Characterisation of serum total tau following paediatric traumatic brain injury: a case-control study
| Autor: | Alison Crichton, Amy A. Wilkinson, Helena Frndova, Anne-Marie Guerguerian, Carmel Delzoppo, Catherine Farrell, Kathy Boutis, Cheryl L. Wellington, Miriam H. Beauchamp, Jasmine Gill, Khosrow Adeli, Serum Biomarkers, Sophie Stukas, Franz E Babl, Vicki Anderson, Jamie Hutchison, Victoria Higgins, Evyatar Hubara, Mardee Greenham |
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| Rok vydání: | 2019 |
| Předmět: |
Male
medicine.medical_specialty Adolescent Birth trauma Traumatic brain injury tau Proteins law.invention 03 medical and health sciences Young Adult 0302 clinical medicine law Reference Values 030225 pediatrics Internal medicine Brain Injuries Traumatic Developmental and Educational Psychology Medicine Humans 030212 general & internal medicine Young adult Child business.industry Glasgow Coma Scale Age Factors Infant Emergency department Venous blood medicine.disease Intensive care unit 3. Good health Case-Control Studies Child Preschool Pediatrics Perinatology and Child Health Cohort Female business Tomography X-Ray Computed Biomarkers |
| Zdroj: | The Lancet. Childadolescent health. 3(8) |
| ISSN: | 2352-4650 |
| Popis: | Summary Background Traumatic brain injury (TBI) is a major health problem in children. Blood-based biomarkers interpreted by use of normative values might improve the accuracy of diagnosis. Ultrasensitive assays can quantify serum concentrations of the neuronal microtubule-associated protein tau, which is increased in adult brains following TBI. We aimed to determine if serum total tau correlates with TBI diagnosis, severity, and radiological findings on CT scans in children younger than 18 years. Methods In this case-control study, we included venous blood samples from healthy control children in the Canadian Laboratory Initiative on Pediatric Reference Intervals (CALIPER) biobank. For TBI cases, we recruited children (aged 0–17 years) who presented to the emergency department within 24 h of a TBI in three tertiary-care paediatric hospitals (Toronto, Vancouver, and Melbourne). Children were eligible if they required hospital observation for a minimum of 4 h or admission to the intensive care unit, and were excluded if they had had hospital treatment for a previous TBI, had birth trauma, or their parents could not speak English or French and therefore could not readily give consent. All available control samples were used and a case-control match was therefore not done. Venous and arterial blood samples were collected from patients with TBI within 28 h of injury (day 1). We used an ultrasensitive single-molecule immunoassay to measure serum total tau in blood samples. We first generated reference intervals of serum total tau from the control group, and used these normative data to interpret injury-associated changes in serum total tau in children with TBI. Concentrations of serum tau were measured in all CALIPER participants and patients with TBI, and no participants were excluded before analysis. Findings We included samples from 416 control participants from the CALIPER cohort. Median total tau concentrations did not differ between sexes (p=0·12), but three significant reference intervals based on age groups were identified (1–3 years [0·88–19·2 pg/mL], 4–15 years [0·93–5·31 pg/mL], and 16–19 years [0·79–4·20 pg/mL]). Blood samples were obtained from 158 patients with TBI recruited between April 30, 2011, and June 28, 2013. Serum total tau on day 1 of TBI was negatively associated with Glasgow Coma Scale (GCS) score (rs=–0·42, 95% CI −0·55 to −0·28, p Interpretation Serum total tau might help to differentiate between patients with mild TBI (GCS 13–14 vs GCS 15), but larger studies are needed to validate these results before this biomarker can be used for diagnosis and prognosis. Funding Canadian Institutes of Health Research, Ontario Neurotrauma Foundation, and Victoria Neurotrauma Foundation |
| Databáze: | OpenAIRE |
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