Precision Medicine
Genomic testing for implications on cardiac health
Why should you opt for genomic testing?

Heart disease is one of the leading causes of death worldwide. The risk of developing a heart disease can be associated with a lot of factors, including the individual’s genetic makeup. Identification of the genetic changes that can put you at risk of developing a cardiac condition helps prevent, control or manage the disease, not only for you but also your family. It can provide lifesaving information about your heart condition and assess your response to certain medications which are used to treat it.

Genomic profiling may serve as a valuable tool to predict the risk of recurrence, understand the inheritance of the condition within a family, and evaluate the need for family screening. It carries the potential to improve quality of life and life expectancy by providing valuable information with respect to personalized medical care and confidence in the clinical diagnosis.

Personome’s Cardiac Genomic Profiling

Personome’s Cardiac Genomic Profiling uses latest molecular analysis technologies to analyze specific molecular defects associated with an increased risk of developing certain cardiac conditions. Our tests assess the biomarkers associated with the following:

  • Arrhythmia & Cardiomyopathy
  • Familial Hypercholesterolemia
  • Congenital Heart Disease
  • Pharmacogenomics

Personome enables you and your doctor to make informed decisions about your body’s response to commonly used cardiovascular drugs, changes necessary to your lifestyle, diet and exercise. The tests are non-invasive, rapid and accurate. Our high throughput methods along with integrated evidence based clinical and drug data, makes a comprehensive and reliable report that helps you and your physician devise a personalized treatment plan and lifestyle changes for your cardiac health.