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Blood biomarkers on admission in acute traumatic brain injury: Relations to severity, CT findings and care path in the CENTER-TBI study

Vyvere TV; Richter S; Steyerberg EW; Gravesteijn BY; Büki A; CENTER-TBI Participants and Investigators; Wang KKW; Yang Z; Menon DK; Lecky F; Xu H; Maas AIR; Czeiter E; Mondello S; Newcombe VFJ; Amrein K; Verheyden J

Blood biomarkers on admission in acute traumatic brain injury: Relations to severity, CT findings and care path in the CENTER-TBI study

Vyvere TV
Richter S
Steyerberg EW
Gravesteijn BY
Büki A; CENTER-TBI Participants and Investigators
Wang KKW
Yang Z
Menon DK
Lecky F
Xu H
Maas AIR
Czeiter E
Mondello S
Newcombe VFJ
Amrein K
Verheyden J
Katso/Avaa
Publishers's PDF (3.696Mb)
Lataukset: 

Elsevier
doi:10.1016/j.ebiom.2020.102785
URI
https://www.sciencedirect.com/science/article/pii/S2352396420301602?via=ihub
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2021042823513
Tiivistelmä

Background

Serum biomarkers may inform and improve care in traumatic brain injury (TBI). We aimed to correlate serum biomarkers with clinical severity, care path and imaging abnormalities in TBI, and explore their incremental value over clinical characteristics in predicting computed tomographic (CT) abnormalities.

Methods

We analyzed six serum biomarkers (S100B, NSE, GFAP, UCH-L1, NFL and t-tau) obtained <24 h post-injury from 2867 patients with any severity of TBI in the Collaborative European NeuroTrauma Effectiveness Research (CENTER-TBI) Core Study, a prospective, multicenter, cohort study. Univariable and multivariable logistic regression analyses were performed. Discrimination was assessed by the area under the receiver operating characteristic curve (AUC) with 95% confidence intervals.

Findings

All biomarkers scaled with clinical severity and care path (ER only, ward admission, or ICU), and with presence of CT abnormalities. GFAP achieved the highest discrimination for predicting CT abnormalities (AUC 0•89 [95%CI: 0•87–0•90]), with a 99% likelihood of better discriminating CT-positive patients than clinical characteristics used in contemporary decision rules. In patients with mild TBI, GFAP also showed incremental diagnostic value: discrimination increased from 0•84 [95%CI: 0•83–0•86] to 0•89 [95%CI: 0•87–0•90] when GFAP was included. Results were consistent across strata, and injury severity. Combinations of biomarkers did not improve discrimination compared to GFAP alone.

Interpretation

Currently available biomarkers reflect injury severity, and serum GFAP, measured within 24 h after injury, outperforms clinical characteristics in predicting CT abnormalities. Our results support the further development of serum GFAP assays towards implementation in clinical practice, for which robust clinical assay platforms are required.

Funding

CENTER-TBI study was supported by the European Union 7th Framework program (EC grant 602150).

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  • Rinnakkaistallenteet [19207]

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