1. Polymorphism of TNF gene in acute coronary syndrome patients: data from the registries ORACLE I and ORACLE II
- Author
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V. A. Brazhnik, L. О. Minushkina, A. О. Averkova, Е. A. Zubova, A. A. Rogozhina, М. A. Evdokimova, A. S. Galyavich, S. N. Tereshchenko, N. A. Koziolova, М. G. Glezer, А. V. Jagoda, О. I. Boeva, Е. V. Khoroletz, Е. А. Karmanchikova, V. O. Konstantinov, G. I. Speshilov, Е. N. Dankovtseva, and D. А. Zateishchikov
- Subjects
tumor necrosis factor ,gene ,acute coronary syndrome ,Diseases of the circulatory (Cardiovascular) system ,RC666-701 - Abstract
Aim. To analyze possible association of the risk of adverse outcomes development in patients post acute coronary episode (ACS), with the polymorphism of gene TNF. Material and methods. To the study, patients included, that were under observation in 2 registry studies ORACLE I and II (Exacerbation of coronary heart disease: logic-probability ways of course prediction and treatment optimization). In overall, 2012 ACS patients assessed. Mean age 64,7±12,69 y.o. There were 1205 males (59,8%) and 807 females (40,2%). 741 patients (36,8%) included with ST elevation ACS, 1271 (63,2%) — with non-ST elevation ACS. Follow-up started at the 10th day from clinical stabilization. Clinical outcomes were gathered based on phone calls with the patients and their relatives, as during the outpatient office visits. Assessment of polymorphisms of gene TNF done with PCR.Results. In the assessed group, the frequency of alleles and gene TNF genotypes were measured: 18 patients carried genotype АА (0,9%), 561 patients — AG (279%), 1433 — GG (71,2%). In those with the allele А gene TNF, more commonly the episodes of SCD were noted (9,8% comparing to 6,6% of GG carriers, p
- Published
- 2018
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