# The predictive role of protease-activated receptor (PAR-1) polymorphisms and activated microplatelets on the severity of atherosclerosis – preliminary studies

**Authors:** Urszula Jakobsche-Policht, Agnieszka Bronowicka-Szydełko, Rajmund Adamiec, Dorota Bednarska-Chabowska, Łukasz Lewandowski, Rafał Małecki, Kinga Gostomska-Pampuch, Joanna Adamiec-Mroczek, Marta Myszka-Kozłowska, Dagmara Baczyńska, Maciej Rabczyński, Edwin Kuźnik, Jacek Polański, Helena Martynowicz, Daria Dolińska, Paulina Matlak, Julia Sobczyńska, Maciej Ziomek, Maciej Tota, Wojciech Stach, Katarzyna Madziarska

PMC · DOI: 10.3389/fmolb.2025.1662954 · Frontiers in Molecular Biosciences · 2026-01-16

## TL;DR

This study explores how PAR-1 gene variations and activated microplatelets influence the severity of atherosclerosis in diabetes and atherosclerosis obliterans.

## Contribution

The study identifies specific PAR-1 polymorphisms and PMP activity as potential predictors of atherosclerosis severity.

## Key findings

- The −506D/D and IVS-14A/A PAR-1 polymorphisms are more common in diabetic macroangiopathy.
- The −506I/D polymorphism is more frequent in atherosclerosis obliterans and may be protective.
- Increased PMP activity in diabetes contributes to atherosclerosis progression.

## Abstract

This study is a comprehensive analysis of PAR-1 – involved in thrombin interaction with platelets (PLT), present on PLT and microparticles (PMP) – to understand its role in diabetic macroangiopathy (DM) and atherosclerosis obliterans (AO). The applied RT-PCR, aggregometry, flow cytometry, a proprietary method for PMP level determination, ELISA, and multidimensional statistical analysis allowed for the determination of: PAR-1 activation levels, its polymorphisms, PLT/PMP aggregation capacity, hemostatic factors, and their interrelationships. In DM, the −506D/D and IVS-14A/A polymorphisms were significantly more frequent, whereas the −506I/D was much more common in AO, suggesting the protective properties of the I allele and its potential significance as a prognostic factor for a milder course of atherosclerosis. Similarly, increased PMP activity in DM indicates that activated PMP contribute to the atherosclerosis progression. A probable explanation for the reduced PAR-1 activation in AO is its association with the observed lower levels of von Willebrand factor. Interaction analysis showed that although the percentage of PMP did not affect the odds of AO (among AO and DM), at high PMP percentages, increased PAR-1 activation became a factor elevating the AO odds. Quantitative assessment of PAR-1 and PMP allows for predicting the severity of atherosclerosis.

## Linked entities

- **Genes:** MARK2 (microtubule affinity regulating kinase 2) [NCBI Gene 2011]
- **Diseases:** atherosclerosis (MONDO:0005311)

## Full-text entities

- **Genes:** F2R (coagulation factor II thrombin receptor) [NCBI Gene 2149] {aka CF2R, HTR, PAR-1, PAR1, TR}, F2 (coagulation factor II, thrombin) [NCBI Gene 2147] {aka PT, RPRGL2, THPH1}, VWF (von Willebrand factor) [NCBI Gene 7450] {aka F8VWF, VWD}
- **Diseases:** DM (MESH:D003920), AO (MESH:D050197)
- **Mutations:** IVS-14A/A

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12856924/full.md

## References

74 references — full list in the complete paper: https://tomesphere.com/paper/PMC12856924/full.md

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Source: https://tomesphere.com/paper/PMC12856924