African-American Pharmacogenetics (AA Genetic)
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Purpose
This is a genetic and platelet reactivity study of African-American versus Caucasian patients undergoing percutaneous coronary intervention and receiving clopidogrel or prasugrel. The investigators aim is twofold: to describe differences in allele frequencies between African-Americans and Caucasians, and to explore associations of platelet reactivity and genetic polymorphisms in these two groups.
| Condition | Intervention |
|---|---|
|
Acute Coronary Syndrome |
Other: Genotyping and platelet reactivity testing with the VerifyNow P2Y12 assay |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | African-American Pharmacogenetics |
- Distribution of CYP polymorphisms [ Time Frame: During hospital stay; average hospital stay is less than 48 hours ] [ Designated as safety issue: No ]CYP polymorphisms will be classified by their known effects upon enzyme function, using the consensus star-allele nomenclature. More specifically, patients will be classified as a "poor metabolizer" if they possess at least one CYP allele known to be associated with reduced function of that particular CYP enzyme. Allele frequencies will then be compared between African-american and Caucasian patients.
- Platelet reactivity [ Time Frame: During hospital stay; average hospital stay is less than 48 hours ] [ Designated as safety issue: No ]The secondary exploratory objective is to assess for associations between "poor metabolizer" CYP genotypes and the levels of post-thienopyridine platelet reactivity.
| Estimated Enrollment: | 200 |
| Study Start Date: | November 2011 |
| Estimated Study Completion Date: | June 2014 |
| Estimated Primary Completion Date: | June 2014 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| African-American on clopidogrel |
Other: Genotyping and platelet reactivity testing with the VerifyNow P2Y12 assay
All patients will undergo genotyping and platelet reactivity testing with the VerifyNow P2Y12 assay, at least 6 hours after receiving a thienopyridine loading dose but before hospital discharge.
|
| African-American on prasugrel |
Other: Genotyping and platelet reactivity testing with the VerifyNow P2Y12 assay
All patients will undergo genotyping and platelet reactivity testing with the VerifyNow P2Y12 assay, at least 6 hours after receiving a thienopyridine loading dose but before hospital discharge.
|
| Caucasian on clopidogrel |
Other: Genotyping and platelet reactivity testing with the VerifyNow P2Y12 assay
All patients will undergo genotyping and platelet reactivity testing with the VerifyNow P2Y12 assay, at least 6 hours after receiving a thienopyridine loading dose but before hospital discharge.
|
| Caucasian on prasugrel |
Other: Genotyping and platelet reactivity testing with the VerifyNow P2Y12 assay
All patients will undergo genotyping and platelet reactivity testing with the VerifyNow P2Y12 assay, at least 6 hours after receiving a thienopyridine loading dose but before hospital discharge.
|
Detailed Description:
The investigators propose a pharmacogenetic cohort study of 100 African-American versus 100 Caucasian patients presenting with an acute coronary syndrome, receiving clopidogrel or prasugrel and undergoing PCI. The study will have four arms: African-American on clopidogrel; African-American on prasugrel; Caucasian on clopidogrel; and Caucasian on prasugrel. All patients will undergo genotyping and platelet reactivity testing with the VerifyNow P2Y12 assay, at least 6 hours after receiving a thienopyridine loading dose, but before hospital discharge. All patients will be treated with aspirin 325 mg/day as well.
Race determination will be based on a patient's self-report, but patients enrolled in the trial must also report that all four of their grandparents were of the same race as theirs. Other races (Asian, Native American, et al) will be excluded from this study.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
African-american versus Caucasian patients undergoing percutaneous coronary intervention and receiving clopidogrel or prasugrel.
Inclusion Criteria:
- Patients age 18 or older, of both genders
Presenting with an ACS, defined as at least two of the following:
- symptoms consistent with myocardial ischemia;
- ST segment elevation or depression of at least 1 mm in 2 or more contiguous leads on EKG;
- a cardiac troponin I level above upper limit of normal.
Self-reported African-american or Caucasian race
a. all 4 grandparents of same race
- No contraindications to prasugrel therapy.
- Patient is scheduled for, or has already undergone, PCI.
Exclusion Criteria:
- Known allergies to aspirin, clopidogrel, or prasugrel.
- Patient known to be pregnant or lactating.
- Patient with known history of bleeding diathesis or currently active bleeding.
- Platelet count <100,000/mm at the time of enrollment.
- Hematocrit <25% at the time of enrollment.
- On warfarin therapy at the time of PCI, or patient likely to require warfarin therapy post-PCI.
- Received fibrinolytics within the past 48 hours.
- Received a glycoprotein IIb/IIIa inhibitor within the past 48 hours, or if such a strategy for PCI involving a glycoprotein IIb/IIIa inhibitor is planned.
- Taking maintenance thienopyridine therapy in the previous 5 days.
- Known blood transfusion within the preceding 10 days.
- Patients treated with non-steroidal anti-inflammatory drugs (NSAIDS) within the previous 5 days.
- Patients with known chronic liver disease.
- Age greater than 75 years
- Body weight less than 60 kg
- History of stroke or transient ischemic attack
- Surgery planned within 1 month
- Patient likely to require coronary artery bypass grafting
- Any significant medical condition that, in the investigator's opinion, may interfere with the patient's optimal participation in the study.
Contacts and Locations| United States, District of Columbia | |
| Washington Hospital Center | Recruiting |
| Washington, District of Columbia, United States, 20010 | |
| Contact: Ron Waksman, MD 202-877-5975 ron.waksman@medstar.net | |
| Principal Investigator: Ron Waksman, MD | |
| Principal Investigator: | Ron Waksman, MD | Medstar Research Institute |
More Information
No publications provided
| Responsible Party: | Medstar Research Institute |
| ClinicalTrials.gov Identifier: | NCT01408121 History of Changes |
| Other Study ID Numbers: | AA Genetic |
| Study First Received: | July 29, 2011 |
| Last Updated: | February 14, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Medstar Research Institute:
|
Platelet reactivity Genotyping |
Additional relevant MeSH terms:
|
Acute Coronary Syndrome Myocardial Ischemia Heart Diseases Cardiovascular Diseases Angina Pectoris |
Vascular Diseases Chest Pain Pain Signs and Symptoms |
ClinicalTrials.gov processed this record on May 16, 2013