Startseite Cord blood S100B: reference ranges and interest for early identification of newborns with brain injury
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Cord blood S100B: reference ranges and interest for early identification of newborns with brain injury

  • Damien Bouvier EMAIL logo , Yves Giguère , Bruno Pereira , Nathalie Bernard , Isabelle Marc , Vincent Sapin und Jean-Claude Forest
Veröffentlicht/Copyright: 17. Oktober 2019
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Abstract

Background

Neurological complications are common in the premature and full-term neonates admitted to the intensive care unit, but the diagnosis of these complications is often difficult to make. S100B protein, measured in cord blood, may represent a valuable tool to better identify patients at risk of brain injury.

Methods

As a first step, we established S100B cord blood serum reference intervals from 183 preterm and 200 full-term neonates. We then measured cord blood serum S100B to identify neurological complications in 272 neonates hospitalized at the neonatal intensive care unit (NICU). Diagnosis of brain injury relied on imaging examination.

Results

The 95th percentiles of S100B concentration in cord blood were established as 1.21 μg/L for the 383 neonates, 0.96 μg/L for full-term neonates and 1.36 μg/L for premature neonates. Among the 272 neonates hospitalized at the NICU, 11 presented neurological complications. Using 1.27 μg/L as the optimal sensitivity/specificity threshold, S100B differentiate neonates with and without neurological complications with a sensitivity of 45.5% (95% confidence intervals [CI]: 16.7–76.6) and a specificity of 88.9% (95% CI: 84.4–92.4) (p = 0.006). In combination with arterial pH (<7.25), sensitivity increased to 90.9% (95% CI: 58.7–99.8), while specificity was 51.2% (95% CI: 44.8–57.7). The sensitivity is significantly (p = 0.03) increased in comparison to S100B alone. The specificity is significantly higher with S100B only than with pH + S100B (p < 0.001).

Conclusions

Cord blood S100B protein, in combination with arterial cord blood pH, has the potential to help clinicians to detect at birth neurological complications in neonates hospitalized in an NCIU.


Corresponding author: Damien Bouvier, MD, PhD, Service de Biochimie Médicale, Centre de Biologie, CHU Gabriel Montpied, 58 Rue Montalembert, 63000 Clermont-Ferrand, France; Biochemistry and Molecular Genetic Department, CHU Clermont-Ferrand, Clermont-Ferrand, France; and Université Clermont Auvergne, Faculty of Medicine, CNRS 6293, INSERM 1103, GReD, Clermont-Ferrand, France, Phone: +33 4 73 75 48 82, Fax: +33 4 73 75 18 55

Award Identifier / Grant number: NRFHPG-78880

Funding statement: This work was supported by the Canadian Institutes of Health Research (CIHR, Healthy Pregnancy Initiative from the Institute for Human Development, Child and Youth Health, Funder Id: http://dx.doi.org/10.13039/501100000031, Grant number: NRFHPG-78880). The authors thank Roche Diagnostics (Laval, Canada) for providing the s100 kits.

Acknowledgments

The authors thank the research nurses for the recruitment of participants and retrieval of data from the medical records and Alexandra Castillo for S100B dosages.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Employment or leadership: None declared.

  3. Honorarium: None declared.

  4. 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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Received: 2019-07-18
Accepted: 2019-09-30
Published Online: 2019-10-17
Published in Print: 2020-01-28

©2019 Walter de Gruyter GmbH, Berlin/Boston

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