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Dual antiplatelet therapy with aspirin and thienopyridines is an essential treatment in patients undergoing percutaneous coronary intervention (PCI). However, despite intensified antiplatelet treatment, some of the patients undergoing PCI develop thrombotic stent occlusion, suggesting incomplete platelet inhibition due to thienopyridine resistance. Some patients develop bleeding event because of the improper dosage and covariation. This observational study is designed for clarifying the Influence of gene polymorphism on clinical outcomes in patients undergoing PCI.
Patients undergoing PCI who received dual antiplatelet therapy with both aspirin (100mg) and P2Y12 inhibitors in standard dosage were enrolled. Investigators examined plasma biomarkers for platelet activation and DNA in those patients, and then analyzed the CYP2C19 genetic polymorphism to examine the influence of this genetic variation on the several biomarkers for platelet activation and bleeding event.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| CYP2C19 | Genetic | The CYP2C19 enzyme plays a vital role in the two bioactivation steps of clopidogrel leading to lower (CYP2C19*17 carriers) or higher (CYP2C19*2 carriers) risk of major adverse cardiovascular events. |
| Measure | Description | Time Frame |
|---|---|---|
| Patients with treatment-related major bleeding event as assessed by the Bleeding Academic Research Consortium (BARC) bleeding criteria | The major bleeding event was a composite endpoint of BARC bleeding type 3 and 5), defined according to the BARC bleeding criteria, which was used widely in this field. BARC bleeding was defined as follows: BARC type 1, any bleeding that is not actionable; type 2, any overt, actionable sign of bleeding; type 3a, overt bleeding with a haemoglobin drop of 3-5 g/dL or any transfusion; type 3b, overt bleeding with a haemoglobin drop >5 g/dL, requiring vasopressors, surgical intervention, or due to cardiac tamponade; type 3c, any intracranial or intraocular bleeding; and finally type 5, any bleeding resulting in death (type 4 was coronary artery bypass graft-related bleeding, which was excluded). Investigator will get all the information through regular return visit and telephone follow-up after discharge. | up to 24 months |
| Measure | Description | Time Frame |
|---|---|---|
| Major adverse cardiac events (MACE) | A composite of death, myocardial infarction, stroke, stent thrombosis, and ischemia-driven revascularization | up to 24 months |
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Inclusion Criteria:
Exclusion Criteria:
Inability to provide written informed consent
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PCI patients in Beijing Anzhen Hospital from August 2018 to August 2019
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Yujie Zhou, PhD,MD | Contact | 8613901330652 | azzyj12@163.com |
| Name | Affiliation | Role |
|---|---|---|
| Yujie Zhou, PhD,MD | Beijing Anzhen Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Beijing Anzhen Hospital | Recruiting | Beijing | Beijing Municipality | 100029 | China |
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| ID | Term |
|---|---|
| D065731 | Cytochrome P-450 CYP2C19 |
| ID | Term |
|---|---|
| D065730 | Limonene Hydroxylases |
| D000072467 | Cytochrome P450 Family 2 |
| D003577 | Cytochrome P-450 Enzyme System |
| D003580 | Cytochromes |
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Gene polymorphism is measured by using whole blood in patients undergoing PCI.
| D045762 | Enzymes and Coenzymes |
| D006899 | Mixed Function Oxygenases |
| D010105 | Oxygenases |
| D010088 | Oxidoreductases |
| D004798 | Enzymes |
| D006420 | Hemeproteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |