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qPCR Is a Sensitive and Rapid Method for Detection of Cytomegaloviral DNA in Formalin-fixed, Paraffin-embedded Biopsy Tissue
Published on: July 9, 2014
Cytomegalovirus in Plasma of Acute Coronary Syndrome Patients
E A Nikitskaya1, J C Grivel2, E V Maryukhnich1
1Laboratory of Atherothrombosis, Cardiology Department, Evdokimov Moscow State University of Medicine and Dentistry, Delegatskaya str. 20/1, 127473, Moscow, Russia;
Insights
Cytomegalovirus (CMV) reactivation may drive acute coronary syndrome (ACS) by exacerbating atherosclerosis. Higher CMV DNA levels in ACS patients suggest a link between CMV activation and cardiovascular events.
Area of Science:
- Cardiology
- Infectious Diseases
- Immunology
Background:
- The link between inflammation and acute coronary syndrome (ACS) is well-established, involving macrophages and cytokines like C-reactive protein (CRP).
- Cytomegalovirus (CMV) has been tentatively associated with atherosclerosis progression, but direct evidence linking CMV reactivation to ACS is limited.
Purpose of the Study:
- To investigate the association between cytomegalovirus (CMV) reactivation and acute coronary syndrome (ACS).
- To compare plasma CMV DNA levels in patients with coronary artery disease (CAD) and healthy individuals.
Main Methods:
- Quantitative analysis of plasma CMV DNA using real-time polymerase chain reaction (RT-PCR).
- Inclusion of 150 subjects: 97 with CAD and 53 healthy controls.
Main Results:
- Significantly higher plasma CMV DNA levels were observed in ACS patients compared to healthy subjects (p = 0.01).
- CMV genome copy number positively correlated with plasma C-reactive protein (CRP) levels (p = 0.002).
Conclusions:
- CMV activation may play a role in the exacerbation of atherosclerosis, contributing to ACS development.
- Monitoring plasma CMV levels could inform new therapeutic strategies for coronary atherosclerosis.
Abstract:
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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