide Scanner System
NanoZoomer S540MD
Gold Member
Platelet Function Analyzer
PL-12
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Immunology

view channel
Image Credit: iStock

Antibody Profiling Predicts Inflammatory Bowel Disease Years Before Diagnosis

Inflammatory bowel disease (IBD), which includes Crohn’s disease and ulcerative colitis, involves abnormal immune responses that cause persistent inflammation and damage in the digestive system.... Read more

Pathology

view channel
Image Credit: iStock

AI Tissue Analysis May Help Identify Missed Precancerous Colon Polyps

Colorectal cancer is diagnosed in an estimated 1.9 million people worldwide each year, often without symptoms in its early stages. Timely detection of precancerous lesions is therefore important, yet some... Read more

Technology

view channel
Image: Signals LabGistics uses AI to turn natural-language instructions and SOPs into coordinated scientific workflows, helping connect teams, systems, and processes. (Photo courtesy of Revvity)

New AI-Powered System Aims to Streamline Laboratory and Manufacturing Workflows

Scientific laboratories supporting drug development, biotechnology, and materials research increasingly rely on coordinated digital workflows to move data, samples, and activities across teams.... Read more

Industry

view channel
Image: Beginning in 2027, Quest will provide access to the Onclarity Self-Collection Kit through clinician, health plan, and consumer-initiated testing channels, along with its patient service center network.

Collaboration to Expand Cervical Cancer Screening Access With At-Home HPV Collection

Cervical cancer is largely preventable with regular screening and early detection of human papillomavirus (HPV), the leading cause of the disease. Screening gaps persist, in part because traditional sample... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.