The association of RS34643859 gene KCNS1, RS12804550 gene SCN4B, RS4514993 gene SCN11A with the sudden cardiac death


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Introduction. Single nucleotide polymorphisms rs34643859 of the KCNS1 gene, rs12804550 of the SCN4B gene, and rs4514993 of the SCN11A gene were revealed in the analysis of the results of whole exome sequencing of a group of young man died by sudden cardiac death (SCD). The aim of the study is to verify single nucleotide polymorphisms rs34643859, rs12804550, rs4514993 as SCD markers in a case-control study using routine molecular genetic methods and investigate the association with SCD of single nucleotide polymorphisms rs34643859, rs12804550, rs4514993. Methods. SCD group (n=400, average age of the deceased cases acoounted for 53.2+8.7 years, the proportion of men - 70.9%, women - 29.1%) was formed using the SCD criteria of the European Society of Cardiology from the anonymous DNA bank of the deceased sudden death (1999-2019). The control group (n=400, mean age - 53.1+8.3 years, men - 68.3%, women - 31.7%) was matched by sex and age to the SCD group from DNA banks of international projects MONICA and HAPIEE of living at the time of researches participants. Genotyping was carried out using the polymerase chain reaction followed by analysis of restriction fragment length polymorphism. Results. There were no statistically significant differences in the frequencies of genotypes and alleles of single nucleotide polymorphisms rs12804550, rs4514993 between the SCD group and the control group (p>0.05). In the group of women under the age of 50 years, there was a statistically significant decrease in carriers of the TTgenotype rs34643859 in the SCD group (32.3%) compared with the control group (60.0%) (TTvs TC + CC: 0R=0.32, 95% CI: 0.11-0.91, p=0.04). Conclusion. The association of single nucleotide polymorphisms rs12804550 of the SCN4B gene, rs4514993 of the SCN11A gene with SCD has not been confirmed. Single nucleotide polymorphism rs34643859 of the KCNS1 gene is associated with SCD: for women under 50 years of age, the TT polymorphism genotype is associated with a protective effect against SCD.

Full Text

Restricted Access

About the authors

Anastasia Andreevna Ivanova

Research Institutе of Internal and Preventive Medicine - Branch of the Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences

Email: ivanova_a_a@mail.ru
Senior Researcher, Laboratory of Molecular Genetic Research of Therapeutic Diseases

Elizaveta Sergeevna Melnikova

Research Institutе of Internal and Preventive Medicine - Branch of the Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences

Email: jarinaleksi@mail.ru
postgraduate student

Anna Aleksandrovna Gurazheva

Research Institutе of Internal and Preventive Medicine - Branch of the Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences

Email: annapalna1@mail.ru
Junior Researcher, Laboratory of Molecular Genetic Research of Therapeutic Diseases

Sofya Konstantinovna Malutina

Research Institutе of Internal and Preventive Medicine - Branch of the Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences; Novosibirsk State Medical University

Email: smalyutina@hotmail.com
Professor of the Department of Therapy, Hematology and Transfusiology, Faculty of Advanced Training and Professional Retraining of Physicians

Irina Aleksandrovna Rodina

Novosibirsk Regional Office of Forensic Medical Examination

Email: nokbsme@nso.ru
medical forensic expert

Olesya Viktorovna Khamovich

Novosibirsk Regional Office of Forensic Medical Examination

Email: nokbsme@nso.ru
medical forensic expert

Vladimir Pavlovich Novoselov

Novosibirsk State Medical University; Novosibirsk Regional Office of Forensic Medical Examination

Email: nokbsme@nso.ru
Head

Vladimir Nikolaevich Maksimov

Research Institutе of Internal and Preventive Medicine - Branch of the Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences; Novosibirsk State Medical University

Email: medik11@mail.ru
Head of the Laboratory of Molecular Genetic Research of Therapeutic Diseases; Professor of the Department of Medical Genetics and Biology of the Faculty of Medicine and Prevention

References

  1. Шляхто Е.В., Арутюнов Г.П., Беленков Ю.Н. Национальные Рекомендации по определению риска и профилактике внезапной сердечной смерти. Aрхив внутренней медицины. 2013; 4: 5-15.
  2. Priori S.G., Blomstrem-Lundqvist C., Mazzanti A., Blom N., Borggrefe M., Camm J., Elliott P.M., Fitzsimons D., Hatala R., Hindricks G., Kirchhof P., Kjeldsen K., Kuck K.H., Hernandez-Madrid A., Nikolaou N., Norekval T.M., Spaulding C., Van Veldhuisen D.J. The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC). G. Ital Cardiol. 2016; 17 (2):108-70.
  3. dbSNP [Internet]. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information. rs34643859; [released 2020 Apr 21; cited 2020 Oct 18]; Available from: https://www.ncbi.nlm.nih.gov/snp/rs34643859
  4. Hendry L., Lombard Z., Wadley A., Kamer-man P. KCNS1, but not GCH1, is associated with pain intensity in a black southern African population with HIV-associated sensory neuropathy: a genetic association study. J. Acquir Immune Defic Syndr. 2013; 63 (1): 27-30. DOI: 10.1097/ QAI.0b013e318285cf36.
  5. dbSNP [Internet]. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information. rs12804550; [released 2020 Apr 21; cited 2020 Oct 18]; Available from: https://www.ncbi.nlm.nih.gov/snp/rs12804550
  6. Yang Q., Xiong H., Xu C., Huang Y., Tu X., Wu G., Fu F., Wang Z., Wang L., Zhao Y., Li S., Huang Y., Wang C., Wang D., Yao Y., Wang F., Wang Y., Xue Y., Wang P., Chen Q., Pu J., Wang Q.K. Identification of rare variants in cardiac sodium channel p4-subunit gene SCN4B associated with ventricular tachycardia. Mol Genet Genomics. 2019; 294 (4): 1059-71. doi: 10.1007/s00438-019- 01567-7.
  7. Li R.G., Wang Q., Xu Y.J., Zhang M., Qu X.K., Liu X., Fang W.Y., Yang Y.Q. Mutations of the SCN4B-encoded sodium channel p4 subunit in familial atrial fibrillation. Int J. Mol. Med. 2013; 32 (1): 144-50. DOI: 10.3892/ ijmm.2013.1355.
  8. dbSNP [Internet]. Bethesda (MD): National Library of Medicine (US), National Center for Biotechnology Information. rs4514993; [released 2020 Apr 21; cited 2020 Oct 18]; Available from: https://www.ncbi.nlm.nih.gov/snp/rs4514993
  9. Ginanneschi F., Rubegni A., Moro F., Volpi N., Santorelli F.M., Rossi A. SCN11A variant as possible pain generator in sensory axonal neuropathy. Neurol Sci. 2019; 40 (6): 1295-7. doi: 10.1007/s10072-019-3703-4.
  10. Coll M., Allegue C., Partemi S., Mates J., Del Olmo B., Campuzano O., Pascali V., Iglesias A., Striano P., Oliva A., Brugada R. Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing. Int J. Legal Med. 2016; 130 (2): 331-9. doi: 10.1007/s00414-015-1269-0.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2021 Russkiy Vrach Publishing House

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies