Prevalence of polymorphism of АDRВ1, AGT, SOD2, CAT genes and their combinations to assess the risk of developing cardiovascular disease
- Authors: Golovanova N.E.1,2, Astratenkova I.V.1, Lukyanova I.Y.1,2, Basanko A.V.3
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Affiliations:
- Saint Petersburg State University
- North-Western State Medical University named after I.I. Меchnikov
- Thumbay University Hospital
- Issue: Vol 28, No 1 (2024)
- Pages: 35-41
- Section: Original studies
- URL: https://journals.eco-vector.com/RFD/article/view/624814
- DOI: https://doi.org/10.17816/RFD624814
- ID: 624814
Cite item
Abstract
BACKGROUND: Cardiovascular disease remains a major public health problem associated with high mortality. The development of these diseases is associated with many genetic and cardiovascular risk factors, so the study of a person’s genetic predisposition to the development of cardiovascular disease based on gene polymorphism remains actual. The aim of research was to study the combination of polymorphisms of the ADRB1 rs1801253, AGT rs4762, SOD2 rs4880 and CAT rs1001179 genes in healthy young people to assess individual genetic predisposition to the development of cardiovascular disease.
MATERIALS AND METHODS: The study involved 33 people aged 19 to 21 years who currently had no pathology of the cardiovascular system. DNA was isolated from oral epithelial cells. Genotyping of DNA samples was determined using real-time polymerase chain reaction.
RESULTS: Among those examined, 39.4% had one or two unfavorable alleles for the ADRB1, AGT genes, suggesting a genetic predisposition to the development of cardiovascular disease. Unfavorable alleles of the ADRB1 gene were more common compared to the AGT gene. Each of those examined at risk of developing cardiovascular disease had one or two alleles associated with a decrease in the functioning of enzymes of the antioxidant system. Of the 33 people, only four (12.1%) do not have an unfavorable allele for the SOD2 and CAT genes.
CONCLUSIONS: We believe that the determination of polymorphisms in genes for enzymes of the antioxidant system will be an important additional criterion for earlier and more active prevention of cardiovascular disease.
Keywords
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About the authors
Natalya E. Golovanova
Saint Petersburg State University; North-Western State Medical University named after I.I. Меchnikov
Email: nesh1764@mail.ru
ORCID iD: 0000-0001-9286-8787
SPIN-code: 9598-4184
Cand. Sci. (Biol.), Assistant Professor
Russian Federation, Saint Petersburg; Saint PetersburgIrina V. Astratenkova
Saint Petersburg State University
Email: astratenkova@mail.ru
ORCID iD: 0000-0003-0533-1098
SPIN-code: 5045-2305
Cand. Sci. (Biol.), Assistant Professor
Russian Federation, Saint PetersburgIrina Yu. Lukyanova
Saint Petersburg State University; North-Western State Medical University named after I.I. Меchnikov
Email: irina.loukianova@yahoo.com
ORCID iD: 0000-0001-5124-1953
SPIN-code: 5325-8354
MD, Dr. Sci. (Med.), Professor
Russian Federation, Saint Petersburg; Saint PetersburgAleksandra V. Basanko
Thumbay University Hospital
Author for correspondence.
Email: aleksandra.basanko@gmail.ru
ORCID iD: 0009-0002-1213-5861
SPIN-code: 2738-5341
MD
United Arab Emirates, AjmanReferences
- Otaki Y, Watanabe T, Nishiyama S, et al. The impact of superoxidedismutase-1 geneticvariationon cardiovascular and all-cause mortality in a prospective cohort study: The Yamagata (Takahata) Study. PLoS One. 2016;11(10):e0164732. doi: 10.1371/journal.pone.0164732
- Afanasiev SA, Rebrova TYu, Muslimova EF, Borisova EV. Association of polymorphic variants of ADRB1 gene with contractile myocardial dysfunction and erythrocyte adrenoreactivity in patients with rhythm disorders. Russian Journal of Cardiology. 2019;24(7):47–52. EDN: MCERZV doi: 10.15829/1560-4071-2019-7-47-52
- Garganeeva AA, Aleksandrenko VА, Kuzheleva EA, et al. Association of beta-adrenergic reactivity index of erythrocyte membranes in myocardial infarction with genetic features of the beta-adrenoreceptor apparatus. South Russian Journal of Therapeutic Practice. 2021;2(1):32–39. EDN: HPHXPO doi: 10.21886/2712-8156-2021-2-1-32-39
- Elkina AYu, Akimova NS, Shvarts YuG. Polymorphism of ACE, AGT, AGTR1 genes as genetic predictors of hypertension. Russian Journal of Cardiology. 2021;26(S1):35–40. EDN: SCHTRS doi: 10.15829/1560-4071-2021-4143
- Larina VN, Leonova MV. Genetic polymorphism of beta1-adrenergic receptors and the effect on the clinical efficacy of beta-adrenoblockers. Rational Pharmacotherapy in Cardiology. 2021;17(5):752–760. EDN: WFIMRJ doi: 10.20996/1819-6446-2021-10-13
- Bruck H, Leineweber K, Temme T, et al. The Arg389Gly beta1-adrenoceptor polymorphism and catecholamine effects on plasma-renin activity. JACC. 2005;46(11):2111–2116. doi: 10.1016/j.jacc.2005.08.041
- Shahid M, Rehman K, Akash MSH, et al. Genetic polymorphism in angiotensinogen and its association with cardiometabolic diseases. Metabolites. 2022;12(12):1291–1305. doi: 10.3390/metabo12121291
- Ponasenko AV, Sinitsky MY, Khutornaya MV. Molecular genetic markers of atrial fibrillation. Bulletin of Siberian Medicine. 2020;19(1):180–189. EDN: VJQCKL doi: 10.20538/1682-0363-2020-1-180-189
- Komissarova SM, Nyazova SS, Chakova NN, Krasko OV. Polymorphic variants of genes coding sympathoadrenal system influence on phenotype of patients with hypertrophic cardiomyopathy. Russian Journal of Cardiology. 2015;20(6):75–80. EDN: TZIYHB doi: 10.15829/1560-4071-2015-05-75-80
- Babenko AY, Kostareva AA, Grineva EN, et al. The contribution of the common single-nucleotide polymorphisms of β1-adrenoreceptor gene to cardiovascular alteration in patients with thyrotoxicosis. Clinical and experimental thyroidology. 2014;10(2):22–31. EDN: SKXCXX doi: 10.14341/CET201410222-31
- Li YY, Wang H, Wang H, Zhang YY. Myocardial infarction and AGT p.Thr174Met polymorphism: a meta-analysis of 7657 subjects. Cardiovasc Ther. 2021;2021:6667934. doi: 10.1155/2021/6667934
- Koziolova NA, Chernyavina AI. The contribution of the AGT, GNB3, MTHFR, MTRR, ApoE, and PPARα polymorphisms to the development of masked arterial hypertension in patients with low and moderate cardiovascular risk. Almanac of Clinical Medicine. 2021;49(2):142–148. doi: 10.18786/2072-0505-2021-49-027
- Zheykova TV, Golubenko MV, Buikin SV, et al. Association of Ala16Val polymorphism in superoxide dismutase 2 gene (SOD2) with coronary arthery disease in the male Russian population. The Siberian Journal of Clinical and Experimental Medicine. 2012;27(4):34–37. EDN: QBFPON
- Bereza IA, Amromina AM, Shaikhova DR, et al. Relationship of the superoxide dismutase 2 (SOD2) gene Ala16Val polymorphism with risk factors for the cardiovascular disease in iron and steel production employees. Hygiene and Sanitation. 2023;102(5):457–461. EDN: PPESVO doi: 10.47470/0016-9900-2023-102-5-457-461
- Sousa T, Oliveira S, Afonso J, et al. Role of H2O2 in hypertension, renin-angiotensin system activation and renal medullary disfunction caused by angiotensin II. Br J Pharmacol. 2012;166(8):2386–2401. doi: 10.1111/j.1476-5381.2012.01957.x
- Nadif R, Mintz M, Jedlicka A, et al. Association of CAT polymorphisms with catalase activity and exposure to environmental oxidative stimuli. Free Radic Res. 2005;39(12):1345–1350. doi: 10.1080/10715760500306711
- Kolesnikova LI, Bairova TA, Pervushina OA. Frequency of polymorphism of Ala16Val gene SOD2 in samples of Mongoloid and Caucasoid population, living in Eastern Siberia. Acta Biomedica Scientifica. 2014;(2):29–31. EDN: SIZJHH
- Ershova OA, Bairova TA. Polymorphism -262C/T of catalase gene (rs1001179) in Russian and Buryat populations with essential hypertension living in the Eastern Siberia. Acta Biomedica Scientifica. 2015;(3):70–73. EDN: UFEBVD
- Golovanova NE, Astratenkova IV, Lukyanova IYu. Gene polymorphism and professional activity as risk factors for the development of arterial hypertension. Vestnik of Saint Petersburg University. Medicine. 2023;18(1):4–11. EDN: DCATWS doi: 10.21638/spbu11.2023.101