Even today, less than 30% of participants in clinical studies in cardiology are women.
That means that most heart disease medications were tested and calibrated based on studies where women were underrepresented.
And yet women report adverse side effects more than men do. For example, anticoagulants used to reduce the risk of embolism lead to a higher incidence of bleeding in women. Why? Because a person’s response to medication can vary depending on their genetics, weight, size, metabolism, even kidney function.
Dr. de Denus’s project examines the concentrations and effects of nearly 50 cardiovascular medications in 10,000 patients of the MHI Biobank (a repository of health-related information and biological samples that is one of the largest hospital cohorts in the world).
The goal is to determine why women are more at risk of adverse side effects and if dosages can be optimized depending on their individual traits.
The project assesses if adjustments based on sex, weight, genetics, or kidney function could improve the tolerance and efficacy of treatments.
By taking a closer look at the concentrations of cardiovascular drugs, this precision medicine project could transform the way treatments are prescribed. The goal is to adapt dosages to individual profiles and: