Preview

Eurasian heart journal

Advanced search

INTERETHNIC ASSOCIATIONS OF INCREASED HEART RATE AS A FACTOR OF CARDIOVASCULAR RISK. PART 2: GENETIC MARKERS

https://doi.org/10.38109/2225-1685-2021-1-88-93

Abstract

Purpose. To study the genetic aspects of increased heart rate (HR) in representatives of various ethnic groups living in Mountain Shoria.
Material and Methods. The study involved residents of the villages of Mountain Shoria aged 18 years and older. Included are 901 people – representatives of indigenous nationality (Shors), 408 people – of nonindigenous nationality. The groups did not differ by gender and age. The analysis was carried out depending on the increased level of heart rate (over 80 beats/min). Typing of polymorphic sites of the ACE (I/D, rs4340), ADRB1 (p.145A> G, Ser49Gly, rs1801252), ADRA2B (I/D, rs28365031), MTHFR (c.677C> T, Ala222Val, rs1801133) and NOS3 (VNTR, 4b/4a) was carried out using polymerase chain reaction. The association of different genotypes with heart rates above 80 beats/min was judged by the odds ratio in five inheritance models (codominant, dominant, recessive, overdominant and log-additive), and its 95% confidence interval was calculated.
Results. Ethnic features of the prevalence of increased heart rate have been established depending on the polymorphism of candidate genes involved in the pathogenesis of arterial hypertension. The respondents of the indigenous ethnic group had a high probability of developing tachycardia determined by the carriage of the C/T genotype of the MTHFR gene according to an overdominant type of inheritance [OR = 2.46]. Allele D of the ACE gene determined the tendency to the development of this pathology according to the recessive type of inheritance [OR = 1.91]. However, among young people and men, carriage of a prognostically unfavorable D/D genotype of this gene was associated with a high risk of increased heart rate [OR = 3.34] and [OR = 4.62], respectively. In a cohort of non-indigenous nationality, the heterozygous genotype I/D of the ACE gene determined the likelihood of tachycardia by an overdominant type of inheritance [OR = 2.08].
Conclusions. Most epidemiological studies show a significant difference in the contribution of the studied polymorphisms to the appearance of increased heart rate for various ethnic groups. For a small population of Mountain Shoria, genetic features of the development of tachycardia have been established. In this regard, it is advisable to take into account national characteristics when determining individual risk, and apply personalization to correction programs.

About the Authors

T. A. Mulerova
Federal State Budgetary Institution Research Institute for Complex Issues of Cardiovascular Diseases
Russian Federation

Dr. of Sci. (Med.), Researcher at the laboratory of cardiovascular disease epidemiology

Kemerovo, 650002



M. Yu. Ogarkov
Federal State Budgetary Institution Research Institute for Complex Issues of Cardiovascular Diseases
Russian Federation

Dr. of Sci. (Med.), Professor, Researcher at the laboratory of cardiovascular disease epidemiology

Kemerovo, 650002



References

1. Shalnova S.A., Deev A.D., Belova O.A. et al. on behalf of the participants of the ESSE-RF study. Heart rate and its association with the main risk factors in the population of men and women of working age. Rational pharmacotherapy in cardiology. 2017; 13(6):819–826 (In Russ.) Doi: 10.20996/1819-6446-2017-13-6-819-826

2. Dudchenko I.A., Pristupa L.N., Ataman A.V., Garbuzova V.Yu. Genetic dependency of blood pressure and heart rate in patients with arterial hypertension and obesity. Annals of the Russian Academy of Medical Sciences. 2014; 5-6: 40–46 (In Russ.)

3. Ponasenko A.V., Tsepokina A.V., Tkhorenko B.A. et al. Variability of mitochondrial DNA in the development of atherosclerosis and myocardial infarction (a review). Complex Issues of Cardiovascular Diseases. 2018; 7(4S): 75–85 (In Russ.) https://doi.org/10.17802/2306-1278-2018-7-4S-75-85.

4. Fomchenko N.E., Voropaev E.V., Salivonchik S.P. Molecular and genetic aspects in studying of cardiovascular patology. Health and environmental issues. 2009; 2(20): 42–48 (In Russ.)

5. Chazova I.E., ZhernakovaYu.V. on behalf of the experts. Clinical guidelines. Diagnosis and treatment of arterial hypertension. Systemic Hypertension. 2019; 16(1): 6–31 (In Russ.) Doi: 10.26442/2075082X.2019.1.190179

6. Barbarash О.L., Voevoda М.I., Artamonova G.V. et al. Genetic determinants of hypertension in two national cohorts of Mountain Shoria. Therapeutic Archive. 2017; 89(9):68–77 (In Russ.) Doi: 10.17116/terarkh201789968-77

7. Mulerova T.A., Ponasenko A.V., Tsepokina A.V. et al. Аssociations of angiotensinogen gene polymorphism (AGT, rs699) with arterial hypertension and its risk factors in residents of Mountain Shoria. Russian Journal of Cardiology. 2017; 10: 85–92 (In Russ.) Doi: 10.15829/1560-4071-2017-10-85-92

8. Timasheva Ya.R., Nasibullin T.R., Imaeva E.B. et al. Beta-adrenoreceptor gene polymorphisms and the risk of essential hypertension. Arterial Hypertension. 2015; 21(3): 259–266 (In Russ.) Doi: 10.18705/1607-419X-2015-21-3-259-266.

9. Ueberham L., Bollmann A., Shoemaker M.B. et al. Genetic ACE I/D polymorphism and recurrence of atrial fibrillation after catheter ablation. Circ Arrhythm Electrophysiol. 2013; 6(4): 732–737. http://doi.org/10.1161/CIRCEP.113.000253.

10. Feng W., Sun L., Qu X.F. Association of AGTR1 and ACE2 gene polymorphisms with structural atrial fibrillation in a Chinese Han population. Pharmazie. 2017; 72(1): 17–21. http://doi.org/10.1691/ph.2017.6752.

11. Ma R., Li X., Su G. et al. Angiotensin-converting enzyme insertion/deletion gene polymorphisms associated with risk of atrial fibrillation: A metaanalysis of 23 case-control studies. J Renin Angiotensin Aldosterone Syst. 2015; 16(4): 793–800. http://doi.org/10.1177/1470320315587179.

12. Kolomeichuk S.N., Alekseev R.V., Putilov A.A., Meigal A.Yu. Association of polymorphic variants of ACE and BDKRB2 with heart rate variability in athletes of the republic Karelia. Bulletin of the Russian state medical university.2017; 4: 50–58 (In Russ.)

13. Zhang X., Wang C., Dai H. et al. Association between angiotensinconverting enzyme gene polymorphisms and exercise performance in patients with COPD. Respirology. 2008; 13(5): 683–688.

14. Bickel C., Schnabel R.B., Zengin E. et all. Homocysteine concentration in coronary artery disease: Influence of three common single nucleotide polymorphisms. Nutr Metab Cardiovasc Dis. 2017; 27(2): 168–175. http://doi.org/10.1016/j.numecd.2016.09.005.

15. Yakushin S.S., Solodun M.V. The gene polymorphism of beta1-adrenoreceptor, postinfarction myocardial remodeling and cardiovascular risk: is there any correlation? Medical Council. 2018; 5: 42–46 (In Russ.) Doi: 10.21518/2079-701X-2018-5-42-46

16. Alyavi B.A., Tursunov R.R., Iskhakov Sh.A. et al. Clinical efficacy of bisoprolol in patients with coronary heart disease depending on the type of polymorphic marker of the ADRB-1 gene. Bukovinian Medical Bulletin. 2014; 18(1): 7–11 (In Russ.)

17. White H.L., de Boer R.A., Maqbool A. et al. An evaluation of the beta-1 adrenergic receptor Arg389Gly polymorphism in individuals with heart failure: a MERIT-HF sub-study. Eur. J. Heart Failure. 2003; 5(4): 463–468.

18. Zamakhina O.V., Bunova S.S., Nikolaev N.A., Nelidova A.V. The effect of Arg389Gly and Ser49Gly polymorphisms of the ADRB1 gene on the effectiveness of treatment with bisoprolol in patients with stable angina pectoris who had myocardial infarction. RMG. «Medical Review». 2018; 11: 30–34 (In Russ.)


Review

For citations:


Mulerova T.A., Ogarkov M.Yu. INTERETHNIC ASSOCIATIONS OF INCREASED HEART RATE AS A FACTOR OF CARDIOVASCULAR RISK. PART 2: GENETIC MARKERS. Eurasian heart journal. 2021;(1):88-93. (In Russ.) https://doi.org/10.38109/2225-1685-2021-1-88-93

Views: 399


ISSN 2225-1685 (Print)
ISSN 2305-0748 (Online)