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We investigated the association of polymorphisms of genes FGB G(-455)A and PROCC(-1654)T with coronary artery disease (CAD) in the Russian population. A total of 1145 patients with CAD diagnose on the basis of clinical studies in cardiological hospitals of Moscow, St. Petersburg, Kazan, Chelyabinsk, Perm, Stavropol and Rostov-on-Don. Supervision term was 1.14 +/- +/- 0.33 years (the maximum term 3.2 years). The group studied do not differ significantly with respect to the distributions of G(-455)A alleles and genotypes. However in case of gene PROC C(-1654)T polymorphism we determined that patients with CAD diagnose and Talleles of PROC gene had unfavorable outcome more often than patients with homozygous C alleles. Survival time from end point from carrier phenotype TT and CTis 2.19 +/- 0.18 r. years against 2.46 +/- 0.16 from carrier phenotype CCgene PROC. The obtained data allows to assume the important role of the genes which are responsible for functioning of system of a hemostasis, in the accelerated formation of failures at the patients who had a coronary syndrome.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrinógeno / Proteína C / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Síndrome Coronario Agudo Tipo de estudio: Clinical_trials Límite: Female / Humans / Male / Middle aged País/Región como asunto: Asia / Europa Idioma: Ru Revista: Mol Biol (Mosk) Año: 2010 Tipo del documento: Article Pais de publicación: Rusia
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibrinógeno / Proteína C / Predisposición Genética a la Enfermedad / Polimorfismo de Nucleótido Simple / Síndrome Coronario Agudo Tipo de estudio: Clinical_trials Límite: Female / Humans / Male / Middle aged País/Región como asunto: Asia / Europa Idioma: Ru Revista: Mol Biol (Mosk) Año: 2010 Tipo del documento: Article Pais de publicación: Rusia