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Abstract Details

Measurement of inflammatory cytokines and neurodegenerative/injury biomarkers in acute concussion/mild traumatic brain injury (c/mTBI) serum and saliva samples
Neuro Trauma, Critical Care, and Sports Neurology
P11 - Poster Session 11 (8:00 AM-9:00 AM)
5-009

Early time point (<24 hrs) levels of serum and saliva t-Tau, NF-L, GFAP, UCH-L1 and IL-6, IL-10, TNF-α, were measured to evaluate identification of acute c/mTBI patients versus healthy controls.

Elevations in certain central nervous system (CNS) proteins (t-Tau, NF-L, GFAP and UCH-L1) and inflammatory cytokines (IL-6, IL-10, TNFα) in blood and CSF samples have been associated with c/mTBI. Recent studies showed the combination of neurodegenerative proteins and inflammatory cytokines provided excellent prognostic information with regards to 6 month full recovery, suggesting evaluation for identification of acute injury. 

The SIMOA Neurology 4-plex A and Cytokine 3-plex A immunoassays (Quanterix) were used to measure t-Tau, NF-L, GFAP, UCH-L1 and IL-6, IL-10, TNFα in serum and saliva respectively from acute c/mTBI samples versus controls.  Blood samples were collected from study subjects (n= 30 each) within 1-4 hr and 8-16 hr post-c/mTBI injury, as well as 30 healthy controls. Matching saliva samples were also collected from the 8-16 hr post-c/mTBI subgroup (n= 30).

IL-6, IL-10 and TNFα were significantly elevated in the 1-4 hr and 8-16 hr post-c/mTBI serum samples relative to healthy controls (p <0.0001). Receiving Operating Characteristic (ROC) curve analysis indicates that each of the 3 cytokines is discriminatory for c/mTBI patients vs healthy controls (AUC = 0.86-0.99). Median levels of GFAP, NF-L, UCH-L1 and t-Tau were significantly elevated in 1-4 hr and 8-16 hr post-c/mTBI serum samples relative to healthy controls. ROC analysis of neuronal biomarkers indicate moderate discriminatory ability for c/mTBI vs controls (AUC = 0.7-0.76). With the exception of IL-6, all the biomarkers levels in most saliva samples were very low.

The measurement of CNS proteins and inflammatory cytokines as biomarkers of c/mTBI may enhance diagnostic capability as well as prognosis with regards to the severity and outcome of brain injuries.

Authors/Disclosures
Ahmed Chenna, PhD (Monogram Biosciences Inc)
PRESENTER
Dr. Chenna has received personal compensation for serving as an employee of LabCorp-monogram Biosciences. Dr. Chenna has or had stock in LabCorp.
John Winslow, PhD (Monogram Biosciences Inc., Laboratory Corporation of America) Dr. Winslow has received personal compensation for serving as an employee of Labcorp/Monogram Biosciences. Dr. Winslow has received personal compensation for serving as an employee of Labcorp/Monogram Biosciences. Dr. Winslow has stock in Labcorp. Dr. Winslow has received intellectual property interests from a discovery or technology relating to health care.
Christos J. Petropoulos, PhD (Monogram Biosciences, LabCorp) Dr. Petropoulos has received personal compensation for serving as an employee of Labcorp-Monogram Biosciences. Dr. Petropoulos has stock in Laboratory Corporation of America Holdings. Dr. Petropoulos has received intellectual property interests from a discovery or technology relating to health care.