We examine your unique biology as a category of one to reveal insights that traditional methods may miss.
Americans have a heart attack
each year
is how often someone in the U.S. experiences a heart attack
heart attacks are silent, occuring without warning
Coronary heart disease (CHD) is the leading cause of death in the U.S., responsible for nearly 1 in every 3 deaths. Each year, more than 800,000 Americans experience a heart attack, and for many, it is the first sign of underlying disease.
While CHD generally results from a build up of plaque in the arteries of the heart, CHD and heart attacks can also occur when the arteries are not severely blocked. One example is Ischemia with No Obstructive Coronary Arteries (INOCA). INOCA is particularly common in women and happens when blood flow to the heart is reduced without major plaque build up or visible blockages.
Plaque build-up and the presence of traditional risk factors like high blood pressure, diabetes, or high cholesterol are important to know, but they don’t fully capture heart disease.
Learn More About CHD
of those who experience a coronary heart disease event were previously deemed low risk by standard assessments
of those with CHD do not have traditional risk factors
of coronary artery disease are missed by tests like stress EKG, SPECT and stress echo
Your DNA is your genetic blueprint, the code you are born with. But genetics accounts for less than 20% of heart disease risk.
The larger influence comes from epigenetics, which is how your environment, lifestyle, and everyday experiences affect how your genes are expressed. Epigenetics acts like the switchboard that controls whether certain genes linked to heart disease are turned on or off.
That means your heart disease risk isn’t fixed at birth. It shifts and changes over time, depending on both your genetics and the world around you.
By combining genetics and epigenetics with artificial intelligence, our tests deliver a more complete and precise view of your heart health than traditional methods alone.
Our Technology
Rx Only FSA/HSA Eligible
A blood test that predicts your three-year risk of a coronary heart disease event, including a heart attack
Rx Only FSA/HSA Eligible
A blood test that can detect the presence of coronary heart disease and help inform personalized treatment
By combining epigenetics with AI, our tests go beyond traditional tests to measure your unique molecular biology.
Our blood tests do not require fasting or exposure to radiation that could increase cancer risk.
Our technology combines epigenetics, genetics, and AI to more comprehensively assess heart health even in the absence of risk factors.
Our tests are clinically validated, backed by peer-reviewed publications, and have high sensitivity and specificity.
Samples can be collected via phlebotomy in a clinical setting or patients can request a test virtually and collect their sample at home.
Our tests must be prescribed by a licensed healthcare provider. Request your at-home test through our independent telemedicine partner.
After a healthcare provider orders the test, you’ll receive an at-home kit with materials to collect and ship your sample.
Results will be ready within 10 business days of your sample arriving at our lab. The healthcare provider will share results and is available for a follow up consultation.
