Comparison of GFAP and UCH-L1 Measurements Using Two Automated Immunoassays (i-STAT ® and Alinity ® ) for the Management of Patients with Mild Traumatic Brain Injury: Preliminary Results from a French Single-Center Approach.
Charlotte OrisClara Khatib-ChahidiBruno PereiraValentin Bailly DefranceDamien BouvierVincent SapinPublished in: International journal of molecular sciences (2024)
The measurement of blood glial fibrillary acidic protein (GFAP) and ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) may assist in the management of mild traumatic brain injury (mTBI). This study aims to compare GFAP and UCH-L1 values measured using a handheld device with those measured using a core laboratory platform. We enrolled 230 mTBI patients at intermediate risk of complications. Following French guidelines, a negative S100B value permits the patient to be discharged without a computed tomography scan. Plasma GFAP and UCH-L1 levels were retrospectively measured using i-STAT ® and Alinity ® i analyzers in patients managed within 12 h post-trauma. Our analysis indicates a strong correlation of biomarker measurements between the two analyzers. Cohen's kappa coefficients and Lin's concordance coefficients were both ≥0.7, while Spearman's correlation coefficient was 0.94 for GFAP and 0.90 for UCH-L1. Additionally, the diagnostic performance in identifying an intracranial lesion was not significantly different between the two analyzers, with a sensitivity of 100% and specificity of approximately 30%. GFAP and UCH-L1 levels measured using Abbott's i-STAT ® and Alinity ® i platform assays are highly correlated both analytically and clinically in a cohort of 230 patients managed for mTBI according to French guidelines.
Keyphrases
- mild traumatic brain injury
- computed tomography
- end stage renal disease
- newly diagnosed
- high throughput
- ejection fraction
- prognostic factors
- cell proliferation
- peritoneal dialysis
- magnetic resonance imaging
- immune response
- risk factors
- clinical practice
- magnetic resonance
- case report
- inflammatory response
- nuclear factor
- binding protein
- ionic liquid
- patient reported