Serum GFAP - pediatric reference interval in a cohort of Danish children

Lea Tybirk1, Claus Vinter Bødker Hviid1,2,3,4, Cindy Soendersoe Knudsen1

  • 1Department of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark.

Insights

This study establishes a reference interval for glial fibrillary acidic protein (GFAP) in children's blood. These findings are crucial for diagnosing brain injuries and neurological diseases in pediatric patients.

Area of Science:

  • Biomarkers
  • Pediatric Neurology
  • Clinical Chemistry

Background:

  • Glial fibrillary acidic protein (GFAP) is a key biomarker for brain injury and neurological conditions.
  • Establishing a reliable reference interval (RI) for serum GFAP in children is essential for its clinical application.
  • Current clinical use of GFAP in pediatric populations is hindered by the absence of age-specific RIs.

Purpose of the Study:

  • To develop an age-dependent, continuous reference interval (RI) for serum glial fibrillary acidic protein (GFAP) in children.
  • To provide a foundational dataset for the clinical interpretation of GFAP levels in pediatric patients.
  • To address the limitations in using GFAP as a biomarker in children due to the lack of established RIs.

Main Methods:

  • Serum samples from 391 children aged 0.4 to 17.9 years were analyzed using a single-molecule array (Simoa) assay.
  • Non-parametric quantile regression was employed to model a continuous reference interval.
  • The continuous RI was visualized graphically and presented in a tabulated format with discrete one-year intervals.

Main Results:

  • Serum GFAP levels exhibited a significant age-dependent pattern, decreasing with age from infancy to adolescence.
  • Median GFAP levels decreased by 66% between four months and five years of age, and by another 65% between five and 17.9 years of age.
  • No statistically significant differences in serum GFAP levels were observed between genders.

Conclusions:

  • This research successfully established an age-dependent reference interval for serum GFAP in children.
  • The findings highlight elevated GFAP levels and greater variability during the early years of life.
  • The developed RI will aid clinicians in the accurate interpretation of GFAP as a biomarker in pediatric neurological assessments.
Abstract