药物基因组学在肺动脉高血压的管理:当前的前景
James C Coons1,2, Philip E Empey1
1Department of Pharmacy and Therapeutics, University of Pittsburgh School of Pharmacy, Pittsburgh, PA, USA.
Pharmacogenomics and personalized medicine
|July 17, 2023
概括
药物基因组变异影响肺动脉高血压 (PAH) 药物的有效性和安全性. 了解这些遗传联系可以个性化PAH治疗,改善患者的治疗结果并减少不良事件.
科学领域:
- 药物基因组学 药物基因组学
- 心血管医学 心血管医学
- 罕见疾病 罕见疾病
背景情况:
- 肺动脉高血压 (PAH) 是一种严重的疾病,导致右心室衰竭.
- 目前的PAH治疗方法具有可变的疗效,需要经验性剂量.
- 药物遗传学 (PGx) 关联可以解释PAH药物反应的个体间变异性.
研究的目的:
- 审查与PAH药物的剂量和结果相关的药物基因.
- 突出PGx在个性化PAH治疗中的作用.
主要方法:
- 关于肺动脉高血压的药物遗传学研究的文献综述.
- 对PAH治疗药物,如prostinil和bosentan的基因药物关联的分析.
主要成果:
- CYP2C8,CYP2C9,CAMK2D和PFAS与特雷布罗斯尼尔的反应和剂量有关.
- CYP2C9 变种影响了特雷普罗斯尼尔的持续性和森坦诱导的肝损伤.
- GNG2变异与内甲素受体对抗剂的改善临床结果相关.
结论:
- 药物基因组标记提供了对PAH治疗的可变反应的洞察力.
- 使用PGx的个性化医疗方法可以优化PAH患者管理.
- 对PGx的进一步研究可以减少治疗延迟和PAH的不良影响.
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