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    S.M. Pyvovar, Yu.S. Rudyk, T.V. Lozyk, V.Yu. Galchinska

    POLYMORPHISM OF C825T (RS5443) G-PROTEIN 3-SUBUNIT GENE AND THE LONG-TERM PROGNOSIS FOR PATIENTS WITH HEART FAILURE


    About the author: S.M. Pyvovar, Yu.S. Rudyk, T.V. Lozyk, V.Yu. Galchinska
    Heading CLINICAL MEDICINE
    Type of article Scentific article
    Annotation Forecasting of an unfavorable course in heart failure is very relevant. The purpose of the work was to determine the effect of the G protein β3-subunit C825T (RS5443) gene polymorphism on the long-term prognosis for patients with heart failure. The study included 170 patients with heart failure on the background of post-infarction cardiosclerosis. The G protein β3-subunit C825T (RS5443) gene polymorphism was determined by means of the polymerase chain reaction. Daily monitoring of ECG, Doppler echocardioscopy were carried out. The observation period was 3 years, whereby the course of the disease was evaluated, the atrial fibrillation paroxysms development, the frequency of hospitalizations due to the disease decompensation, and mortality were taken into account. The frequencies of the C825T (RS5443) polymorphic variants of the G protein β3-subunit gene were determined in the patients. 47% of patients are homozygous carriers of C825 alleles, 47% of patients are heterozygotes (C825T), 11 out of 170 patients are homozygous by the T genome. Homozygous patients with T genome are younger by 7.5 years, compared to homozygous C-allele patients and by 6 years younger compared to heterozygotes (CT) (p <0.01). For 3 years, in the patients homozygous by the T-allele, an increase in the left ventricle end-diastolic volume (by 6%, p <0.05) and a decrease in the amount of left ventricular ejection fraction (by 11%, p <0.05) was observed. In 5 out of 11 patients with heart failure who are homozygous by the T allele (TT), in the third year of observation, a pathological number of ventricular extrasystoles is recorded. Among the homozygous by the C-allele (CC) and heterozygous (CT) patients, this type of rhythm disorder is statistically reliably less frequent (χ2 = 6.854; p <0.05). The tendency was revealed towards a higher frequency of hospitalization in patients due to the disease decompensation for 3 years in the group of homozygous patients with T-allele.
    Tags heart failure, clinical course, atrial fibrillation, C825T (RS5443) polymorphism, gene, β3 subunit of G protein
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    Publication of the article «World of Medicine and Biology» №1(67), 2019 year, 088-093 pages, index UDK 616.12-008.44-085.22:576.8.095.52
    DOI 10.26724/2079-8334-2019-1-67-88