Molecular imaging of cardiac remodelling after myocardial infarction

Daniel Curley1, Begoña Lavin Plaza2,3, Ajay M Shah4,5

  • 1GKT School of Medicine, King's College London, London, UK.

Insights

Novel molecular imaging techniques offer insights into cardiac repair after myocardial infarction, aiding potential diagnosis and prognosis. However, clinical translation requires extensive multi-center trials for validation.

Area of Science:

  • Cardiovascular Medicine
  • Molecular Imaging
  • Biomedical Engineering

Background:

  • Myocardial infarction (MI) and heart failure pose significant health burdens with high mortality.
  • Cardiac recovery post-MI involves complex molecular pathways, failure of which leads to adverse remodeling.
  • Current imaging lacks insight into molecular repair mechanisms, limiting prognostic capabilities.

Purpose of the Study:

  • To explore the potential of novel molecular imaging techniques for visualizing cardiac repair pathways post-MI.
  • To assess the diagnostic and prognostic value of these advanced imaging modalities.
  • To bridge the gap between preclinical findings and clinical application.

Main Methods:

  • Utilizing advanced imaging modalities like SPECT, PET, and MRI.
  • Employing imaging probes targeting molecular processes such as apoptosis, necrosis, inflammation, angiogenesis, and scar formation.
  • Focusing on visualizing specific molecular pathways involved in cardiac tissue repair.

Main Results:

  • Preclinical studies show promising results for molecular imaging in assessing cardiac repair.
  • These techniques can visualize key biological processes crucial for myocardial recovery.
  • Challenges exist in translating these promising preclinical findings to clinical settings.

Conclusions:

  • Molecular imaging holds potential for enhanced diagnosis and prognosis in post-MI patients.
  • Further multi-center clinical trials are essential to establish diagnostic and prognostic value.
  • Cost-effective clinical translation remains a significant hurdle for widespread adoption.

Related Concept Videos

Nucleosome Remodeling02:54

Nucleosome Remodeling

Nucleosomes are the basic units of chromatin compaction. Each nucleosome consists of the DNA bound tightly around a histone core, which makes the DNA inaccessible to DNA binding proteins such as DNA polymerase and RNA polymerase. Hence, the fundamental problem is to ensure access to DNA when appropriate, despite the compact and protective chromatin structure.
Nucleosome remodeling complex
Eukaryotic cells have specialized enzymes called ATP-dependent nucleosome remodeling enzymes. These enzymes...
11.3K
Bone Remodeling01:40

Bone Remodeling

Bone remodeling is a continuous and balanced process of bone resorption by osteoclasts and bone formation by osteoblasts. In adults, it helps maintain bone mass and calcium homeostasis. While mechanical stress can stimulate turnover as part of the normal maintenance and reparative process, several hormones also regulate bone remodeling.
40.5K
Osteoclasts in Bone Remodeling01:31

Osteoclasts in Bone Remodeling

Osteoclasts are cells responsible for bone resorption and remodeling. They originate from hematopoietic progenitor cells present in the bone marrow. Numerous progenitor cells fuse to form multinucleated cells, each with 10-20 nuclei. A single osteoclast has a diameter of 150 to 200 µM. These cells have ruffled borders that break down the underlying bone tissue and release minerals such as calcium into the blood in bone resorption. Osteoclasts cling to bones with their ruffled edges during...
4.3K
Molecular Models02:00

Molecular Models

Physical models representing molecular architectures of chemical compounds play essential roles in understanding chemistry. The use of molecular models makes it easier to visualize the structures and shapes of atoms and molecules.
44.0K
Molecular Orbital Theory II03:51

Molecular Orbital Theory II

Molecular Orbital Energy Diagrams
27.7K
Molecular Orbital Theory I02:35

Molecular Orbital Theory I

Overview of Molecular Orbital Theory
47.8K