Comprehensive CVD Test

The Comprehensive CVD Test is designed to provide a thorough understanding of your cardiovascular health by analyzing genetic markers linked to common and inherited heart diseases. Cardiovascular disease (CVD) remains one of the leading causes of death globally, and many individuals are unaware of their genetic risk factors until symptoms arise. This test is especially beneficial for individuals with a family history of heart disease, arrhythmias, or other cardiovascular conditions. By offering advanced genetic testing for heart disease, including conditions like cardiomyopathies, arrhythmias, and familial hypercholesterolemia, this test helps you assess your genetic predisposition to heart disease and take preventive actions accordingly.

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Comprehensive CVD Test

The Comprehensive CVD Test is designed to provide a thorough understanding of your cardiovascular health by analyzing genetic markers linked to common and inherited heart diseases. Cardiovascular disease (CVD) remains one of the leading causes of death globally, and many individuals are unaware of their genetic risk factors until symptoms arise. This test is especially beneficial for individuals with a family history of heart disease, arrhythmias, or other cardiovascular conditions. By offering advanced genetic testing for heart disease, including conditions like cardiomyopathies, arrhythmias, and familial hypercholesterolemia, this test helps you assess your genetic predisposition to heart disease and take preventive actions accordingly.

1.Who Should Take the Comprehensive CVD Test?
  • Individuals with a Family History of Heart Disease: If heart conditions like cardiomyopathy, arrhythmias, or coronary artery disease run in your family, this test helps identify your genetic risk and allows for early intervention.
  • Those Concerned About Their Heart Health: Whether you’re experiencing symptoms or simply seeking a heart disease risk test, this genetic analysis provides detailed insights into your cardiovascular risks.
  • Athletes or Fitness Enthusiasts: Gain a better understanding of your genetic predispositions for heart performance and potential risks during intense physical activities with this cardiovascular health test.
  • Patients with Unexplained Heart Symptoms: If you’ve experienced chest pain, irregular heartbeat, or fatigue without a clear diagnosis, this test can uncover genetic clues linked to your condition.
  • Individuals Focused on Preventive Health: As part of a regular cardiovascular check-up, this test provides a proactive approach to managing inherited heart risks.
2.Why is this test important?

Key Reasons to Choose Genetic Testing for Heart Health:

  • Early Detection of Genetic Risks: The test identifies genetic variants linked to inherited cardiac disease and provides insights into conditions like hypertrophic cardiomyopathy and arrhythmias, enabling timely interventions.(4)
  • Personalized Prevention: Tailor lifestyle changes and medical treatments based on your genetic profile, reducing the likelihood of heart disease progression.(5)
  • Enhanced Diagnostic Accuracy: This test complements traditional cardiac diagnostic tests by uncovering genetic factors often missed in routine screenings.
  • Optimized Treatment Plans: By analyzing genetic influences on medication responses, the test aids in selecting the best treatments for cardiovascular conditions.(7)
  • Improved Long-Term Outcomes: Genetic insights empower you to address potential risks, contributing to better overall cardiovascular health and longevity.(6)

Genetic Insight and prevalence in India:

Genetic testing is crucial for diagnosing cardiomyopathies and arrhythmic disorders, with expert guidelines recommending comprehensive evaluation of family history, targeted testing of specific gene panels for conditions like hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), and long-QT syndrome. For long-QT syndrome, genes such as KCNQ1, KCNH2, and SCN5A are critical in diagnosis. Cascade testing for at-risk relatives is also recommended to optimize diagnosis, management, and preventive care.(1)

Familial hypercholesterolemia (FH) is common in people with early heart disease in India, affecting about 15% of patients. To help identify those with FH, routine screening using family history of early heart disease and high cholesterol, along with a simple scoring system, can be an effective way to detect it early.(2)

Familial hypercholesterolemia (FH) is a genetic disorder that causes high LDL cholesterol and early heart disease, often linked to mutations in the LDLR, APOB, and PCSK9 genes. Accurate diagnosis involves careful clinical assessment and genetic testing to differentiate FH from similar conditions, ensuring proper treatment and genetic counseling. (3)

3. DrOmic’s Lab  for Comprehensive CVD Testing:

At DrOmics Labs, we offer advanced cardiac genetic testing through our Comprehensive CVD Test, which provides detailed insights into cardiovascular risks. This test evaluates genetic markers linked to heart conditions like cardiomyopathy, arrhythmias, and coronary artery disease, offering personalized risk assessments. It also helps optimize medication by identifying how your body responds to heart medications, reducing the risk of adverse effects. Additionally, we provide customized lifestyle recommendations on diet, exercise, and preventive care based on your genetic profile to better manage and prevent heart-related issues.

Cardiovascular Diseases Covered by DrOmics Labs Genetic Test Gene
Arrythmias:
Congenital Long QT Syndrome (LQTS) KCNQ1, KCNH2, SCN5A, CALM1, CALM2, CALM3, KCNE1, CACNA1C, KCNJ2, TRDN
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) RYR2, CASQ2, CALM1, CALM2, CALM3, TRDN, TECRL, KCNJ2, SCN5A, PKP2
Brugada Syndrome (BrS) SCN5A
Short QT Syndrome (SQTS) KCNH2, KCNQ1, KCNJ2, SLC4A3
Inherited Atrial Fibrillation (AF) SCN5A, KCNQ1, MYL4, TTN (truncating variants)
cardiomyopathies:
Hypertrophic Cardiomyopathy (HCM) MYH7, MYBPC3, TNNI3, TPM1, MYL2, MYL3, ACTC1, TNNT2, CSRP3, TNNC1, JPH2
Arrhythmogenic Cardiomyopathy (ACM) PKP2, DSP, DSG2, DSC2, JUP, TMEM43, PLN, FLNC, DES, LMNA
Dilated Cardiomyopathy (DCM) BAG3, DES, FLNC, LMNA, MYH7, PLN, RBM20, SCN5A, TNNC1, TNNT2, TTN, DSP, ACTC1, ACTN2, JPH2, NEXN, TNNI3, TPM1, VCL
Left Ventricular Noncompaction Cardiomyopathy (LVNC) MYH7, MYBPC3, TTN, ACTC1
Inherited Thoracic Aortic Disease
Inherited Thoracic Aortic Disease FBN1, LOX, COL3A1, TGFBR1,TGFBR2, SMAD3, TGFB2, ACTA2, MYH11, MYLK, PRKG1
Familial hypercholesterolemia
Familial hypercholesterolemia LDLR, APOB, PCSK9(pediatric)
4. How It Works:
  • Sample Collection: A simple and non-invasive saliva or cheek swab sample is collected for genetic analysis.
  • Laboratory Testing: The collected sample is sent to a certified laboratory, where it is tested for specific genetic markers associated with cardiovascular conditions.
  • Results and Report: After analysis, you will receive a detailed report outlining your genetic predispositions for various cardiovascular diseases, along with personalized recommendations for risk management and prevention.

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Comprehensive CVD Test

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