# Platelet aggregation rate serves as a significant predictive indicator for thromboembolic events in the context of stent-assisted embolization for unruptured arterial aneurysms

**Authors:** Xiaopeng Huang, Tingbao Zhang, Yu Feng, Xiang Li, Kui Liu, Wenyuan Zhao

PMC · DOI: 10.3389/fneur.2025.1538753 · Frontiers in Neurology · 2025-05-01

## TL;DR

This study shows that measuring platelet aggregation rate can predict thromboembolic events in patients undergoing stent-assisted embolization for brain aneurysms.

## Contribution

The study introduces platelet aggregation rate as a novel predictive indicator for thromboembolic events in stent-assisted aneurysm treatment.

## Key findings

- Platelet aggregation rate (PAR) was significantly associated with thromboembolic events in patients undergoing stent-assisted embolization.
- A PAR cutoff value of 19.81 was identified as optimal for predicting thromboembolic risk.
- Using PAR and other indicators improved treatment outcomes compared to guideline-based empirical treatment.

## Abstract

Perioperative cerebrovascular thromboembolic events are serious complications of stent-assisted embolization (SAE) for unruptured intracranial aneurysms (UIAs). To date, there have been no definitive clinical trial results to effectively predict and prevent the occurrence of this complication. This study aims to elucidate the correlation between platelet aggregation rate (PAR) and thromboembolic events (TEs), with the goal of predicting the occurrence of cerebrovascular TEs in these patients.

In this retrospective, single-center cohort study, we included 704 cases of unruptured intracranial aneurysms treated with stent-assisted intervention from 2016 to 2020. Cerebrovascular TEs were defined as cerebral ischemic events occurring within 7 days before or after the interventional procedure. Light Transmission Aggregometry (LTA) was used to detect PAR in patients. Clinical data, including patients’ demographic information and perioperative PAR, were collected. Multivariate analysis was conducted to examine the correlation between these factors and the occurrence of TEs. Additionally, Lasso regression was employed to select clinical indicators associated with perioperative TEs. Receiver Operating Characteristic (ROC) curves were generated for prognostic indicators such as PAR, with the optimal cutoff value determined. A nomogram was then simulated, and predictive accuracy of the model was evaluated using Decision Curve Analysis (DCA).

A total of 562 patients were included in the final analysis. Significant differences were observed in the incidence of thrombosis between the control group and the experimental group (9.38% vs. 4.96%). The ROC curve of platelet aggregation index, highly correlated with prognosis and derived from Lasso regression, identified the optimal cutoff value for the maximum preoperative PAR as 19.81. A nomogram was constructed based on selected clinical baseline data, and its calibration was assessed using data from the prediction group. The net benefit of the experimental group model’s DCA curve was significantly improved.

For patients undergoing SAE for UIAs, utilizing PAR and other indicators as reference standards for treatment results in better prognosis compared to empirical treatment based on guidelines. Guiding antiplatelet therapy using PAR and other indicators is both meaningful and beneficial to clinical practice.

## Full-text entities

- **Genes:** CYP3A4 (cytochrome P450 family 3 subfamily A member 4) [NCBI Gene 1576] {aka CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4}, CYP2C19 (cytochrome P450 family 2 subfamily C member 19) [NCBI Gene 1557] {aka CPCJ, CYP2C, CYPIIC17, CYPIIC19, P450C2C, P450IIC19}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, JTB (jumping translocation breakpoint) [NCBI Gene 10899] {aka HJTB, HSPC222, PAR, hJT}
- **Diseases:** UIAs (MESH:D002532), drooping of the mouth (MESH:D009059), Weakness (MESH:D018908), seizures (MESH:D012640), cerebral infarction (MESH:D002544), thrombosis (MESH:D013927), SAE (MESH:D004617), gastric mucosa irritation (MESH:D013274), Aneurysm (MESH:D000783), cerebral ischemic (MESH:D002547), ischemic (MESH:D002545), neurological deficits (MESH:D009461), headache (MESH:D006261), bleeding (MESH:D006470), intracranial hemorrhage (MESH:D020300), cerebrovascular disease (MESH:D002561), aneurysm rupture (MESH:D017542), Platelet aggregation (MESH:D001791), intracranial bleeding (MESH:D013345), TEs (MESH:D013923), HLP (MESH:D006949), numbness (MESH:D006987), diabetes (MESH:D003920), Cerebrovascular infarction (MESH:D007238), trauma (MESH:D014947), ICH (MESH:D002543), vomiting (MESH:D014839), Loss or blurred vision (MESH:D014786), stroke (MESH:D020521), hematologic disorders (MESH:D006402), Hypertension (MESH:D006973), systemic diseases (MESH:D034721), Altered consciousness (MESH:D003244), Dizziness (MESH:D004244)
- **Chemicals:** arachidonic acid (MESH:D016718), AA (-), aspirin (MESH:D001241), adrenaline (MESH:D004837), ticagrelor (MESH:D000077486), ADP (MESH:D000244), omeprazole (MESH:D009853), lipid (MESH:D008055), lansoprazole (MESH:D064747), TXA2 (MESH:D013928), TG (MESH:D014280), Clopidogrel (MESH:D000077144), silicon (MESH:D012825), cholesterol (MESH:D002784), alcohol (MESH:D000438)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs12248560, rs4986893, rs4244285

## Full text

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## Figures

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## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12078147/full.md

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Source: https://tomesphere.com/paper/PMC12078147