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Updated: May 14, 2026

Systems Analysis of the Neuroinflammatory and Hemodynamic Response to Traumatic Brain Injury
Published on: May 27, 2022
Plasma copeptin concentration and outcome after pediatric traumatic brain injury
Chao Lin1, Ning Wang, Zhi-Peng Shen
1Department of Neurosurgery, The Children's Hospital, Zhejiang University, School of Medicine, Hangzhou 310003, China.
Insights
Elevated plasma copeptin levels in children with traumatic brain injury (TBI) predict poor outcomes. This biomarker shows potential for predicting mortality and unfavorable outcomes following TBI.
Area of Science:
- Biomarkers in pediatric critical care
- Neurology and neurosurgery
- Clinical diagnostics
Background:
- Higher plasma copeptin levels are linked to adverse outcomes in critical illness.
- Traumatic brain injury (TBI) in children can lead to severe consequences.
Purpose of the Study:
- To measure plasma copeptin concentrations in children with acute severe TBI.
- To analyze the correlation between copeptin levels and disease outcomes at 6 months post-injury.
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) was used to measure plasma copeptin.
- Plasma copeptin levels were compared between 126 children with TBI and 126 healthy children.
- Statistical analysis included odds ratios, confidence intervals, and area under the curve (AUC) for predictive value.
Main Results:
- Children with TBI had significantly higher plasma copeptin levels than healthy children (46.2±20.8 pmol/L vs. 9.6±3.0 pmol/L, P<0.001).
- Plasma copeptin was an independent predictor of 6-month mortality (OR 1.261) and unfavorable outcome (OR 1.313).
- Copeptin improved the predictive accuracy for unfavorable outcomes when combined with the Glasgow Coma Scale (GCS) score.
Conclusions:
- Plasma copeptin is a novel and valuable biomarker for predicting 6-month clinical outcomes in pediatric TBI.
- Copeptin levels offer significant predictive value for mortality and functional recovery in children with TBI.
- Further research can explore the clinical utility of copeptin in TBI management.
Abstract:
Higher plasma copeptin level has been associated with poor outcomes of critical illness. The present study was undertaken to investigate the plasma copeptin concentrations in children with traumatic brain injury (TBI) and to analyze the correlation of copeptin with disease outcome. Plasma copeptin concentrations of 126 healthy children and 126 children with acute severe TBI were measured by enzyme-linked immunosorbent assay. Twenty-one patients (16.7%) died and 38 patients (30.2%) had an unfavorable outcome (Glasgow Outcome Scale score of 1-3) at 6 months. Plasma copeptin level was obviously higher in patients than in healthy children (46.2±20.8 pmol/L vs. 9.6±3.0 pmol/L, P<0.001). Plasma copeptin level was identified as an independent predictor for 6-month mortality [odds ratio (OR) 1.261, 95% confidence interval (CI) 1.112-1.538, P=0.005] and unfavorable outcome (OR 1.313, 95% CI 1.146-1.659, P=0.003). The predictive value of copeptin was similar to that of Glasgow Coma Scale (GCS) score for 6-month mortality [area under curve (AUC) 0.832, 95% CI 0.755-0.892 vs. AUC 0.873, 95% CI 0.802-0.926, P=0.412] and unfavorable outcome (AUC 0.863, 95% CI 0.790-0.918 vs. AUC 0.885, 95% CI 0.816-0.935, P=0.596). Copeptin improved the AUC of GCS score for 6-month unfavorable outcome (AUC 0.929, 95% CI 0.869-0.967, P=0.013), but not for 6-month mortality (AUC 0.887, 95% CI 0.818-0.936, P=0.600). Thus, plasma copeptin level represents a novel biomarker for predicting 6-month clinical outcome in children with TBI.
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