基因型导向与标准华法林剂量的随机试验,用于开始口服抗凝药的患者
Jeffrey L Anderson1, Benjamin D Horne, Scott M Stevens
1Cardiovascular Department, LDS Hospital, Intermountain Healthcare, Salt Lake City, UT, USA. jeffrey.anderson@intermountainmail.org
Circulation
|November 9, 2007
概括
药物遗传学引导的华法林剂量提高了剂量准确性和效率. 虽然减少范围外国际规范化比率 (INR) 的首要目标未实现,但子集分析显示了特定遗传特征的前景.
科学领域:
- 药物基因组学 药物基因组学
- 临床药理学 临床药理学
- 个性化医疗是个性化的医疗.
背景情况:
- 根据药物遗传学个性化的华法林剂量是一个有希望的方法.
- 有限的随机试验数据存在于药物遗传学引导的华法林剂量.
研究的目的:
- 为了评估与标准剂量相比,药物遗传学引导的华法林剂量的疗效.
- 评估对剂量准确度,效率和国际标准化比率 (INR) 控制的影响.
主要方法:
- 开始服用华法林的206名患者被随机分配到药物遗传学导向或标准剂量.
- 对CYP2C9变体和VKORC1C1173T进行了基因型鉴定.
- 一个结合遗传和临床因素的回归算法指导了干预组的剂量.
主要成果:
- 药物遗传学导向剂量更准确地预测稳定剂量,需要更少和更小的调整.
- 主要终点,即范围外的INR的百分比,在各组之间没有显著差异 (30.7%与33.1%).
- 探索性分析显示,野生类型和多变异基因型子组的INR控制有所改善.
结论:
- 药物遗传学和临床因素引导的华法林剂量算法提高了启动准确性和效率.
- 减少范围外的INRs的主要终点在整个研究人群中没有达到.
- 小组分析表明,在特定遗传特征中,药物遗传指导具有潜在的益处.
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