Traditionally, CVD treatments have been nonspecific, treating all patients similarly. Precision medicine is allowing us to better understand these differences, especially as genetic data reveal diverse types of cardiomyopathies — conditions that affect the muscle of the heart.
We are working to tailor CVD treatments to patient subgroups based on unique genetic traits. This precise approach is rooted in causal human biology, and we are leveraging insights from our work in hypertrophic cardiomyopathy (HCM) — where we developed a novel, first-in-class medicine that works directly on the heart —to put forward new ways of treating certain types of patients with heart failure. These efforts aim to both help improve clinical outcomes, such as a reduction in hospitalizations as example, and also improve quality of life.