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1.
Kardiologiia ; 60(2): 83-88, 2020 Mar 05.
Article in Russian | MEDLINE | ID: mdl-32345203

ABSTRACT

OBJECTIVE: The aim of the study was to study biochemical factors of calcification in stable and unstable plaques of coronary arteries and in the blood of patients with severe coronary atherosclerosis, to find associations of biochemical factors of calcification with the development of unstable atherosclerotic plaque. MATERIALS AND METHODS: The study included 25 men aged 60,4±6,8 years who received coronary bypass surgery. In the course of the operation intraoperative indications in men were from coronary endarteriectomy (s) artery (a - d) and histological and biochemical analyses of the samples of the intima / media. Out of 85 fragments of intima / media of coronary arteries, 15 fragments of unchanged intima / media, 39 fragments of stable atheromatous plaque and 31 fragments of unstable plaque were determined. In homogenates of samples of intima / media (after measurement of protein by the method of Lowry) and in blood by ELISA were determined by biochemical factors of calcification: osteoprotegerin, osteocalcin, an osteopontin, osteonectin, as well as inflammatory factors (cytokines, chemokines). RESULTS: A significant direct correlation (Spearman coefficient =0.607, p<0.01) between the stages of atherosclerotic focus development to unstable plaque and the degree of calcification of atherosclerotic focus development samples was found. There was an increased content of osteocalcin in stable and unstable plaques by 3.3 times in comparison with the unchanged tissue of intima / media of coronary arteries, as well as in samples with small and dust-like, with coarse-grained calcifications in comparison with samples without calcifications by 2.8 and 2.1 times, respectively. According to multivariate logistic regression analysis, the relative risk of unstable atherosclerotic plaque in the coronary artery is associated with a reduced content of osteocalcin (OR=0.988, 95 % CI 0.978-0.999, p=0.028). Also, the relative risk of calcifications in the atherosclerotic plaque in the coronary artery is associated with an increased content of osteocalcin (OR=1,008, 95 % CI 1,001-1,015, p=0,035). In men with severe coronary atherosclerosis, a significant inverse correlation was found (Spearman coefficient -0.386, p=0.022) between the content of osteoprotegerin in the vascular wall and in the blood.


Subject(s)
Atherosclerosis , Calcinosis , Coronary Artery Disease , Plaque, Atherosclerotic , Aged , Carotid Intima-Media Thickness , Coronary Vessels , Humans , Male , Middle Aged , Risk Factors
2.
BMC Res Notes ; 12(1): 336, 2019 Jun 13.
Article in English | MEDLINE | ID: mdl-31196144

ABSTRACT

OBJECTIVE: The study was dedicated to investigation of some hemostasis and endothelial dysfunction factors association with probability of presence of vulnerable atherosclerotic plaques in coronary arteries in men with atherosclerosis. RESULTS: The blood levels of factor VII, factor XII and MCP-1 were higher, and concentration of sVCAM-1 lower in men with vulnerable atherosclerotic plaques in the coronary arteries, compared to men who had stable plaques. Have been revealed correlation links between the blood levels of factor II, factor XII, MCP-1 and the presence of vulnerable atherosclerotic plaques in the coronary arteries. Results of logistic regression analysis showed that the relative risk of present of vulnerable atherosclerotic plaques in the coronary arteries is associated with an elevated blood level of factor XII and MCP-1.


Subject(s)
Atherosclerosis/physiopathology , Coronary Artery Disease/physiopathology , Endothelium, Vascular/physiopathology , Hemostasis , Plaque, Atherosclerotic/physiopathology , Aged , Atherosclerosis/blood , Chemokine CCL2/blood , Coronary Artery Disease/blood , Coronary Vessels/metabolism , Coronary Vessels/physiopathology , Endothelium, Vascular/metabolism , Factor XII/metabolism , Humans , Logistic Models , Male , Middle Aged , Plaque, Atherosclerotic/blood , Probability , Prothrombin/metabolism , Vascular Cell Adhesion Molecule-1/blood
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