Traumatic brain injury (TBI) is a substantial health care issue affecting both civilian and military populations. Although extremes of head injury are recognizable, mild to moderate TBI (MMTBI) is more difficult to diagnose leading to a need for the identification of circulating biomarkers of brain injury that may facilitate early identification. Using a rat model of TBI we identified a novel marker of neuronal injury, visinin like protein 1 (VILIP-1), that is released into blood rapidly after injury. To facilitate rapid measurement of circulating VILIP-1 we developed a combined lateral flow device (LFD) that provides detection of the biomarker in less than 20 min. Although initial testing in human TBI patients are promising there is a need for further testing in blood samples drawn clinically well characterized TBI patients soon after injury.
The aim of the current proposal is to further validate the use of our LFD as a point of care diagnostic for TBI using a combination of archived serum samples from normal control subjects as well as patients with systemic traumatic injuries but no TBI and subjects with mild to moderate TBI and whole blood samples from patients being evaluated in the emergency department of Orlando Regional Medical Center. If successful, the proposed studies will validate the use of our VILIP-1 LFD for rapid in field detection of MMTBI and will provide the preliminary data to support a larger clinical trial of the device that could ultimately benefit both civilian and military populations.

Public Health Relevance

Traumatic brain injury (TBI) is a substantial health care issue affecting both civilian and military populations. Despite considerable research there remains a critical need for a biomarker test that can rapidly measure a maker of mild to moderate TBI (MMTBI) in blood or cerebrospinal fluid and provide identification of patient during a clinically useful time frame. Preliminary and future studies described in this proposal aim to test the usefulness of a lateral flow device (LFD) that quantifies visinin like protein 1 (VILIP-1), a neuron specific Ca2+-sensor protein released into blood following TBI.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21NS099781-02
Application #
9355051
Study Section
Acute Neural Injury and Epilepsy Study Section (ANIE)
Program Officer
Bellgowan, Patrick S F
Project Start
2016-09-30
Project End
2019-08-31
Budget Start
2017-09-01
Budget End
2019-08-31
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Kentucky
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
939017877
City
Lexington
State
KY
Country
United States
Zip Code
40526