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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
[Inflammatory markers of atherosclerotic plaque stabilization after acute coronary event--temporal trends]
Osana Maria Coelho Costa Mouco1, José Carlos Nicolau, Tatiana da Rocha E Souza
1Hospital de Base da Faculdade, Instituto do Coração do Hospital das Clínicas, Faculdade de Medicina de São José do Rio Preto, FMUSP. ocoelho@cardiol.br
Insights
Atherosclerotic plaque stabilization in acute coronary syndromes (ACS) may occur within three months, indicated by inflammatory markers like C-reactive protein (CRP) and factor VIIIc. Interleukin-6 (IL-6) also suggests stabilization by three months and predicts future cardiovascular events.
Area of Science:
- Cardiovascular Medicine
- Inflammation Biology
- Biomarker Research
Context:
- Acute coronary syndromes (ACS) involve plaque instability.
- Understanding plaque stabilization is crucial for managing ACS.
- Inflammatory markers are implicated in ACS pathogenesis.
Purpose:
- To determine the timeline of atherosclerotic plaque stabilization in non-ST-segment elevation ACS (NSTE-ACS).
- To evaluate the utility of inflammatory markers (CRP, fibrinogen, factor VIIIc, IL-6, TNF-alpha) in assessing plaque stabilization.
- To identify inflammatory markers with prognostic value for future cardiovascular events.
Summary:
- In NSTE-ACS patients, C-reactive protein (CRP) and factor VIIIc levels normalized by three months post-discharge, suggesting plaque stabilization.
- Interleukin-6 (IL-6) levels decreased significantly between discharge and three months, indicating stabilization, but remained elevated for six months.
- Only IL-6 demonstrated a significant independent correlation with future cardiovascular events within a year.
Impact:
- Suggests plaque stabilization in ACS patients can be assessed within three months using specific inflammatory markers.
- Highlights IL-6 as a key prognostic biomarker for cardiovascular events post-ACS.
- Provides insights into the temporal dynamics of inflammation and plaque stability after ACS.
Objective:
To evaluate the length of time required for atherosclerotic plaque stabilization in acute coronary syndromes (ACS), using inflammatory markers.
Methods:
In this prospective study, C-reactive protein (CRP), fibrinogen, factor VIIIc, interleukin-6 (IL-6), and tumor necrosis factor-alpha (TNF-alpha) levels were measured on admission, at discharge, and three and six months post-discharge in 40 patients with non-ST-segment elevation ACS (NSTE-ACS) and 40 healthy subjects.
Results:
C-reactive protein levels were significantly higher on admission and at discharge, but not at three and six months post-discharge, compared with the control group. Fibrinogen levels remained unchanged, except at six months, when they were significantly lower than in the control group. Factor VIII-c did not differ from that of the control group on admission, but it was significantly higher at discharge, with no differences at three and six months. Interleukin-6 levels were significantly higher than in the control group in all time points. However, they declined significantly between discharge and three months. In no time point was TNF-alpha significantly different from that of the control group. Only IL-6 correlated significantly and independently with future cardiovascular events.
Conclusion:
With respect to CRP and factor VIIIc, plaque stabilization is suggested in up to three months; IL-6 analysis suggests stabilization as from the third month, although it remained higher than that of the control group for up to six months. Only IL-6 showed prognostic value for further events within a year.
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