Description
The Polygenic Risk Map test is a genetic analysis tool that leverages Polygenic Risk Scores (PRS) to evaluate an individual's genetic predisposition to various cardiovascular diseases and related conditions. This test provides healthcare providers with detailed insights into genetic factors that influence the risk of developing cardiovascular diseases, helping to guide early interventions and personalized treatment plans.
Biomarkers Included:
- Ancestry
- Provides information on genetic heritage based on 26 global populations.
- Polygenic Risk Score – Atrial Fibrillation (AF)
- Assesses genetic risk for developing atrial fibrillation, a type of irregular heartbeat that increases the risk of stroke.
- Polygenic Risk Score – BMI (Body Mass Index)
- Estimates genetic predisposition to obesity or being overweight, which is a risk factor for cardiovascular disease.
- Polygenic Risk Score – Coronary Artery Disease (CAD)
- Evaluates the genetic risk for CAD, a condition where the arteries supplying blood to the heart become narrowed or blocked.
- Polygenic Risk Score – High LDL Cholesterol
- Analyzes genetic factors that may predispose an individual to have high LDL cholesterol, often referred to as "bad" cholesterol.
- Polygenic Risk Score – Hypertension
- Assesses genetic risk for high blood pressure, a major risk factor for heart disease and stroke.
- Polygenic Risk Score – Lipoprotein (a)
- Measures genetic predisposition to elevated levels of lipoprotein (a), a particle in the blood associated with an increased risk of cardiovascular diseases.
- Polygenic Risk Score – Low HDL Cholesterol
- Determines the genetic risk of having low HDL cholesterol, which is linked to an increased risk of heart disease.
- Polygenic Risk Score – Triglycerides
- Analyzes the genetic risk for elevated triglyceride levels, which are associated with a higher risk of heart disease.
- Polygenic Risk Score – Type 2 Diabetes
- Estimates the genetic risk for developing type 2 diabetes, which is closely linked to cardiovascular disease.
Why This Test is Important:
Understanding genetic risk factors for cardiovascular conditions allows for personalized prevention and intervention strategies. This test provides valuable insight into a person's risk, enabling healthcare providers to offer more targeted advice, early lifestyle changes, and treatment to prevent or manage cardiovascular diseases more effectively.
Fasting:
Fasting is not required for this test.
