Molecular Contrast Agents for Post-infarct Cardiac Remodeling: A Contemporary Review
Abstract Myocardial infarction (MI) is a leading cause of mortality, affecting 3.8% of the global population under 60 years of age, and 9.5% over 60 years. Adverse post-MI remodeling is the main contributor to heart failure, conferring a three to six-fold increase in risk of premature death. Current imaging modalities such as nuclear imaging and magnetic resonance imaging provide structural and functional information of the heart, and identify extracellular expansion for indirect estimation of infarct size. However, they do not characterise the exact biological mechanisms involved, nor staging of disease progression. Molecular imaging aims to visualise the underlying processes of remodeling at a molecular and cellular level, aiding more accurate prognosis and targeted treatment. Molecular tracers, such as radioisotopes and paramagnetic nanoparticles, are modified to adhere to specific molecules or cells involved in inflammation, angiogenesis and scar formation, which can be visualised and quantitatively assessed using positron-emission tomography and magnetic resonance imaging. This article provides an overview of the pathophysiology of adverse remodeling, the latest molecular contrast agents under development, and future directions for integration into clinical practice.
Authors
- W. D. Watson (ORCID: https://orcid.org/0000-0002-2279-6594)
- Pak Yin Lam (ORCID: https://orcid.org/0000-0002-1003-5755)
- Jason M. Tarkin (ORCID: https://orcid.org/0000-0002-9132-120X)
- Ziad Mallat
Publication Details
- Journal
- Apollo (University of Cambridge)
- Published
- 2025-11-03
- Primary Topic
- Cardiac Fibrosis and Remodeling
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Wellcome Trust
- National Institute for Health and Care Research
- British Heart Foundation
- NIHR Cambridge Biomedical Research Centre