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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
[Inflammatory biomarker for diagnosis of coronary diseases]
Hirofumi Soejima1, Hideki Kishikawa, Hisao Ogawa
1Health Care Center, Kumamoto University.
Insights
Biomarkers of inflammation, including adhesion molecules and matrix metalloproteases, are linked to acute coronary syndromes. These markers indicate atherosclerotic plaque development and the risk of coronary events.
Area of Science:
- Cardiology
- Biochemistry
- Immunology
Context:
- Acute coronary syndromes (ACS) result from complex inflammatory processes.
- Plaque rupture, thrombosis, and obstruction are key pathological features of ACS.
- Inflammation plays a central role in the development and progression of atherosclerosis.
Purpose:
- To explore the role of specific inflammatory biomarkers in acute coronary syndromes.
- To investigate the association between blood levels of certain molecules and ACS.
- To evaluate the predictive value of these biomarkers for coronary events.
Summary:
- This review discusses inflammatory biomarkers such as adhesion molecules, matrix metalloproteases (MMPs), monocyte chemoattractant protein-1 (MCP-1), tissue factor, and interferon-gamma (IFN-γ).
- Elevated levels of these biomarkers are associated with the formation and progression of atherosclerotic plaques.
- These markers are also linked to the incidence of coronary events in patients with ACS.
Impact:
- Identifies key inflammatory markers associated with ACS.
- Highlights the link between inflammation, atherosclerosis, and coronary events.
- Provides insights for potential diagnostic and prognostic tools in cardiology.
Abstract:
Acute coronary syndromes are multifactorial and occur in response to inflammation, plaque rupture and subsequent thrombosis, progressive mechanical obstruction, and dynamic obstruction. Among potential biomarkers, much interest has focused on biomarkers of inflammation. The process that leads to eventual plaque erosion or rupture involves a number of inflammatory mechanisms, including endothelial dysfunction, leukocyte migration, extracellular matrix degradation, and platelet activation. We discuss herein blood levels of adhesion molecules, matrix metalloproteases, monocyte chemoattractant protein-1, and tissue factor and interferon-gamma production of circulating T cell in patients with acute coronary syndromes. These biomarkers are associated with not only formation and progression of atherosclerotic plaque but also incidence of coronary event.
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