Comprehensive Cardio PGx

The Comprehensive PGx Test is an all-encompassing pharmacogenomics solution that decodes how your genetic makeup affects your response to medications. This groundbreaking test is designed to address critical chronic conditions such as cardiovascular diseases, cancer, neurological disorders, and diabetes by analyzing over 100 genes and thousands of single nucleotide polymorphisms (SNPs). It empowers healthcare providers to prescribe safer and more effective treatments tailored to your unique genetic profile.
The test involves a non-invasive saliva sample collection, which is processed using advanced genetic sequencing techniques. The results offer actionable insights into drug efficacy, potential side effects, and personalized treatment plans.

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Comprehensive Cardio PGx Test

The Comprehensive Cardio PGx test is a state-of-the-art genetic testing solution designed to revolutionize cardiovascular healthcare by integrating precision medicine into the management and prevention of heart disease.
This test analyzes genetic variations that influence susceptibility to cardiovascular conditions such as:

  • Congestive heart failure
  • Cardiomyopathy
  • Atherosclerotic cardiovascular disease
  • Inherited heart disorders

By identifying genetic predispositions and pharmacogenomic markers, this test empowers clinicians and patients with actionable insights to optimize treatments, manage symptoms effectively, and mitigate cardiovascular disease risk factors.

Who Should Consider Comprehensive Cardio PGx?

This test is ideal for individuals who:

  • Have a family history of genetic cardiac disorders or inherited heart disease.
  • Struggle with medication side effects or poor responses to treatments for heart failure.
  • Are managing cardiovascular disease symptoms like chest pain, shortness of breath, or fatigue.
Why is Genetic Testing for Heart Disease Treatment Outcomes Critical?

In India, approximately 30 million people are affected by coronary heart disease (CHD), and by 2030, CVD-related deaths are expected to rise to 4.2 million.
Genetic testing uncovers these predispositions, enabling early interventions and personalized treatments.

Statin-Related ADRs: Indians metabolize statins differently, which can affect drug levels and increase the risk of adverse effects.
The SLCO1B1 gene variant is present in around 15% of Indians, leading to statin intolerance.

Clopidogrel Resistance: Resistance to clopidogrel is observed in 15.4% of Indian patients, significantly affecting the drug’s efficacy in preventing cardiovascular events.

Key Reasons for Genetic Testing

  • Avoid incorrect medications by ensuring precise prescriptions.
  • Prevent adverse drug reactions (ADRs) like statin intolerance or blood thinner issues.
  • Timely treatment through early detection of genetic risks.
  • Reduce risk of complications such as stroke and arrhythmia.
  • Optimize prevention through targeted genetic insights.

How Does It Work?

  1. Sample Collection: A simple DNA sample, typically from a cheek swab.
  2. Comprehensive Analysis: Genetic markers are analyzed for inherited risks.
  3. Actionable Results: Receive a detailed report with personalized recommendations.
  4. Consultation: Review results with a specialist for tailored treatment plans.

About DrOmics Labs

At DrOmics Labs, we are dedicated to bringing cutting-edge science and personalized healthcare together.
Our Comprehensive Cardio PGx Test offers innovative heart health DNA analysis to provide crucial insights into your cardiovascular health.

Why Choose DrOmics Labs?
  • Personalized Medicine: Tailored insights for managing cardiovascular conditions.
  • Medication Optimization: Precise therapies based on your DNA.
  • Early Detection: Proactively address risks and symptoms.
  • Evidence-Based Design: Scientifically validated insights for improved outcomes.

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Comprehensive Cardio PGx

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