# Serum iron as a biomarker for “penumbra freezing” in patients with acute ischemic stroke

**Authors:** Xianwen Zhang, Zhiyao Xu, Linyan Li, Huimin Deng, Qiang Zhou, Jianyu Liu, Hua Liu

PMC · DOI: 10.3389/fnins.2025.1764523 · Frontiers in Neuroscience · 2026-01-12

## TL;DR

Low serum iron levels may help identify stroke patients who could benefit from late reperfusion therapy.

## Contribution

Serum iron is proposed as a novel biomarker for 'penumbra freezing' in late-presenting stroke patients.

## Key findings

- PF group had significantly lower serum iron levels than APF group.
- Adjusted model showed improved diagnostic accuracy with an AUC of 0.76.

## Abstract

Identifying salvageable penumbra is crucial for revascularization in acute ischemic stroke (AIS) patients presenting beyond standard therapeutic windows. Dysregulated iron metabolism and ferroptosis play significant roles in the pathophysiology of cerebral ischemia. This study aimed to investigate serum iron as a biomarker for identifying the “penumbra freezing” (PF) phenomenon in AIS patients who present beyond the conventional time window.

This study included patients with AIS presenting late (beyond 4.5-h treatment window). Participants were classified into PF and absence of PF (APF) groups based on CT perfusion and EXTEND trial criteria. Multivariable regression analyzed associations with PF, and diagnostic accuracy was evaluated via ROC curves.

A total of 141 AIS patients were finally included (Age: 71.16 ± 12.37, 54% male). Serum iron levels were significantly lower in the PF group compared with the APF group (8.59 ± 4.34 μmol/L vs. 11.54 ± 6.37 μmol/L, p = 0.04). The initial ROC analysis yielded an AUC of 0.63 (95% CI: 0.48–0.79, p = 0.09). After adjustment for confounders, the model’s AUC improved significantly to 0.76 (95% CI: 0.63–0.89, p < 0.01).

Serum iron levels correlate with the PF phenomenon in AIS patients beyond the time window, potentially serving as an auxiliary biomarker to aid in identifying suitable candidates for delayed reperfusion therapy. This indicator offers convenient and rapid detection with clinical translation potential, though further validation in prospective, multicenter, large-scale studies remains necessary.

## Full-text entities

- **Diseases:** APF (MESH:D004832), AIS (MESH:D000083242), cerebral ischemia (MESH:D002545)
- **Chemicals:** iron (MESH:D007501)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

48 references — full list in the complete paper: https://tomesphere.com/paper/PMC12832780/full.md

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Source: https://tomesphere.com/paper/PMC12832780