# Prognostic Value of Serum S100B Protein for Neurological Outcomes After Cardiac Arrest: A Systematic Review and Meta-Analysis

**Authors:** Łukasz Szpinda, Michal Lis, Michal Pruc, Weronika Goraj, Iwona Niewiadomska, Maciej Maslyk, Katarzyna Kotfis, Hanno L. Tan, Enrico Baldi, Lukasz Szarpak

PMC · DOI: 10.3390/jcm15010238 · Journal of Clinical Medicine · 2025-12-28

## TL;DR

This study finds that the protein S100B in blood can predict brain outcomes after cardiac arrest, helping doctors make better decisions.

## Contribution

This is the first systematic review and meta-analysis confirming S100B's reliability as an early biomarker for neurological prognosis after cardiac arrest.

## Key findings

- Lower S100B levels were strongly associated with better neurological outcomes after cardiac arrest.
- S100B showed high diagnostic accuracy with a pooled sensitivity of 0.63 and specificity of 0.93.
- Findings were consistent across different populations and time points, with minimal publication bias.

## Abstract

Background/Objectives: Cardiac arrest (CA) continues to be one of the leading causes of mortality and long-term neurological disability worldwide. Accurate early neuroprognostication after return of spontaneous circulation is essential for guiding post-resuscitation care. The calcium-binding astrocytic protein S100B has been identified as a potential biomarker for hypoxic–ischemic brain injury. This systematic review and meta-analysis assessed the prognostic and diagnostic efficacy of serum S100B in forecasting neurological outcomes after CA. Methods: Thorough searches of PubMed, Embase, Scopus, Web of Science, CENTRAL, and CINAHL from their inception to November 2025 uncovered 40 observational studies. Results: Pooled analyses employing random-effects models revealed markedly reduced S100B concentrations in patients with favourable neurological outcomes compared to those with unfavourable outcomes (standardized mean difference −1.78, 95%CI: −2.25 to −1.31; p < 0.001). The diagnostic accuracy was high, with pooled sensitivity and specificity of 0.63 and 0.93, respectively, and an area under the curve of 0.89 (95% CI 0.85–0.92). Subgroup and sensitivity analyses confirmed the robustness of these findings across various study populations and temporal points, with negligible evidence of publication bias. Conclusions: These results indicate that serum S100B is a reliable early biomarker of neurological prognosis after CA. Incorporating S100B into multimodal predictive frameworks may enhance post-resuscitation decision-making.

## Linked entities

- **Proteins:** S100B (S100 calcium binding protein B)
- **Diseases:** cardiac arrest (MONDO:0000745)

## Full-text entities

- **Genes:** S100B (S100 calcium binding protein B) [NCBI Gene 6285] {aka NEF, S100, S100-B, S100beta}
- **Diseases:** CA (MESH:D006323), hypoxic-ischemic brain injury (MESH:D020925), neurological disability (MESH:D009069)
- **Chemicals:** calcium (MESH:D002118)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC12786873/full.md

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Source: https://tomesphere.com/paper/PMC12786873