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Molecular signatures of atherosclerotic plaques: An up-dated panel of protein related markers
S Eslava-Alcon1, M J Extremera-García1, A González-Rovira1
1Biomedicine, Biotechnology and Public Health Department, Cadiz University, Spain; Institute of Biomedical Research Cadiz (INIBICA), Spain.
Insights
Identifying vulnerable atherosclerotic plaques is crucial for preventing heart attacks and strokes. Researchers propose a panel of 76 proteins as a potential signature for plaque instability, aiding risk assessment.
Area of Science:
- Cardiovascular Research
- Proteomics
- Biomarker Discovery
Background:
- Atherosclerosis is a leading cause of ischemic events like myocardial infarction and stroke.
- Plaque rupture and arterial blockage are primary drivers of these events.
- Identifying high-risk plaques is essential for timely patient intervention.
Purpose of the Study:
- To address the challenge of identifying vulnerable atherosclerotic plaques.
- To propose a multi-protein signature for assessing plaque instability.
- To improve risk stratification for patients with atherosclerosis.
Main Methods:
- Review and selection of proteins from proteomic studies on unstable atherosclerotic plaques.
- Identification of 76 candidate proteins based on presence in at least two studies.
- Focus on both classical inflammatory and newly identified molecular markers.
Main Results:
- A comprehensive panel of 76 proteins associated with atherosclerotic plaque instability was curated.
- This panel includes diverse markers, from inflammatory proteins to novel candidates.
- The selected proteins have been identified in multiple proteomic analyses of unstable plaques.
Conclusions:
- A single molecular marker is insufficient to predict plaque rupture due to disease complexity.
- A panel of 76 proteins offers a more accurate prognostic signature for plaque instability.
- This protein signature could enhance the identification of patients at risk of occlusive events.
Abstract:
Atherosclerosis remains the leading cause of ischemic syndromes such as myocardial infarction or brain stroke, mainly promoted by plaque rupture and subsequent arterial blockade. Identification of vulnerable or high-risk plaques constitutes a major challenge, being necessary to identify patients at risk of occlusive events in order to provide them with appropriate therapies. Clinical imaging tools have allowed the identification of certain structural indicators of prone-rupture plaques, including a necrotic lipidic core, intimal and adventitial inflammation, extracellular matrix dysregulation, and smooth muscle cell depletion and micro-calcification. Additionally, alternative approaches focused on identifying molecular biomarkers of atherosclerosis have also been applied. Among them, proteomics has provided numerous protein markers currently investigated in clinical practice. In this regard, it is quite uncertain that a single molecule can describe plaque rupture, due to the complexity of the process itself. Therefore, it should be more accurate to consider a set of markers to define plaques at risk. Herein, we propose a selection of 76 proteins, from classical inflammatory to recently related markers, all of them identified in at least two proteomic studies analyzing unstable atherosclerotic plaques. Such panel could be used as a prognostic signature of plaque instability.
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