Preview

Pharmacogenetics and Pharmacogenomics

Advanced search

The role of single nucleotide polymorphisms in predicting individual stroke risk

https://doi.org/10.37489/2588-0527-0008

EDN: BQRZEP

Abstract

Background. In the context of predictive medicine, personalized assessment of ischemic stroke risk based on molecular genetic testing is becoming increasingly relevant. Polymorphisms in folate cycle genes (MTHFR, MTR, MTRR), leading to hyperhomocysteinemia, cause endothelial dysfunction and accelerate atherogenesis. The role of the renin-angiotensin system (RAS) is no less important: genetic variations in the AGT and NOS3 genes are associated with arterial hypertension and altered vascular tone, which creates a predisposition to cerebrovascular accidents.

Objective. To identify associations between polymorphisms of folate cycle and renin-angiotensin system genes and the development of acute ischemic stroke and transient ischemic attack (TIA).

Methods. The observational study included 492 patients who were treated in hospital at the Institution Clinical Hospital No. 1 of the Presidential Administration of the Russian Federation in the period 2022–2025 and who signed informed consent for molecular genetic testing. A comparative analysis of clinical, laboratory, instrumental, and molecular genetic data (polymorphisms of MTHFR, MTR, MTRR, AGT, NOS3, and AGTR1) was performed between the ischemic stroke group (n=426) and the TIA group (n=66). Statistical analysis was carried out using the Mann-Whitney U test and Pearson's chisquared test.

Results. Stroke patients were older (73 vs 66 years, p=0.005) and more frequently male (43.4 % vs 27.3 %, p=0.013). The stroke group had significantly higher triglyceride levels (p < 0.001) and potassium levels (p < 0.001), as well as a higher frequency of pathological MRT findings (p < 0.001). Genetic analysis revealed a significant predominance in the stroke group of homozygous CC genotypes for MTHFR C677T (p=0.001), AGT174 (p=0.004), AGT235 (p < 0.001), and NOS3 (p=0.028). In contrast, the TIA group more frequently carried TT genotypes for C677T AGT235, and NOS3, as well as the heterozygous CT genotype for AGT174.

Conclusion. Molecular genetic testing of polymorphisms in folate cycle and renin — angiotensin system genes represents a promising tool for risk stratification and differential diagnosis of ischemic stroke versus TIA, and may serve as a foundation for personalized pharmacotherapy in the nearest future.

About the Authors

N. A. Kovtun
Clinical Hospital № 1 of Department of President Affairs; Central State Medical Academy of Department of President Affairs
Russian Federation

Natalia A. Kovtun — Cand. Sci. (Med.), Head of Laboratory at Clinical Hospital No. 1 of the Presidential Administration of the Russian Federation, and Associate Professor of the Department of Healthcare Organization and Public Health, Medical Insurance, and State Control in Healthcare at the Central State Medical Academy of the Presidential Administration of the Russian Federation

Moscow



Т. V. Isaeva
Clinical Hospital № 1 of Department of President Affairs
Russian Federation

Tatyana V. Isaeva — Cand. Sci. (Med.), Head of the Medical Rehabilitation Center

Moscow



M. I. Savelyeva
Yaroslavl State Medical University
Russian Federation

Marina I. Savelyeva — Dr. Sci. (Med.), Professor, Professor of the Department of Therapy named after Professor E. N. Dormidontov

Yaroslavl



V. V. Boyarintsev
Central State Medical Academy of Department of President Affairs
Russian Federation

Valery V. Boyarintsev — Dr. Sci. (Med.), Professor, Professor of the Russian Academy of Sciences, Head of the Department of Emergency Care, Urgent and Extreme Medicine

Moscow



References

1. Dutova T. I., Banin I. N., Ermolenko N. A. Genetic passport as a basis for primary and secondary prevention of cerebral infarction in young people. Lechaschi Vrach. 2023; 7-8 (26): 45-51. (In Russ.).

2. Dichgans M, Beaufort N, Debette S, Anderson CD. Stroke Genetics: Turning Discoveries into Clinical Applications. Stroke. 2021 Aug;52(9):2974- 2982. doi: 10.1161/STROKEAHA.121.032616.

3. Chugunova S.A., Nikolaeva T.Ya., Ignatieva A.V., Popov M.M. Genetic risk factors of thrombofilia in a young ischemic stroke patient (clinical case report). Yakut Medical Journal. 2017;(3):65-68. (In Russ.).

4. Temprano-Sagrera G, Sitlani CM, Bone WP, et al. Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. J Thromb Haemost. 2022 Jun;20(6):1331-1349. doi: 10.1111/jth.15698.

5. Drozdova EL, Komkova GV, Polonikova AA, et al. Relationship between polymorphism rs1546155 of the GGT7 gene and the risk of ischemic stroke. Research Results in Biomedicine. 2024;10(3):339- 350. (In Russ.).

6. Tsalta-Mladenov M, Levkova M, Andonova S. Factor V Leiden, Factor II, Protein C, Protein S, and Antithrombin and Ischemic Strokes in Young Adults: A Meta-Analysis. Genes (Basel). 2022 Nov 9;13(11):2081. doi: 10.3390/genes13112081.

7. Shibeeb S, Al-Rayashi N, Shams N, et al. Factor V Leiden (R506Q), Prothrombin G20210A, and MTHFR C677T Variants and Thrombophilia in Qatar Biobank Participants: A Case Control Study. Pathophysiology. 2024 Oct 21;31(4):608- 620. doi: 10.3390/pathophysiology31040044.

8. Ni J, Zhang L, Zhou T, et al. Association between the MTHFR C677T polymorphism, blood folate and vitamin B12 deficiency, and elevated serum total homocysteine in healthy individuals in Yunnan Province, China. J Chin Med Assoc. 2017 Mar;80(3):147-153. doi: 10.1016/j.jcma.2016.07.005.

9. Huang X, Ye Q, Zhang Y, et al. Effects of eNOS rs1799983 and DYRK1A rs720470 on Susceptibility to Ischemic Stroke and its Subtypes: A Prospective Observational Study. Clin Appl Thromb Hemost. 2025 Jan-Dec;31:10760296251384918. doi: 10.1177/10760296251384918.

10. Clinical guidelines: Ischemic stroke and transient ischemic attack. https://cr.minzdrav.gov.ru/previewcr/814_1 Russian

11. Meng H, Huang S, Yang Y, et al. Association Between MTHFR Polymorphisms and the Risk of Essential Hypertension: An Updated Meta-analysis. Front Genet. 2021 Nov 26;12:698 590. doi: 10.3389/fgene.2021.698590.

12. Chang G, Kuai Z, Wang J, et al. The association of MTHFR C677T variant with increased risk of ischemic stroke in the elderly population: a meta-analysis of observational studies. BMC Geriatr. 2019 Nov 27;19(1):331. doi: 10.1186/s12877-019-1304-y.

13. Isordia-Salas I, Santiago-Germán D, Cerda-Mancillas MC, et al. Gene polymorphisms of angiotensin-converting enzyme and angiotensinogen and risk of idiopathic ischemic stroke. Gene. 2019 Mar 10;688:163-170. doi: 10.1016/j.gene.2018.11.080.

14. Jalel A, Midani F, Fredj SH, et al. Association of BglII Polymorphism in ITGA2 and (894G/T and -786T/C) Polymorphisms in eNOS Gene With Stroke Susceptibility in Tunisian Patients α2 Gene Polymorphism in α2β1 Integrin and eNOS Gene Variants and Stroke. Biol Res Nurs. 2021 Jul;23(3):408-417. doi: 10.1177/1099800420977685.

15. Kumar A, Sharma R, Misra S, et al. Relationship between methylenetetrahydrofolate reductase (MTHFR) gene (A1298C) polymorphism with the risk of stroke: A systematic review and meta-analysis. Neurol Res. 2020 Nov;42(11):913- 922. doi: 10.1080/01616412.2020.1798107.


Review

For citations:


Kovtun N.A., Isaeva Т.V., Savelyeva M.I., Boyarintsev V.V. The role of single nucleotide polymorphisms in predicting individual stroke risk. Pharmacogenetics and Pharmacogenomics. 2026;(2):24-34. (In Russ.) https://doi.org/10.37489/2588-0527-0008. EDN: BQRZEP

Views: 57

JATS XML


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 2588-0527 (Print)
ISSN 2686-8849 (Online)