• Title of article

    Effect of Sample Processing Delays on the Values of Serum Based Biomarkers of Brain Injury Collected from the Umbilical Cord Blood of Neonates

  • Author/Authors

    Weiss, Michael D Department of Pediatrics - Division of Neonatology - University of Florida, United States of America , Bliznyuk, Nikolay A Department of Agricultural and Biological Engineering - University of Florida, United States of America , Rossignol, Candace C Department of Pediatrics - Division of Neonatology - University of Florida, United States of America , Sura, Livia Department of Pediatrics - Division of Neonatology - University of Florida, United States of America , Huene, Melissa Department of Pediatrics - Division of Neonatology - University of Florida, United States of America , Copenhaver, Nicole Department of Pediatrics - Division of Neonatology - University of Florida, United States of America , Glushakova, Olena Department of Neurosurgery - Virgina Commonwealth University, United States of America , Hayes, Ronald L Department of Clinical and Health Psychology - University of Florida, United States of America

  • Pages
    7
  • From page
    10
  • To page
    16
  • Abstract
    Background: When a neonate is born with suspected brain injury, blood samples are often obtained from the umbilical cord blood but are not always processed immediately. Objective: Test the accuracy of brain injury biomarker assays on samples that experienced delayed processing. Methods: Healthy neonates who did not have risk factors for brain injury provided cord blood samples. Group 1 blood samples were centrifuged immediately, and the serum was removed and frozen at baseline, 4, and 8 hours. Group 2 had a baseline sample processed immediately and then blood samples remained in contact with the clotted portion until 4, and 8 hours and then were centrifuged. Enzyme-linked immunosorbent assays determined the concentrations of Ubiquitin C-Terminal Hydrolase L1 (UCH-L1) and Glial Fibrillary Acidic Protein (GFAP). Results: Group 1’s average concentrations of GFAP were 62±47 pg/ml at 0 hours (n=32) with a mean increase of 3±14% and a decrease of 0.2±9% at 4 and 8 hours, respectively. UCH-L1 average concentrations were 3306±3093 pg/ml at 0 hours (n=37) with a mean increase of 3±10% at 4 hours and a mean decrease of 0.6±11% at 8 hours. Group 2’s average GFAP concentrations were 104±111 pg/ml at 0 hours (n=9) with a mean decrease of 5±9% and 7±7% at 4 and 8 hours, respectively. UCH-L1 average concentrations were 3448±2456 pg/ml at 0 hour (n=8) with a mean increase of 9±6% and 6±18% at 4 and 8 hours, respectively. Conclusion: Delays in processing up to 8 hours did not significantly affect the concentration of UCH-L1 or GFAP.
  • Keywords
    Hypoxic-ischemic Encephalopathy , Biomarkers , Neonates , GFAP , UCH-L1 , Brain injury
  • Journal title
    Open Biomarkers Journal
  • Serial Year
    2019
  • Record number

    2559009