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Published on: January 28, 2020
Beyond cholesterol: targeting inflammatory biomarkers in cardiovascular disease
Qamar Abuhassan1, Tamara Nazar Saeed2, Ali Fawzi Al-Hussainy3
1Department of Pharmaceutics and Pharmaceutical Technology, School of Pharmacy, University of Jordan, Amman 11942, Jordan.
Insights
Cardiovascular disease (CVD) is driven by inflammation, not just lipids. Targeting inflammation with therapies like IL-1β inhibition can reduce cardiovascular events, offering new prevention strategies.
Area of Science:
- Cardiology and Immunology
- Biomarkers and Therapeutics
Background:
- Cardiovascular disease (CVD) is a leading global cause of death.
- Inflammation is a key factor in CVD development and complications.
- Current lipid-lowering therapies leave a residual inflammatory risk.
Purpose of the Study:
- To review inflammatory biomarkers in CVD.
- To examine the role of inflammation in atherosclerosis and thrombosis.
- To discuss inflammation-targeted therapies for CVD prevention.
Main Methods:
- Narrative review of current scientific literature.
- Synthesis of data on inflammatory biomarkers (hsCRP, IL-6, TNF-α, MPO).
- Analysis of clinical trial evidence for anti-inflammatory treatments.
Main Results:
- Inflammation plays a central role in CVD pathogenesis.
- Targeting inflammation (e.g., IL-1β inhibition, colchicine) reduces cardiovascular events independently of lipid lowering.
- Emerging multi-omics signatures offer new insights.
Conclusions:
- CVD should be viewed as a lipid-inflammatory disorder.
- Inflammation-targeted strategies represent a promising complement to existing CVD therapies.
- Integrating inflammatory biomarkers can enhance risk stratification and precision medicine.
Abstract:
Cardiovascular disease (CVD) remains the leading cause of morbidity and mortality worldwide, and increasing evidence has demonstrated that inflammation is a central driver of CVD initiation, progression, and clinical complications. While cholesterol-lowering therapies have transformed CVD prevention, a substantial residual inflammatory risk persists even in optimally treated patients, underscoring the need to move beyond lipid-centric paradigms. This narrative review synthesizes current knowledge on key inflammatory biomarkers including high-sensitivity C-reactive protein (hsCRP), interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), myeloperoxidase (MPO), and emerging multi-omics-derived signatures and examines their mechanistic roles in atherosclerotic plaque formation, endothelial dysfunction, and thromboinflammatory pathways. We highlight evidence from major clinical trials demonstrating that targeted modulation of inflammatory pathways, such as IL-1β inhibition and colchicine therapy, can reduce cardiovascular events independent of lipid lowering. Additionally, we discuss the translational challenges and opportunities in integrating inflammatory biomarkers into risk stratification, precision therapeutics, and clinical decision-making. By highlighting CVD as a lipid-inflammatory disorder, this review emphasizes the potential of inflammation-targeted strategies to complement existing therapies and reshape future cardiovascular prevention.
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