Preview

Russian Journal of Cardiology

Advanced search

FIRST RUSSIA-BASED STUDY OF POLYMORPHISM rs2200733 CHROMOSOME 4q25 ASSOCIATION WITH DEVELOPMENT OF THE LONE ATRIAL FIBRILLATION

https://doi.org/10.15829/1560-4071-2016-10-28-31

Abstract

Atrial fibrillation (AF) is one of the most prevalent tachiarrhythmias, with at date non fully understood etiology. Recently, the attention is paid to genetic determinants of AF.

Aim. To assess the role of rs2200733 polymorhpism on the chromosome 4q25 in development of AF in Russian population.

Material and methods. Totally, 76 patients studied with AF, and control group, number 73 persons without cardiovascular pathology. All participants underwent laboratory and genetic investigations.

Results. A statistically significant prevalence of genotype ТТ is found (21,21% vs 4,11%, р=0,015) and allele Т (34,85% vs 19,86%, р=0,03) in the group of patients with the lone AF comparing to the controls. Therefore, TT genotype and T allele of rs2200733 chromosome 4q25 could be predictors of unknown origin AF development.

About the Authors

V. A. Shulman
V. F. Voino-Yasenetsky Krasnoyarsk State Medical University, Krasnoyarsk
Russian Federation


S. Yu. Nikulina
V. F. Voino-Yasenetsky Krasnoyarsk State Medical University, Krasnoyarsk
Russian Federation


N. V. Aksyutina N
V. F. Voino-Yasenetsky Krasnoyarsk State Medical University, Krasnoyarsk
Russian Federation


E. E. Poplavskaya
V. F. Voino-Yasenetsky Krasnoyarsk State Medical University, Krasnoyarsk
Russian Federation


B. V. Nazarov
V. F. Voino-Yasenetsky Krasnoyarsk State Medical University, Krasnoyarsk


V. N. Maksimov
Scientific-Research Institute of Therapy and Prevention, Novosibirsk, Russia
Russian Federation


References

1. Diagnosis and treatment of atrial fibrillation. Recommendation of RCS, ASSC and ACS. Rus J Cardiol 2013; 4(3) р. 100. Russian (Диагностика и лечение фибрилляции предсердий. Рекомендации РКО, ВНОА и АССХ. Российский кардиологический журнал 2013, 4(3) c. 100).

2. Lloyd-Jones DM, Wang TJ, Leip EP, et al. Lifetime risk for development of atrial fibrillation: the Framingham Heart Study. Circulation 2004; 110(9): 1042-6.

3. Niculina SYu, Sulman VA, Kuznecova OO, et al. Clinical and genetic features of atrial fibrillation. Racional’naja farmakoterapija v kardiologii 2008; 4(2): 13-8. Russian (Никулина С. Ю., Шульман В. А., Кузнецова О. О. и др. Клинико-генетические особенности фибрилляции предсердий. Рациональная фармакотерапия в кардиологии 2008, 4(2): 13- 8).

4. Sulman VA, Niculina SYu, Dudkina KV, et al. The role of the alpha-2-beta-adrenergic receptors gene in the genesis of atrial fibrillation. Sib. med. obozrenie 2010; 62(2): 25-9. Russian (Шульман В. А., Никулина С. Ю., Дудкина К. В. и др. Роль гена альфа-2-бета-адренорецепторов в генезе фибрилляции предсердий. Сибирское медицинское обозрение 2010; 62(2): 25-9).

5. Oslopov VN, Oslopova YuV. 20 years in search of “the gene for atrial fibrillation”. Prakticheskaja medicina 2013; 3: 12-14. Russian (Ослопов В. Н., Ослопова Ю. В. 20 лет в поисках “гена фибрилляции предсердий”. Практическая медицина 2013; 3: 12-14).

6. Erastova EK, Dikevich EP, Shkol’nikova MA. The mechanisms of development and maintenance of atrial flutter and atrial fibrillation in children. Lechashchij vrach 2011; 7. Russian (Ерастова Е. К., Дикевич Е. П., Школьникова М. А. Механизмы развития и поддержания трепетания и фибрилляции предсердий в детском возрасте. Лечащий врач 2011; 7). http://www.lvrach.ru/2011/07/15435239/ (2 September 2011).

7. Tatarskij BA, Batalov RE, Popov SV. Atrial fibrillation: pathophysiological approach to the choice of antiarrhythmic therapy. Tomsk: STT, 2013: 46. Russian (Татарский Б. А., Баталов Р. Е., Попов С. В. Фибрилляция предсердий: патофизиологические подходы к выбору антиаритмической терапии. Томск: STT, 2013: 46.

8. Olesen MS, Holst AG, Jabbari J, et al. Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years. Can J Cardiol 2012; 28(2): 191-5.

9. Gudbjartsson DF, Arnar DO, Helgadottir A, et al. Variants conferring risk of atrial fibrillation on chromosome 4q25. Nature 2007; 448(7151): 353-7.

10. Ferrán A, Alegret JM, Subirana I, et al. Association between rs2200733 and rs7193343 genetic variants and atrial fibrillation in a Spanish population, and meta-analysis of previous studies. Rev Esp Cardiol (Engl Ed) 2014; 67(10): 822-9.

11. Kirchhof P, Bax J, Blomstrom-Lundquist C, et al. Early and comprehensive management of atrial fibrillation: executive summary of the proceedings from the 2nd AFNET-EHRA consensus conference ‘research perspectives in AF. Eur Heart J 2009; 30(24): 2969-77.

12. Page SP, Siddiqui MS. Catheter ablation for atrial fibrillation on uninterrupted warfarin: can it be done without echo guidance? J Cardiovasc Electrophysiol 2011; 22(3): 265-70.

13. Mohanty S, Santangeli P, Bai R, et al. Variant rs2200733 on chromosome 4q25 confers increased risk of atrial fibrillation: evidence from a meta-analysis. J Cardiovasc Electrophysiol 2013; 24(2): 155-61.

14. Kiliszek M, Franaszczyk M, Kozluk E, et al. Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population. PLoS One 2011; 6(7): e21790.

15. Goodloe AH, Herron KJ, Olson TM. Uncovering an intermediate phenotype associated with rs2200733 at 4q25 in lone atrial fibrillation. Am. J. Cardiol. 2011; 107(12): 1802-5.

16. Lubitz SA, Sinner MF, Lunetta KL, et al. Independent susceptibility markers for atrial fibrillation on chromosome 4q25. Circulation 2010; 122(10): 976-84.

17. Viviani Anselmi C, Novelli V, Roncarati R, et al. Association of rs2200733 at 4q25 with atrial flutter/fibrillation diseases in an Italian population. Heart 2008; 94(11): 1394-6.

18. Lee KT, Yeh HY, Tung CP, et al. Association of RS2200733 but not RS10033464 on 4q25 with atrial fibrillation based on the recessive model in a Taiwanese population. Cardiology 2010; 116(3): 151-6.

19. Shi L, Li C, Wang C, et al. Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population. Hum Genet 2009; 126(6): 843-9.


Supplementary files

1. Рисунок1
Subject
Type Исследовательские инструменты
Download (17KB)    
Indexing metadata ▾
2. Рисунок2
Subject
Type Исследовательские инструменты
Download (33KB)    
Indexing metadata ▾
3. Рисунок3
Subject
Type Исследовательские инструменты
Download (16KB)    
Indexing metadata ▾
4. Рисунок4
Subject
Type Исследовательские инструменты
Download (247KB)    
Indexing metadata ▾
5. Рисунок5
Subject
Type Исследовательские инструменты
Download (40KB)    
Indexing metadata ▾
6. Рисунок6
Subject
Type Исследовательские инструменты
Download (203KB)    
Indexing metadata ▾
7. Рисунок7
Subject
Type Исследовательские инструменты
Download (195KB)    
Indexing metadata ▾
8. Рисунок8
Subject
Type Исследовательские инструменты
Download (239KB)    
Indexing metadata ▾
9. Сопроводительное письмо
Subject
Type Исследовательские инструменты
Download (91KB)    
Indexing metadata ▾
10. Конфликт
Subject
Type Исследовательские инструменты
Download (21KB)    
Indexing metadata ▾
11. Этика
Subject
Type Исследовательские инструменты
Download (22KB)    
Indexing metadata ▾
12. Титульный лист
Subject
Type Исследовательские инструменты
Download (14KB)    
Indexing metadata ▾
13. Сопроводительное письмо
Subject
Type Other
Download (91KB)    
Indexing metadata ▾
14. титульный лист
Subject
Type Other
Download (17KB)    
Indexing metadata ▾

Review

For citations:


Shulman V.A., Nikulina S.Yu., Aksyutina N N.V., Poplavskaya E.E., Nazarov B.V., Maksimov V.N. FIRST RUSSIA-BASED STUDY OF POLYMORPHISM rs2200733 CHROMOSOME 4q25 ASSOCIATION WITH DEVELOPMENT OF THE LONE ATRIAL FIBRILLATION. Russian Journal of Cardiology. 2016;(10):28-31. (In Russ.) https://doi.org/10.15829/1560-4071-2016-10-28-31

Views: 793


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


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