Impact of Renal Function on Ticagrelor-Induced Antiplatelet Effects in Coronary Artery Disease Patients
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- platelet reactivity units
研究概览
简要总结
Dual antiplatelet therapy consisting in aspirin and clopidogrel is the cornerstone of the treatment of the prevention of the thrombotic events in patients with coronary artery disease (CAD), showing a reduction in adverse events.
详细描述
Dual antiplatelet therapy consisting in aspirin and clopidogrel is the cornerstone of the treatment of the prevention of the thrombotic events in patients with coronary artery disease (CAD), showing a reduction in adverse events . However, there is a considerable number of patients who continue to have recurrent ischemic events despite this regimen . In fact, in the last years several clinical factors have been associated with impaired clopidogrel-induced effects. Moreover, these clinical factors are strongly related with the presence of high on-treatment platelet reactivity (HPR), which is also associated with the occurrence of adverse thrombotic events, including stent thrombosis, despite correct treatment compliance. Diabetes mellitus, acute coronary syndromes, obesity or chronic kidney disease (CKD) are common examples . This observation encourages the search for new more potent antiplatelet therapies. A new P2Y12 receptor antagonist, ticagrelor, has been approved for clinical use . Ticagrelor is a new non-thienopyridine, a cyclopentyltriazolo-pyrimidine (CPTP), direct acting reversible P2Y12 antagonist. This compound has a more favorable pharmacokinetic (PK) and pharmacodynamics (PD) profile than clopidogrel , which has translated into better clinical outcomes in patients with acute coronary syndrome (ACS) in a recent large, international clinical trial . Interestingly, ticagrelor has showed an impressive clinical benefit in patients with CKD in comparison with those patients without renal impairment .
CKD is highly associated with an increased risk of atherothrombotic events, including stent thrombosis, in patients with CAD . PD studies have shown that patients with impaired renal function are characterized by reduced clopidogrel-induced antiplatelet effects and higher rates of HPR compared with patients with preserved renal function.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients presenting with moderate-high risk non-STEACS defined according the current guidelines
- •Patients received a loading dose or under chronic treatment with aspirin (100 mg per day) as per standard of care
- •Age between 18 and 80 years old
- •BMI between 18 and 35 kg/m2
- •Provide written informed consent prior to any study specific procedures
排除标准
- •History of hemorrhagic stroke or intracranial bleeding
- •Known allergies to aspirin, ticagrelor, or clopidogrel
- •On treatment with oral anticoagulation (Coumarin derivate, dabigatran, rivaroxaban, apixaban)
- •Hemoglobin <10 gm/dL
- •Platelet count <80x106/mL
- •Blood dyscrasias, active bleeding or hemodynamic instability.
- •Patients on hemodialysis or peritoneal dialysis, a change in estimated glomerular filtration rate (eGFR) greater than 15 mL/min within 90 days prior to enrollment, or estimated glomerular filtration rate (eGFR) lower than 15 mL/min/1.73m2
- •Patients with known infectious diseases or neoplasia
- •Baseline ALT >2.5 times the upper limit of normal
- •Patients with sick sinus syndrome (SSS) or high degree AV block without pacemaker protection
- •Drugs interfering with 2C19 metabolism (to avoid interaction with clopidogrel): fluconazole (Diflucan), ketoconazole (Nizoral), voriconazole (VFEND), etravirine (Intelence), felbamate (Felbatol), fluoxetine (Prozac, Serafem, Symbyax), fluvoxamine (Luvox), and ticlopidine (Ticlid). Since omeprazole is the most used proton-pump inhibitor in our clinical environment, we will keep the same prescription rate in both groups to avoid differences results from this described interaction
- •Drugs interfering CYP3A4 metabolism (to avoid interaction with Ticagrelor): Ketoconazole, itraconazole, voriconazole, clarithromycin, nefazodone, ritonavir saquinavir, nelfinavir, indinavir, atazanavir, and telithromizycin
- •Pregnant females
结局指标
主要结局
platelet reactivity units
时间窗: 7+2 days of treatment
The primary endpoint is the comparison of the platelet reactivity units (PRU) values determined by VerfifyNow-P2Y12 system between normal renal function and CKD patients after 7±2 days of concomitant treatment with ticagrelor.
次要结局
- ticagrelor active metabolite levels(30 min, 1, 2, 4 and 6 hours)
- platelet reactivity profiles after 180 mg loading dose to ticagrelor usin MEA(30 min, 1, 2, 4 and 6 hours)
- platelet reactivity profiles after loading dose of ticagrelor(30 min, 1, 2, 4 and 6 hours)