# Application of Serum NADPH Oxidase 2 Levels for Predicting 180‐Day Clinical Outcomes Following Severe Traumatic Brain Injury: A Prospective Cohort Analysis

**Authors:** Chang Su, Dapu Shen, Junlong Xu, Miaomiao Chen, Heng He, Jianping Ye

PMC · DOI: 10.1002/brb3.70692 · Brain and Behavior · 2025-07-11

## TL;DR

This study shows that measuring NOX2 in blood can help predict outcomes for severe traumatic brain injury patients over 180 days.

## Contribution

The study identifies serum NOX2 as a novel biomarker for predicting sTBI outcomes.

## Key findings

- sTBI patients had higher serum NOX2 levels than healthy controls.
- Serum NOX2 levels predicted 180-day mortality and poor prognosis.
- Combining NOX2 with GCS and CT scores improved outcome prediction.

## Abstract

Nicotinamide adenine dinucleotide phosphate oxidase 2 (NOX2) affects oxidative response to acute brain injury. We set out to determine if there are connections between serum NOX2 levels, severity, and subsequent clinical outcomes of severe traumatic brain injury (sTBI).

In this prospective cohort study, serum NOX2 levels were measured in 123 patients and 123 controls. The Glasgow Coma Scale (GCS) scores and Rotterdam computed tomography (CT) classifications were applied for assessing injury severity. A poor prognosis was considered if the Glasgow Outcome Scale Extended (GOSE) score was 4 or below at 180 days post‐injury.

STBI patients exhibited markedly enhanced serum NOX2 levels relative to healthy controls, and serum NOX2 levels were independently linked to Rotterdam CT classifications and GCS scores. Serum NOX2 levels effectively identified individuals at risk of death or poor prognosis at 180‐day after sTBI. When compared to GCS scores and Rotterdam CT classifications, its predictive power was comparable. When the three variables were utilized together, the model's predictive ability was significantly higher than when they were independently used.

NOX2 might be used as a potential biomarker to assess the severity of sTBI and foretell its outcome, since elevated serum NOX2 levels are significantly linked to increasing severity, 180‐day mortality, and poor prognosis after sTBI.

This prospective cohort study found that serum NOX2 levels were closely related to the disease severity of sTBI patients and could predict the 180‐day mortality and poor prognosis of the patients.

## Linked entities

- **Proteins:** CYBB (cytochrome b-245 beta chain)
- **Diseases:** traumatic brain injury (MONDO:0858950)

## Full-text entities

- **Genes:** CYBB (cytochrome b-245 beta chain) [NCBI Gene 1536] {aka AMCBX2, CGD, CGDX, GP91-1, GP91-PHOX, GP91PHOX}
- **Diseases:** sTBI (MESH:D045169), death (MESH:D003643), Traumatic Brain Injury (MESH:D000070642), brain injury (MESH:D001930)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

14 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12246553/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12246553/full.md

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Source: https://tomesphere.com/paper/PMC12246553