Identifying specific hazard patterns for emerging cardiovascular disease

Identifying specific hazard patterns for emerging cardiovascular disease

Predicting when atherosclerotic changes in the arteries in a stable state will progress to acute cardiovascular disease has remained unresolved. The authors of the paper currently published in Nature Communications, led by first author Prof. Ulrich Flögel, MD, Institute of Molecular Cardiology, Faculty of Medicine, Heinrich Heine University, Düsseldorf, Germany, present an imaging technique—the targeted and multicolor nanotracer platform technology—that visualizes the hazard patterns in the development of progressive coronary disease in a mouse model.

Hazard pattern using the example of a mouse heart (top in cross-section) with a massively worn out and thus in its performance strongly impaired right heart as consequential damage to be seen in the follow-up examination (bottom right compared to bottom left).

The cascade of these vascular diseases ranges from inflammation of the vessel, thrombosis with subsequent detachment of minute particles of the vascular plaque, to vascular occlusion resulting in permanent damage due to, for example, myocardial infarction.

To show the hazard patterns, three molecules (ligands)—are coupled to different types of perfluorocarbon nanoemulsion. They are specifically directed respectively to sites of inflammation, acute and chronic thrombi. There, they embed themselves and become visible and distinguishable through the use of a specific MRI imaging technique (19F-MRI).

This enables the scientists to identify areas that are at high risk of developing a heart attack. This happens at a time when no conventional parameter in laboratory diagnostics or ECG indicates an imminent danger. The research team shows that these patterns can be visualized reliably—and before the onset of infarction—by the “multi-color multi-targeted 1H/19F MRI” technique they developed. Only a single MRI scan is required, which can localize individually affected sites and differentiate them by color with respect to inflammation, freshly developed or advanced thrombi.

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