# Four new markers of early thrombotic molecules and thromboelastography in prognostic evaluation of AMI patients undergoing PCI

**Authors:** Weisha Sun, Yi Gao, Weiran Sun, Qinhan Zhang, Xi Zhao, Xuan Jing, Chonghua Hao

PMC · DOI: 10.1186/s43044-026-00728-5 · The Egyptian Heart Journal · 2026-03-11

## TL;DR

This paper explores new biomarkers and thromboelastography to improve diagnosis and prognosis of heart attack patients undergoing a specific treatment.

## Contribution

The study introduces four new thrombotic biomarkers and evaluates thromboelastography for enhanced risk assessment in AMI patients.

## Key findings

- The biomarkers TM, TAT, PIC, and t-PAIC reflect endothelial injury and coagulation processes in AMI patients.
- Thromboelastography (TEG) provides dynamic monitoring of coagulation, aiding individualized antiplatelet therapy.

## Abstract

Early and accurate diagnosis and prognostic evaluation of acute myocardial infarction (AMI) are essential to improve clinical outcomes. Conventional coagulation tests (CCTs) are routinely used but have limited sensitivity and specificity in capturing the complexity of thrombus formation and fibrinolysis.

Recent research has introduced a range of emerging biomarkers—including thrombomodulin, thrombin–antithrombin complex, plasmin–α2-plasmin inhibitor complex, and tissue plasminogen activator inhibitor complex—that reflect endothelial injury, thrombin generation, and fibrinolytic activity. In parallel, thromboelastography (TEG) has gained attention as a whole-blood assay that offers a dynamic and comprehensive view of the coagulation cascade. These new tools provide valuable information beyond that available from traditional tests and have been explored for their diagnostic and prognostic utility in AMI patients undergoing percutaneous coronary intervention. The combined assessment of these biomarkers and TEG parameters enhances risk stratification by reflecting both vascular injury and coagulation dysfunction. Furthermore, TEG supports individualized antiplatelet therapy by continuously monitoring clot formation, strength, and dissolution.

Based on the available evidence, we conclude that the biomarkers—TM, TAT, PIC, and t-PAIC—demonstrate potential clinical value in providing a more refined assessment of thrombus formation and fibrinolytic activity and TEG provides an important basis for optimizing antiplatelet therapy by dynamically monitoring the coagulation process in whole blood.

## Linked entities

- **Diseases:** acute myocardial infarction (MONDO:0004781)

## Full-text entities

- **Genes:** THBD (thrombomodulin) [NCBI Gene 7056] {aka AHUS6, BDCA-3, BDCA3, CD141, THPH12, THRM}, PLG (plasminogen) [NCBI Gene 5340] {aka HAE4}, SERPINC1 (serpin family C member 1) [NCBI Gene 462] {aka AT3, AT3D, ATIII, ATIII-R2, ATIII-T1, ATIII-T2}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}
- **Diseases:** thrombotic (MESH:D013927), AMI (MESH:D009203), coagulation (MESH:D001778), endothelial injury (MESH:D057772)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12979761/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12979761/full.md

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Source: https://tomesphere.com/paper/PMC12979761