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АSSOCIATION OF VARIOUS GENETIC MARKERS OF CARDIOVASCULAR DISEASES AND SUDDEN CARDIAC DEATH IN MEN

https://doi.org/10.15829/1560-4071-2014-10-40-45

Abstract

Aim. To search and study the association of some candidate genes polymorphysms of various cardiovascular diseases and sudden cardiac death in men.
Material and methods. The sudden cardiac death group (SCD) is collected by the WHO criteria with suddenly died men underwent court-medicine expertise (n=274). Control group was matched by the age and gender from the DNA bank of HAPIEE and MONICA trials. Genotyping of groups was done according to polymorhysms SCN5A, rs187238 gene IL-18, rs1799864 gene CCR2, rs3864180 gene GPC5, rs1799983 gene eNOS, rs2228314 gene SREBF-2, rs1800588 gene HL, rs10757278, rs1333049 with methods of PDRF and realtime PCR.
Results. No significant differences found between the SCD group and control group by the prevalence of genotypes SCN5A, rs187238 gene IL-18, rs3864180 gene GPC5, rs1799983 gene eNOS, rs1800588 gene HL.
In SCD group the decrease of homozygotes by CC polymorphism rs2228314 found in gene SREBF-2 and the decrease of heterozygotes GC comparing to control group (HR=4,074, 95% CI 1,843-9,002, р=0,0002; HR=0,442, 95% CI 0,302-0,647, р=0,0001, reap.). In SCD group carriers of GG genotype polymorphism rs10757278 and CC poly morphism rs1333049 are significantly more prevalent than in control group (HR=1,814, 95% CI 1,159-2,839, р=0,011; HR=1,744, 95% CI 1,104-2,754, р=0,019, resp.). The part of GA carriers of polymorphism rs1799864 gene CCR2 is more prevalent in SCD group comparing to control (HR=1,558, 95% CI 1,051-2,308, р=0,029).
Conclusion. Polymorphisms rs10757278, rs1333049, rs2228314 gene SREBF-2, rs1799864 gene CCR2 are associated with sudden cardiac death in men.

About the Authors

A. A. Ivanova
Scientific-Research Institute for Therapy and Prevention of the SD RAMS, Novosibirsk
Russian Federation


V. N. Maksimov
Scientific-Research Institute for Therapy and Prevention of the SD RAMS; Novosibirsk State Medical University of MH RF, Novosibirsk
Russian Federation


P. S. Orlov
Scientific-Research Institute for Therapy and Prevention of the SD RAMS; Affiliation of the RAS the Institute for Cytology and Genetics of SD RAMS, Novosibirsk
Russian Federation


D. E. Ivanoschuk
Scientific-Research Institute for Therapy and Prevention of the SD RAMS; Affiliation of the RAS the Institute for Cytology and Genetics of SD RAMS, Novosibirsk
Russian Federation


S. V. Savchenko
Novosibirsk State Medical University of MH RF; SHI Novosibirsk Region Bureau of Court-Medicine Expertise, Novosibirsk
Russian Federation


M. I. Voevoda
Scientific-Research Institute for Therapy and Prevention of the SD RAMS; Affiliation of the RAS the Institute for Cytology and Genetics of SD RAMS, Novosibirsk
Russian Federation


References

1. Fan YM, Karhunen P, Levula M, et al. Expression of sterol regulatory element-binding transcription factor (SREBF) 2 and SREBF cleavage-activating protein (SCAP) in human atheroma and the association of their allelic variants with sudden cardiac death. Thrombosis Journal 2008; 6 (17): 1-8.

2. Ayyappa KA, Ghosh S, Mohan V, et al. Association of hepatic lipase gene polymorphisms with hypertriglyceridemia and low high-density lipoprotein-cholesterol levels among South Indian subjects without diabetes. Diabetes Technol Ther. 2013; 15 (6): 503-12.

3. Todur SP, Ashavaid TF. Association of CETP and LIPC Gene Polymorphisms with HDL and LDL Sub-fraction Levels in a Group of Indian Subjects: A Cross-Sectional Study. Indian J Clin Biochem. 2013; 28 (2): 116-23.

4. Hernesniemi JA, Karhunen PJ, Oksala N, et al. Interleukin 18 gene promoter polymorphism: a link between hypertension and pre-hospital sudden cardiac death: the Helsinki Sudden Death Study. European Heart Journal 2009; 30: 2939-46.

5. Nyquist PA, Winkler CA, McKenzie LM, et al. Single nucleotide polymorphisms in monocyte chemoattractant protein-1 and its receptor act synergistically to increase the risk of carotid atherosclerosis. Cerebrovasc Dis. 2009; 28(2): 124-30.

6. Ameno K, Ameno S, Kinoshita H, et al. Autopsy and postmortem examination case study on genetic risk factors for cardiac death: polymorphisms of endothelial nitric oxide synthase gene Glu298Asp variant and T-786C mutation, human paraoxonase 1 (PON1) gene and alpha2beta-adrenergic receptor gene. Vojnosanit Pregl. 2006; 63(4): 357-61.

7. Arking DE, Reinier K, Post W, et al. Genome-wide association study identifies GPC5 as a novel genetic locus protective against sudden cardiac arrest. Plos one 2010; 5 (3): 1-7.

8. Helgadottir A, Thorleifsson G, Manolescu A, et al. A common variant on chromosome 9p21 affects the risk of myocardial infarction. Science 2007; 316 (5830): 1491-3.

9. Bhanushali A, Parmar N, Contractor A, et al. Variant on 9p21 is strongly associated with coronary artery disease but lacks association with myocardial infarction and disease severity in a population in Western India. Arch Med Res 2011; 42 (6): 469-74.

10. George A, Varkony T, Drabkin H, et al. Assignment of the human heart tetrodotoxin- resistant voltage-gated Na(+) channel alpha-subunit gene (SCN5A) to band 3p21. Cytogenet. Cell Genet 1995; 68: 67-70.

11. Chen L, Ballew J, Herron K, et al. A Common polymorphism in SCN5A is associated with lone atrial fibrillation. Clin Pharmacol Ther 2007; 81(1): 35-41.

12. Chen Z, Ding Z, Ma G, et al. Sterol regulatory element-binding transcription factor (SREBF)-2, SREBF cleavage-activating protein (SCAP), and premature coronary artery disease in a Chinese population. Mol Biol Rep 2011; 38: 1-8.

13. Bressler J, Folsom AR, Couper DJ, et al. Genetic variants identified in a European genome- wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study. American Journal of Epidemiology 2009; 171 (1): 14-23.

14. Virani SS, Brautbar A, Lee VV, et al. Chromosome 9p21 single nucleotide polymorphisms are not associated with recurrent myocardial infarction in patients with established coronary artery disease. Circulation Journal 2012; 76: 950-6.

15. Shiffman D, Ellis SG, Rowland CM, et al. Identification of four gene variants associated with myocardial infarction. Am. J. Hum. Genet 2005; 77: 596-605.


Review

For citations:


Ivanova A.A., Maksimov V.N., Orlov P.S., Ivanoschuk D.E., Savchenko S.V., Voevoda M.I. АSSOCIATION OF VARIOUS GENETIC MARKERS OF CARDIOVASCULAR DISEASES AND SUDDEN CARDIAC DEATH IN MEN. Russian Journal of Cardiology. 2014;(10):40-45. (In Russ.) https://doi.org/10.15829/1560-4071-2014-10-40-45

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ISSN 1560-4071 (Print)
ISSN 2618-7620 (Online)