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Cytomegalovirus in Plasma of Acute Coronary Syndrome Patients

The relationship between acute coronary syndrome (ACS) and local and systemic inflammation, including accumulation of macrophages in atherosclerotic plaques and upregulation of blood cytokines (e.g., C-reactive protein (CRP)), has been known for more than 100 years. The atherosclerosis-associated in...

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Autores principales: Nikitskaya, E. A., Grivel, J.C., Maryukhnich, E. V., Lebedeva, A. M., Ivanova, O. I., Savvinova, P. P., Shpektor, A. V., Margolis, L. B., Vasilieva, E. Yu.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: A.I. Gordeyev 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947993/
https://www.ncbi.nlm.nih.gov/pubmed/27437144
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author Nikitskaya, E. A.
Grivel, J.C.
Maryukhnich, E. V.
Lebedeva, A. M.
Ivanova, O. I.
Savvinova, P. P.
Shpektor, A. V.
Margolis, L. B.
Vasilieva, E. Yu.
author_facet Nikitskaya, E. A.
Grivel, J.C.
Maryukhnich, E. V.
Lebedeva, A. M.
Ivanova, O. I.
Savvinova, P. P.
Shpektor, A. V.
Margolis, L. B.
Vasilieva, E. Yu.
author_sort Nikitskaya, E. A.
collection PubMed
description The relationship between acute coronary syndrome (ACS) and local and systemic inflammation, including accumulation of macrophages in atherosclerotic plaques and upregulation of blood cytokines (e.g., C-reactive protein (CRP)), has been known for more than 100 years. The atherosclerosis-associated inflammatory response has been traditionally considered as an immune system reaction to low-density lipoproteins. At the same time, some data have indicated a potential involvement of cytomegalovirus (CMV) in the activation and progression of atherosclerosis-associated inflammation, leading to ACS. However, these data have been tangential and mainly concerned the relationship between a coronary artery disease (CAD) prognosis and the anti-CMV antibody titer. We assumed that ACS might be associated with CMV reactivation and virus release into the bloodstream. The study’s aim was to test this assumption through a comparison of the plasma CMV DNA level in patients with various CAD forms and in healthy subjects. To our knowledge, no similar research has been undertaken yet. A total of 150 subjects (97 CAD patients and 53 healthy subjects) were examined. Real- time polymerase chain reaction (RT-PCR) was used to determine the number of plasma CMV DNA copies. We demonstrated that the number of plasma CMV genome copies in ACS patients was significantly higher than that in healthy subjects (p = 0.01). The CMV genome copy number was correlated with the plasma CRP level (p = 0.002). These findings indicate a potential relationship between CMV activation and atherosclerosis exacerbation that, in turn, leads to the development of unstable angina and acute myocardial infarction. Monitoring of the CMV plasma level in CAD patients may be helpful in the development of new therapeutic approaches to coronary atherosclerosis treatment.
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spelling pubmed-49479932016-07-19 Cytomegalovirus in Plasma of Acute Coronary Syndrome Patients Nikitskaya, E. A. Grivel, J.C. Maryukhnich, E. V. Lebedeva, A. M. Ivanova, O. I. Savvinova, P. P. Shpektor, A. V. Margolis, L. B. Vasilieva, E. Yu. Acta Naturae Research Article The relationship between acute coronary syndrome (ACS) and local and systemic inflammation, including accumulation of macrophages in atherosclerotic plaques and upregulation of blood cytokines (e.g., C-reactive protein (CRP)), has been known for more than 100 years. The atherosclerosis-associated inflammatory response has been traditionally considered as an immune system reaction to low-density lipoproteins. At the same time, some data have indicated a potential involvement of cytomegalovirus (CMV) in the activation and progression of atherosclerosis-associated inflammation, leading to ACS. However, these data have been tangential and mainly concerned the relationship between a coronary artery disease (CAD) prognosis and the anti-CMV antibody titer. We assumed that ACS might be associated with CMV reactivation and virus release into the bloodstream. The study’s aim was to test this assumption through a comparison of the plasma CMV DNA level in patients with various CAD forms and in healthy subjects. To our knowledge, no similar research has been undertaken yet. A total of 150 subjects (97 CAD patients and 53 healthy subjects) were examined. Real- time polymerase chain reaction (RT-PCR) was used to determine the number of plasma CMV DNA copies. We demonstrated that the number of plasma CMV genome copies in ACS patients was significantly higher than that in healthy subjects (p = 0.01). The CMV genome copy number was correlated with the plasma CRP level (p = 0.002). These findings indicate a potential relationship between CMV activation and atherosclerosis exacerbation that, in turn, leads to the development of unstable angina and acute myocardial infarction. Monitoring of the CMV plasma level in CAD patients may be helpful in the development of new therapeutic approaches to coronary atherosclerosis treatment. A.I. Gordeyev 2016 /pmc/articles/PMC4947993/ /pubmed/27437144 Text en Copyright ® 2016 Park-media Ltd. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nikitskaya, E. A.
Grivel, J.C.
Maryukhnich, E. V.
Lebedeva, A. M.
Ivanova, O. I.
Savvinova, P. P.
Shpektor, A. V.
Margolis, L. B.
Vasilieva, E. Yu.
Cytomegalovirus in Plasma of Acute Coronary Syndrome Patients
title Cytomegalovirus in Plasma of Acute Coronary Syndrome Patients
title_full Cytomegalovirus in Plasma of Acute Coronary Syndrome Patients
title_fullStr Cytomegalovirus in Plasma of Acute Coronary Syndrome Patients
title_full_unstemmed Cytomegalovirus in Plasma of Acute Coronary Syndrome Patients
title_short Cytomegalovirus in Plasma of Acute Coronary Syndrome Patients
title_sort cytomegalovirus in plasma of acute coronary syndrome patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947993/
https://www.ncbi.nlm.nih.gov/pubmed/27437144
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