ABCG2 基因多态可能影响受阿皮克萨班和里瓦罗克萨班治疗的患者的出血风险
Hamin Kim1, Tae-Jin Song2, Jeong Yee1
1College of Pharmacy and Graduate School of Pharmaceutical Sciences, Ewha Womans University, Seoul, Korea.
在ABCG2和ABCB1中的遗传变异,以及血流和质子抑制剂使用史,与服用阿皮克萨班或里瓦罗克萨班的患者的出血风险有关.
科学领域:
- 药物基因组学 药物基因组学
- 心脏病学 心脏病学
- 在瘤学瘤学.
背景情况:
- 直接口服抗凝剂 (DOAC) 对于预防心房动中风至关重要.
- 流血并发症仍然是DOAC治疗的一个重要问题.
- ABCG2 载体影响了阿皮克萨班和里瓦罗克萨班的药理动力学.
研究的目的:
- 为了研究ABCG2基因变异与治疗阿皮克萨班或里瓦罗克萨班的患者的出血并发症之间的联系.
- 确定导致出血风险的遗传和临床因素.
主要方法:
- 一项涉及293名用阿皮克萨班或里瓦罗克萨班治疗的患者的病例控制研究.
- 对ABCG2和其他相关基因 (ABCB1,CYP3A4,CYP3A5) 中16个单核酸多态的分析.
- 多变量分析以确定出血事件的独立预测因素.
主要成果:
- ABCG2 rs3114018和ABCB1 rs1045642显著与增加出血风险相关.
- 出血史和同时使用质子抑制剂 (PPI) 也被确定为危险因素.
- 修改后的HAS-BLED得分显示出出血并发症的显著预测价值.
结论:
- 除了临床因素,ABCG2 rs3114018和ABCB1 rs1045642与治疗阿皮克萨班/里瓦罗克萨班的患者的出血风险有关.
- 这些发现支持开发个性化治疗策略.
- 整合遗传信息可以优化DOAC治疗,减少出血事件.
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