Comprehensive PGx Test: Revolutionizing Personalized Medicine
The Comprehensive PGx Test decodes how your genetic makeup affects your response to medications. Designed to address critical chronic conditions like cardiovascular diseases, cancer, neurological disorders, and diabetes, it analyzes over 100 genes and thousands of single nucleotide polymorphisms (SNPs). This empowers healthcare providers to prescribe safer and more effective treatments tailored to your genetic profile.
Why Is the Comprehensive PGx Test Important?
1. Who Should Take the Test?
- Family History: Individuals with inherited risks for cardiovascular diseases, cancer, neurological disorders, or diabetes.
- Medication Challenges: Those experiencing adverse drug reactions (ADRs) or suboptimal treatment outcomes.
- Chronic Health Issues: People managing conditions like chest pain, cognitive decline, unstable glucose levels, or tumor recurrence.
2. The Seriousness of Chronic Conditions
Chronic illnesses are leading causes of death worldwide. Despite medical advancements, variability in drug response often leads to treatment failures or adverse drug reactions. These variations are influenced by genetic factors critical to drug metabolism and efficacy.
3. Why Do These Health Problems Happen?
Chronic conditions stem from genetic predispositions, environment, and lifestyle. Genetics influence processes such as:
- How your body metabolizes drugs (pharmacokinetics).
- How drugs act on your body (pharmacodynamics).
- Likelihood of adverse reactions to specific medications.
Examples:
- Cardiovascular Diseases: Genetic variants in SLCO1B1 affect statin tolerance; others influence responses to blood thinners like clopidogrel.
- Cancer: Mutations alter chemotherapy drug effectiveness, requiring personalized treatment.
- Neurological Disorders: Variants in CYP2D6 affect metabolism of antidepressants, antipsychotics, and antiepileptics.
- Diabetes: Genetic factors impact insulin sensitivity and glucose-lowering medication efficacy.
How DrOmics Addresses These Needs
- Integrated Approach: Combines genetic sequencing with clinical expertise for comprehensive insights.
- Personalized Reports: Clear and actionable insights for patients and healthcare providers.
- Proactive Solutions: Enables informed decisions, risk reduction, and improved long-term outcomes.
Unique Selling Points (USPs)
- Broad Therapeutic Coverage: Integrates Cardio PGx, Onco PGx, Neuro PGx, and Diabetes PGx into one test.
- Evidence-Based Design: Adheres to PharmGKB and CPIC guidelines for accuracy.
- Extensive Genetic Analysis: Evaluates 100+ genes and over 1,000 SNPs.
- Non-Invasive Sampling: Simple saliva collection for convenience.
- Rapid Turnaround: Reports delivered within days for timely intervention.
- Cost Efficiency: Minimizes healthcare expenses by optimizing treatments.
Categories Analyzed in the Comprehensive PGx Test
- Cardio PGx: Optimizes treatments for heart conditions using 350+ SNPs.
- Onco PGx: Enhances safety and efficacy of cancer therapies using 40+ SNPs.
- Neuro PGx: Personalizes medications for neurological disorders with 25+ SNPs.
- Diabetes PGx: Guides glucose-lowering medications and insulin therapy with 20+ SNPs.
How Does the Comprehensive PGx Test Work?
- Sample Collection: Provide a saliva sample using the DrOmics kit.
- Genetic Analysis: Next-generation sequencing evaluates genes and SNPs for drug response.
- Report Generation: A detailed report highlights variations, recommendations, and risks.
- Clinical Application: Insights are used to tailor treatment plans with healthcare providers.
Choose the DrOmics Comprehensive PGx Test to unlock the power of your genetics and embrace precision-driven healthcare. Achieve optimal health outcomes while minimizing risks associated with standard treatments.
Reviews
There are no reviews yet.