Author Affiliations1Institute of Internal Medicine, SB of RAMS 630089, Novosibirsk, Boris Bogatkov str., 175/1
2Novosibirsk State Medical University of Minzdrav of Russia 630091, Novosibirsk, Krasny av., 52
3Novosibirsk State Medical University of Minzdrav of Russia 630091, Novosibirsk, Krasny av., 52
4Institute of Internal and Preventive Medicine of SB RAMS 630089, Novosibirsk, Boris Bogatkov str., 175/1, Institute of Cytology and Genetics of SB RAS 630090, Novosibirsk, Akademic Lavrentev av., 10
5Novosibirsk State Medical University of Minzdrav of Russia 630091, Novosibirsk, Krasny av., 52
6Institute for Internal and Preventive Medicine of SB RAMS 630090, Novosibirsk, Boris Bogatkov str., 175/1
1. Malygina N.A., Kostomarova I.V., Melent'ev A.S. et al. ACE gene I/D-polymorphism and hereditary predisposition to myocardial infarction // Klinicheskaya meditsina. 2002. 80. (8). 25–29. (in Russian)
2 Smith C.L., Klco S.R., Cantor C.R. Pulsed-field gel electrophoresis and the technology of large DNA molecules // Genome Analysis: A Practical Approach. Ed. K. Davies. Oxford: Oxford Univ. Press. 41–72. (in Russian)
3. Aschauer S., Mittermayer F., Wagner C.C. et al. Forearm vasodilator reactivity in homozygous carriers of the 9p21.3 rs1333049 G > C polymorphism // Eur. J. Clin. Invest. 2010. 40. (8). 700–705.
4. Biros E., Cooper M., Palmer L.J. et al. Association of an allele on chromosome 9 and abdominal aortic aneurysm // Atherosclerosis. 2010. 212. (2). 539–542.
5. Deka R., Koller D.L., Lai D. et al. FIA Study Investigators. The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm // Stroke. 2010. 41. (6). 1132–1137.
6. Franceschini N., Carty C., Bůzková P., Reiner A. Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study // Circ. Cardiovasc. Genet. 2011. 4. (6). 661–672.
7. Larson M.G., Atwood L.D., Benjamin E.J. et al. Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes // BMC Med. Genet. 2007. 8. (Suppl. 1). S5.
8. Mendonça I., dos Reis R.P., Pereira A. et al. Independent association of the variant rs1333049 at the 9p21 locus and coronary heart disease // Rev. Port. Cardiol. 2011. 30. (6). 575–591.
9. O’Donnell C.J., Kavousi M., Smith A.V. et al. Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction // Circulation. 2011. 124. (25). 2855–2864.
10. Plichart M., Empana J.P., Lambert J.C. et al. Single polymorphism nucleotide rs1333049 on chromosome 9p21 is associated with carotid plaques but not with common carotid intima-media thickness in older adults. A combined analysis of the Three-City and the EVA studies // Atherosclerosis. 2012. 222. (1). 187–190.
11. Preuss M., König I.R., Thompson J.R. et al. Design of the Coronary ARtery DIsease Genome-Wide Replication And Meta-Analysis (CARDIoGRAM) Study: A Genome-wide association meta-analysis involving more than 22 000 cases and 60 000 controls.CARDIoGRAM Consortium // Circ. Cardiovasc. Genet. 2010. 3. (5). 475–483.
12. Scheffold T., Kullmann S., Huge A. et al. Forschungsverbund Herz-Kreislauf in NRW (Research Consortium Heart and Circulation in North Rhine-Westphalia). Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry // BMC Cardiovasc. Disord. 2011. 11. doi:10.1186/1471-2261-11-9.
13. Schunkert H., Götz A., Braund P. et al. Cardiogenics Consortium. Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease // Circulation. 2008. 117(13). 1675–1684.
14. Tang E.W., Wong C.K., Herbison P. Global Registry of Acute Coronary Events (GRACE) hospital discharge risk score accurately predicts long-term mortality post acute coronary syndrome. // Am. Heart J. 2007. 153. (1). 29–35.
15. The chromosome 9p21 region and myocardial infarction in a European population // Atherosclerosis. 2011. 217. (1). 220–226.
16. Virani S.S., Brautbar A., Lee V.V. et al. Association of genetic variants and incident coronary heart disease in multi-ethnic cohorts. The PAGE Study // Circ. Cardiovasc. Genet. 2011. 4. (6). 661–772.
About Authors (Correspondence):
Kulikov I.V. – candidate of medical sciences, senior researcher of the laboratory of molecular genetic studies of therapeutic diseases, e-mail: 248945@mail.ru
Lozhkina N.G. – candidate of medical sciences, assistant professor of the chair of internal diseases, e-mail: lozhkina.n@mail.ru
Maksimov V.N. – doctor of medical sciences, head of laboratory of molecular genetic studies of therapeutic diseases, e-mail: medik11@mail.ru
Orlov P.S. – junior researcher of the laboratory of molecular basis of animal genetics, e-mail: orlovpavel86@gmail.com
Kuimov A.D. – doctor of medical sciences, professor, head of the chair of internal diseases, e-mail: terapia@mail.ru
Voevoda M.I. – doctor of medical sciences, professor, corresponding member of RAMS, director, e-mail: mvoevoda@ya.ru