Measurement of S100B protein: evaluation of a new prototype on a bioMérieux Vidas® 3 analyzer
-
Charlotte Oris
, Russel Chabanne , Julie Durif , Samy Kahouadji , Marina Brailova , Vincent Sapin and Damien Bouvier
Abstract
Background
The addition of S100B protein to guidelines for the management of mild traumatic brain injury (mTBI) decreases the amount of unnecessary computed tomography (CT) scans with a significant decrease in radiation exposure and an increase in cost savings. Both DiaSorin and Roche Diagnostics have developed automated assays for S100B determination. Recently, bioMérieux developed a prototype immunoassay for serum S100B determination. For the first time, we present the evaluation of the S100B measurement using a bioMérieux Vidas® 3 analyzer.
Methods
We evaluated the matrix effects of serum and plasma, and their stability after storage at 2–8 °C, −20 °C and −80 °C. The new measurement prototype (bioMérieux) was compared with an established one (Roche Diagnostics), and a precision study was also conducted. Lastly, clinical diagnostics performance of the bioMérieux and Roche Diagnostics methods were compared for 80 patients referred to the Emergency Department for mTBI.
Results
Stability after storage at 2–8 °C, −20 °C, and −80 °C and validation of the serum matrix were demonstrated. The bioMérieux analyzer was compared to the Roche Diagnostics system, and the analytical precision was found to be efficient. Clinical diagnosis performance evaluation confirmed the predictive negative value of S100B in the management of mTBI.
Conclusions
The study’s data are useful for interpreting serum S100B results on a bioMérieux Vidas® 3 analyzer.
Acknowledgments
We thank the Emergency Department and the Neurological Intensive Care Unit at Clermont-Ferrand Hospital for their help in specimen collection. We wish to acknowledge the excellent technical assistance of Laure Allard, Frédérique Raymond and Corinne Perret.
Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: This work was supported by the bioMérieux company.
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.
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©2019 Walter de Gruyter GmbH, Berlin/Boston
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Articles in the same Issue
- Frontmatter
- Editorials
- CCLM Award for the Most Cited Paper
- Folate and vitamin B12 assays after recalibration to the WHO International Standard 03/178: making the interpretation as simple as possible, but not simpler
- Reviews
- Blood contamination in salivary diagnostics: current methods and their limitations
- Central adrenal insufficiency: open issues regarding diagnosis and glucocorticoid treatment
- Genetics and Molecular Diagnostics
- Measuring the chronology of the translational process of molecular genetic discoveries
- Development and interlaboratory evaluation of a NIST Reference Material RM 8366 for EGFR and MET gene copy number measurements
- General Clinical Chemistry and Laboratory Medicine
- Post-translational modification-derived products are associated with frailty status in elderly subjects
- Urine chloride self-measurement to monitor sodium chloride intake in patients with chronic kidney disease
- Estimated urinary osmolality based on combined urinalysis parameters: a critical evaluation
- Measurement of S100B protein: evaluation of a new prototype on a bioMérieux Vidas® 3 analyzer
- Measuring thyroglobulin in patients with thyroglobulin autoantibodies: evaluation of the clinical impact of BRAHMS Kryptor® Tg-minirecovery test in a large series of patients with differentiated thyroid carcinoma
- Human chorionic gonadotropin suspected heterophile interference investigations in immunoassays: a recommended approach
- Certified reference material against PR3 ANCA IgG autoantibodies. From development to certification
- Diagnostic accuracy of a fully automated multiplex celiac disease antibody panel for serum and plasma
- Fasting serum bile acids concentration is associated with insulin resistance independently of diabetes status
- Hematology and Coagulation
- The association between activated protein C ratio and Factor V Leiden are gender-dependent
- Reference Values and Biological Variations
- Determination of sigma score based on biological variation for haemostasis assays: fit-for-purpose for daily practice?
- Calcitonin measurement in pediatrics: reference ranges are gender-dependent, validation in medullary thyroid cancer and thyroid diseases
- Cancer Diagnostics
- Uncovering the clinical impact of kallikrein-related peptidase 5 (KLK5) mRNA expression in the colorectal adenoma-carcinoma sequence
- Cardiovascular Diseases
- Performance of a novel high sensitivity cardiac troponin I assay in asymptomatic hemodialysis patients – evidence for sex-specific differences
- Infectious Diseases
- Rapid susceptibility testing of multi-drug resistant Escherichia coli and Klebsiella by glucose metabolization monitoring
- Letters to the Editor
- Vitamin B12 and folate levels in a healthy population: establishing reference intervals
- Reference values of a new serum folate assay traceable to the WHO International Standard
- Serum protein electrophoresis and complement deficiencies: a veteran but very versatile test in clinical laboratories
- Introduction of a novel ELISA assay for serum AMH determination
- Bone alkaline phosphatase on the IDS-iSYS automated analyser; cross-reactivity with intestinal ALP
- Evaluation of the MULTISURE HIV Rapid Test in a Korean population with low human immunodeficiency virus prevalence
- Vancomycin immunoassay: does the Advia Centaur XPT underestimate the exposure of patients? A method comparison study
- Hb Hunan and Hb Hengyang: Two unexpected discoveries during HbA1c measurements
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- Implementation of an automated method for direct quantification of urinary ammonium
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