# Protein Z and Protein Z Complex in the Acute Phase of Ischemic Stroke: Potential Markers of Coagulation and Prognostic Value in Patients Treated with Thrombolysis or Conservative Therapy

**Authors:** Małgorzata Wiszniewska, Urszula Włodarczyk, Mariusz Domagalski, Artur Słomka, Inga Dziembowska, Maciej Gawrysiak, Anna Żdanowicz, Ewa Żekanowska

PMC · DOI: 10.3390/neurolint18020029 · Neurology International · 2026-02-06

## TL;DR

This study explores how Protein Z and its complex relate to coagulation and outcomes in ischemic stroke patients treated with thrombolysis or conservative therapy.

## Contribution

The study identifies Protein Z concentration differences in stroke patients based on treatment and dyslipidemia status, suggesting potential prognostic value.

## Key findings

- PZ concentrations were significantly higher in thrombolysis-treated patients compared to conservatively managed patients on both day 1 and day 7.
- A slight negative correlation between PZ and mRS was observed in conservatively treated patients on day 7.
- PZ levels increased in thrombolysis-treated patients with dyslipidemia but decreased in those without.

## Abstract

Background/Objectives: Protein Z (PZ) and the protein Z-dependent protease inhibitor (ZPI) are vitamin K-dependent regulators of coagulation that inhibit activated factor Xa. Their relevance in ischemic stroke (IS) remains insufficiently characterized, with inconsistent evidence regarding their association with stroke severity and outcomes. This study aimed to evaluate the concentrations and dynamics of PZ and ZPI in the acute phase of IS in patients treated with intravenous thrombolysis or conservative therapy and to assess their potential prognostic significance. Methods: Eighty-four patients with acute IS were enrolled and divided into two groups: group I treated with intravenous thrombolysis (rt-PA) and group II managed conservatively. PZ and ZPI concentrations were measured using ELISA on admission (day 1) and on day 7. Associations with factor X activity, the modified Rankin Scale (mRS), and the National Institutes of Health Stroke Scale (NIHSS) were analyzed using nonparametric tests and Spearman correlations (p < 0.05). Results: PZ concentrations were significantly higher in thrombolysis-treated patients than in conservatively managed patients both on day 1 (median: 2810.05 vs. 2178.50 ng/mL; p = 0.024) and day 7 (2982.90 vs. 2286.50 ng/mL; p = 0.026). A slight negative correlation between PZ and mRS on day 7 was observed in the conservative group (r = −0.360; p = 0.043). In thrombolysis-treated patients with dyslipidemia, PZ increased from day 1 to day 7, whereas it decreased in those without dyslipidemia. No significant correlations were found between PZ, ZPI, or factor X and NIHSS or ASTRAL scores. Conclusions: Higher PZ concentrations in the acute phase of IS—particularly in rt-PA-treated patients—may reflect differences related to the timing of the acute ischemic process and reperfusion status, suggesting potential utility as markers of stroke severity or outcome.

## Linked entities

- **Proteins:** SERPINA10 (serpin family A member 10)
- **Diseases:** ischemic stroke (MONDO:1060198), dyslipidemia (MONDO:0002525)

## Full-text entities

- **Genes:** PLG (plasminogen) [NCBI Gene 5340] {aka HAE4}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, PLAT (plasminogen activator, tissue type) [NCBI Gene 5327] {aka T-PA, TPA}, SERPINA10 (serpin family A member 10) [NCBI Gene 51156] {aka PZI, ZPI}, F10 (coagulation factor X) [NCBI Gene 2159] {aka FX, FXA}, F3 (coagulation factor III, tissue factor) [NCBI Gene 2152] {aka CD142, TF, TFA}
- **Diseases:** Stroke (MESH:D020521), hemorrhagic (MESH:D006470), AIS (MESH:D000083242), small-vessel disease (MESH:D059345), NIHSS (MESH:C538175), dyslipidemia (MESH:D050171), injury to (MESH:D014947), cardioembolic (MESH:D000083262), vessel occlusion (MESH:C536223), TACI (MESH:D020520), ischemic (MESH:D002545), diabetes mellitus (MESH:D003920), lacunar infarction (MESH:D059409), atherosclerotic plaque (MESH:D058226), atherosclerotic (MESH:D050197), hypertension (MESH:D006973), thrombus (MESH:D013927), IS (MESH:D002544), atrial fibrillation (MESH:D001281), blood coagulation (MESH:D001778)
- **Chemicals:** phospholipids (MESH:D010743), ASA (MESH:D001241), cholesterol (MESH:D002784), triglycerides (MESH:D014280), lipid (MESH:D008055), Z (MESH:C000597310), calcium (MESH:D002118), vitamin K (MESH:D014812)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** G79A

## Full text

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## References

22 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943381/full.md

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Source: https://tomesphere.com/paper/PMC12943381