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1.
Kardiologiia ; 62(7): 24-30, 2022 Jul 31.
Artigo em Russo, Inglês | MEDLINE | ID: mdl-35989626

RESUMO

Aim      To study the relationship between monomeric C-reactive protein (mCRP) and the progression of asymptomatic carotid atherosclerosis in patients with a moderate risk for cardiovascular diseases (CVD) as assessed with the SCORE model.Material and methods  The study included 80 men and women aged 53.1±5.8 years assigned to the category of a moderate risk for CVDs by the SCORE model with a low-density lipoprotein cholesterol (LDL-C) level of 2.7-4.8 mmol/l and asymptomatic, hemodynamically insignificant (<50% luminal narrowing) carotid atherosclerosis according to ultrasonic data. All patients were prescribed atorvastatin to achieve a LDL-C level <2.6 mmol/l. After 7 years of follow-up, ultrasonic examination of carotid arteries was performed, and concentrations of high-sensitivity C-reactive protein (hsCRP) and mCRP were measured.Results A concentration of LDL-C <2.6 mmol/l was achieved in all patients. The progression of atherosclerosis as determined by an increased number of atherosclerotic plaques (ASPs), was observed in 45 (56 %) patients. At 7 months of follow-up, concentrations of cCRP were higher in the group of patients with progressive carotid atherosclerosis, while the levels of hsCRP did not differ between the groups. Increased mCRP concentrations were associated with changes in variables of the "atherosclerotic load", including the number of ASPs, total ASP height, and the intima-media thickness (IMT). In patients with a median mCRP concentration of 5.2 [3.3; 7.1] µg/l and more, the increases in mean ACP number and total ASP height were considerably higher than in patients with mCRP concentrations lower than the median (3.9 and 2.7 times, respectively), whereas the odds ratio for the progression of asymptomatic carotid atherosclerosis was 5.5 (95 % confidence interval, CI: 2.1-14.6; p=0.001). ROC analysis showed that the concentration of hsCRP had no predictive value for prognosis of asymptomatic carotid atherosclerosis (p=0.16), while the area under the ROC curve (AUC) for mCRP was 0.75±0.056 (95 % CI: 0.64-0.86; p=0.001).Conclusion      According to the results of 7-year follow-up, the plasma concentration of mCRP was significantly higher in patients with an increased number of ASPs than in patients without this increase. An increased level of mCRP may indicate a higher inflammatory risk of CVD.


Assuntos
Aterosclerose , Proteína C-Reativa , Doenças Cardiovasculares , Doenças das Artérias Carótidas , Aterosclerose/sangue , Aterosclerose/diagnóstico , Aterosclerose/metabolismo , Biomarcadores , Proteína C-Reativa/análise , Proteína C-Reativa/metabolismo , Doenças Cardiovasculares/sangue , Doenças Cardiovasculares/metabolismo , Doenças das Artérias Carótidas/sangue , Doenças das Artérias Carótidas/diagnóstico , Doenças das Artérias Carótidas/diagnóstico por imagem , Doenças das Artérias Carótidas/metabolismo , Espessura Intima-Media Carotídea , LDL-Colesterol , Feminino , Fatores de Risco de Doenças Cardíacas , Humanos , Inflamação/metabolismo , Masculino , Pessoa de Meia-Idade , Fatores de Risco
2.
Klin Lab Diagn ; 63(4): 233-238, 2018.
Artigo em Russo | MEDLINE | ID: mdl-30677279

RESUMO

The purpose of study is to investigate significance of detection of number of CD45-positive thrombocytes and ratio neutrophils/lymphocytes in evaluation of risk of development of re-stenosis after implantation of drug-eluting stents in patients with chronic ischemic heart disease and diabetes mellitus type II. The examination was applied to 126 patients with chronic forms of ischemic heart disease who passed through repeat coronary angiography during first year after implantation of drug-eluting stents. The patients were separated on two groups depending on availability of diabetes mellitus type II. In both groups, the patients passed through comparing of angiography and clinical characteristics. Also, a logistic model was developed prognosticating development of re-stenosis. The re-stenosis developed more often in patients with diabetes mellitus type II (54.5%) than in patients without diabetes mellitus type II (32.4%; p=0.01). The comparative analysis of more than 35 characteristics permitted to establish risk factors of development of re-stenosis with the highest prognosticating capacity among patients with diabetes mellitus type II. These risk factors were CD45-positive thrombocytes and ratio neutrophils/lymphocytes. To prognosticate development of re-stenosis a logistic regression model was developed comprising number of circulating CD45-positive thrombocytes, ratio neutrophils/lymphocytes and availability of diabetes mellitus type II. The model demonstrated high prognosticating value as regards development of re-stenosis: OR = 15.1 (95% CI 4.81-31, p < 0.001). The square under ROC-curve: AUC = 0.83 (95% CI 0,72-0,92; р < 0,001). The increasing of number of circulating CD45-positive thrombocytes and ratio neutrophils/lymphocytes can be considered as a valuable risk factors of development of re-stenosis in case of diabetes mellitus type II.


Assuntos
Plaquetas/citologia , Reestenose Coronária/sangue , Diabetes Mellitus Tipo 2/complicações , Linfócitos/citologia , Isquemia Miocárdica/complicações , Neutrófilos/citologia , Constrição Patológica , Angiografia Coronária , Diabetes Mellitus Tipo 2/sangue , Stents Farmacológicos , Humanos , Antígenos Comuns de Leucócito , Isquemia Miocárdica/sangue , Fatores de Risco , Resultado do Tratamento
3.
Bull Exp Biol Med ; 147(6): 726-9, 2009 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-19902068

RESUMO

The content of marker foxp3 of regulatory T cells and chemokines in atherosclerotic plaques of human coronary arteries was measured by the polymerase chain reaction. In vitro migration of regulatory CD4(+)CD25(+)foxp3(+) cells in the CD4(+) lymphocyte population from healthy donors was studied after treatment with chemokines I-309, IP-10, and SDF-1. mRNA for the factor foxp3 and chemokines SDF-1, I-309, and MIP-1beta were found in the majority of samples from atherosclerotic plaques. SDF-1 induced maximum migratory response of CD4(+)CD25(+)foxp3(+) cells.


Assuntos
Aterosclerose/imunologia , Antígenos CD4/imunologia , Vasos Coronários/metabolismo , Fatores de Transcrição Forkhead/imunologia , Regulação da Expressão Gênica , Subunidade alfa de Receptor de Interleucina-2/imunologia , Linfócitos T Reguladores/imunologia , Aterosclerose/metabolismo , Movimento Celular/efeitos dos fármacos , Células Cultivadas , Quimiocina CCL1/metabolismo , Quimiocina CCL4/metabolismo , Quimiocina CXCL10/metabolismo , Quimiocina CXCL12/metabolismo , Fatores de Transcrição Forkhead/metabolismo , Humanos , Reação em Cadeia da Polimerase , Linfócitos T Reguladores/citologia
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