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LABORATORIES Exceltox offers an extensive menu of testing for cardiac disorders that can help determine the risk of thrombosis or prothrombin deficiency to ultimately guide therapy decisions for commonly prescribed drugs for cardiovascular disease. The Exceltox panel for genetic and pharmacogenetic testing of cardiac disorders includes: • Factor II (Prothrombin) • Factor V Leiden (Inherited Thrombophilia) • CYP450 2C19 platelet inhibitor metabolism • CYP450 2D6 beta blocker metabolism • Warfarin sensitivity LABORATORIES MOLECULAR PROFILING FOR CARDIAC DISORDERS Know a patient's molecular genotype for cardiac disorders and response to cardiac therapies.

Cardiac Disorder PGX Brochure

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Page 1: Cardiac Disorder PGX Brochure

L A B O R A T O R I E S

Exceltox offers an extensive menu of testing

for cardiac disorders that can help

determine the risk of thrombosis or

prothrombin deficiency to ultimately guide

therapy decisions for commonly prescribed

drugs for cardiovascular disease.

The Exceltox panel for genetic and

pharmacogenetic testing of cardiac disorders includes:

• Factor II (Prothrombin)• Factor V Leiden (Inherited Thrombophilia)• CYP450 2C19 platelet inhibitor metabolism• CYP450 2D6 beta blocker metabolism• Warfarin sensitivity

L A B O R A T O R I E S

MOLECULAR PROFILING FOR

CARDIAC DISORDERS

Know a patient's molecular genotype for cardiac disorders

and response to cardiac therapies.

Page 2: Cardiac Disorder PGX Brochure

Comprehensive Testing for Cardiac Disorders

Factor II and Factor V Leiden

Factor II and Factor V are important components of the coagulation cascade. Testing for Factor ll and Factor V Leiden mutations provides important information in a differential diagnosis for the clinical presentation of thrombophilia. Factor V is the most common variant associated with inherited thrombosis, with a population frequency ranging from 3-8% in the United States. Factor II is the second most common mutation -- present in 1-2% of the general population.

Based on the dominant mode of inheritance, the testing of direct family members (parents, siblings and children) is strongly recommended.

Warfarin Sensitivity

Warfarin interferes with the recycling of Vitamin K, which can result in reduced activation of several clotting factors and diminished clotting ability. Consequently, bleeding complications are a highly prevalent cause of morbidity and mortality in patients who receive warfarin.5

A recent study revealed that warfarin genotyping reduced the risk of hospitalization due to thromboembolism or bleeding in outpatients. It concluded that genotyping should be strongly considered in patients beginning warfarin treatment.6

According to the FDA, all patients who are candidates for Coumadin (warfarin) therapy should be tested for their genotype prior to initiating treatment.7

CYP450 2C19 and 2D6

Plavix® (clopidogrel) is the world’s second most prescribed drug. Variation in Cytochrome P450 2C19-mediated metabolism is a key source of variability underlying patient reaction to Plavix (clopidogrel).1

CYP450 D6 testing may also be considered medically necessary for patients with cardiovascular disease who are undergoing treatment with certain drugs.

According to recent studies, genetic testing for variations in CYP2D6 and CYP2C19 may result in improved patient management, a decrease in episodes of drug toxicity, drug selection and/or dosage adjustment informed by genetic testing for variations in CYP250 2C19 and 2D6 may also enable improved pain and fewer adverse drug interactions.2-4

References

1. Mega, et al. JAMA. 2010;304:1821-30. 2. Jannetto PJ, Bratanow NC. Pain management in the 21st century. Expert Opin Drug Metab Toxicol.

2011;7:745-752. 3. De Gregori M, Allegri M, De Gregori S, et al. How and why to screen for CYP2D6 interindividual variability in patients under

pharmacological treatments. Curr Drug Metab. 2010;11:276-282. 4. Rollason V, Samer C, Piguet V, et al. Pharmacogenetics of analgesics.

Pharmacogenomics. 2008;9:905-933. 5. Wysowski D, et al. Bleeding Complications With Warfarin Use. Arch Intern Med

2007;167(13):1414-1419. 6. Epstein et al. Warfarin Genotyping Reduces Hospitalization Rates. J Am Coll. Cardiol; 2010;55:2804-12. 7. FDA,

Black Box Warning, Coumadin, October 2006.

Benefits of Genetic and Pharmacogenetic Testing for Cardiac Disorders:

Knowing a patient's molecular profile for cardiac disorders and their response to cardiac therapies.

That’s personalized medicine, powered by Exceltox for cardiac disorders.

• Genetic testing with Factor II and Factor V Leiden

may provide important information in a differential diagnosis for the clinical presentation for thrombophilia.

• Pharmacogenetic testing information adheres to FDA guidelines that require genotyping prior to initiating treatment.

• Pharmacogenetic testing for cardiac disorders may help physicians implement the appropriate drug and dosage to minimize the risk of minor to life threatening reactions and ensure optimal response.

DCO 011-001 8/27/14

L A B O R A T O R I E S

Excellence in Science, Service, & Results.

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