# A narrow therapeutic window of platelet P2Y12 reactivity in high-risk Chinese percutaneous coronary intervention patients

**Authors:** Liying Gong, Yaxin Liu, Jingle Li, Shiming Tan, Chengxian Guo, Zhengmei Wang, Huiling Song, Yun Kuang, Yu Cao, Guoping Yang

PMC · DOI: 10.7717/peerj.20536 · PeerJ · 2026-01-09

## TL;DR

This study identifies a narrow range of platelet reactivity that minimizes both bleeding and ischemic risks in high-risk Chinese patients after heart procedures.

## Contribution

The study defines specific platelet reactivity thresholds for predicting ischemic and bleeding events in high-risk Chinese PCI patients.

## Key findings

- A VASP-PRI ≥ 0.45 predicts ischemic events with 86.6% sensitivity and 63.6% specificity.
- A VASP-PRI ≤ 0.24 predicts bleeding events with 72.1% sensitivity and 70.3% specificity.
- VASP-PRI is an independent predictor of major adverse cardiovascular events.

## Abstract

Much evidence has been provided that a therapeutic window of P2Y12receptor inhibition exists, which is highly significantly associated with ischemic and bleeding events. The therapeutic window for high-risk stratification after percutaneous coronary intervention (PCI) is lacking. We aimed to investigate the therapeutic window of P2Y12receptor inhibition in high-risk Chinese PCI patients.

In this observational study, we analyzed 860 high-risk patients who were undergoing PCI. The primary endpoint was the correlation between vasodilator-stimulated phosphoprotein platelet reactivity index (VASP-PRI) values with bleeding and ischemic components in high-risk patients. The secondary endpoint was a composite of cardiovascular death, myocardial infarction, definite stent thrombosis, urgent revascularization, and stroke at 12 months after the index procedure.

Among high-risk patients, VASP-PRI could significantly discriminate between PCI patients with and without ischemic events (area under the curve (AUC): 0.77; 95% CI [0.72–0.82]; P < 0.001). A VASP-PRI ≥ 0.45 was the optimal cutoff point to predict ischemic events (sensitivity: 86.6%; specificity: 63.6%). Similarly, VASP-PRI could also significantly discriminate between PCI patients with and without bleeding events ((AUC): 0.77; 95% CI [0.73–0.81]; P < 0.001). A VASP-PRI ≤ 0.24 was the optimal cutoff point to predict bleeding events (sensitivity: 72.1%; specificity: 70.3%). Multivariate analysis showed that VASP-PRI was an independent predictor of the risk of major adverse cardiovascular events (odds ratio: 10.67, 95% CI [3.78–30.08]).

Our results suggest that high-risk Chinese PCI patients have a narrow therapeutic window. Within this window, high-risk patients are at lower risk for both ischemic and bleeding events. Platelet reactivity may have significant implications for personalized antiplatelet therapy in high-risk patients.

## Linked entities

- **Proteins:** VASP (vasodilator stimulated phosphoprotein)
- **Diseases:** myocardial infarction (MONDO:0005068), stroke (MONDO:0005098)

## Full-text entities

- **Genes:** VASP (vasodilator stimulated phosphoprotein) [NCBI Gene 7408], P2RY12 (purinergic receptor P2Y12) [NCBI Gene 64805] {aka ADPG-R, BDPLT8, HORK3, P2T(AC), P2Y(12)R, P2Y(AC)}
- **Diseases:** stroke (MESH:D020521), ischemic (MESH:D002545), thrombosis (MESH:D013927), bleeding (MESH:D006470), death (MESH:D003643), myocardial infarction (MESH:D009203)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12794635/full.md

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Source: https://tomesphere.com/paper/PMC12794635