The goal of this study is to determine how your genetic risk influences health decisions and other things that can be controlled in life. Our first genetic risk score is calculated for coronary artery disease (CAD).
CAD ultimately leads to heart attacks, heart failure and sometimes sudden cardiac death and is the main reason heart disease remains as the number one cause of death worldwide. Other researchers have shown that this genetic risk score can be used to identify people with low, intermediate, and high risk for coronary heart disease. It has also been shown that the use of statins (cholesterol lowering drugs) provides greater benefit and protection against heart attack for people with high genetic risk for coronary artery disease.
Many conditions affecting our health are caused by a combination of our
environment, our behaviors, and our genes. While we can alter some factors
in our lives to reduce our chances of developing different diseases (e.g.,
not smoking cigarettes), the contribution from our genetic risk encoded by
our DNA remains with us throughout our lives. Scientists are still trying
to determine the entirety of genetic factors that influence disease, but
for some conditions it has been shown that the factors identified thus
far can begin to identify people at high to low genetic risk. Looking across
your genome, we can calculate your cumulative genetic risk score – which
can be used to rank your genetic risk compared to the other worldwide
To join this study, you must meet the following criteria
- Be 18 years of age or older
- Must have access to your genetic data from 23andMe
- Allow us to access to your genetic data