冠状动脉疾病中的药物基因组生物标志物:叙述性综述
Pamila Dua1, Sandeep Seth1, Bhavana Prasher2
1All India Institute of Medical Sciences, Ansari Nagar, New Delhi, India.
称为单核酸多态的遗传变异对冠状动脉疾病 (CAD) 的药物反应产生影响. 识别这些遗传生物标志物可以预测CAD患者的治疗有效性.
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
- 遗传学 是一个遗传学.
背景情况:
- 冠状动脉疾病 (CAD) 是一个重大的死亡率挑战.
- 药物不响应是CAD治疗中的一个常见问题.
- 药物基因组学提供个性化的治疗策略,通过将基因构成与药物疗效联系起来.
研究的目的:
- 审查研究的单核酸多态 (SNPs) 及其与CAD药物反应的关联.
- 为了确定CAD药物治疗的潜在的药物基因组生物标志物.
主要方法:
- 对104项检查染色体和基因全方位多态度的研究进行了系统审查.
- 在CAD患者中,分析了已识别的多态和药物反应/不反应之间的关联.
- 包括跨不同族裔人口的研究.
主要成果:
- 总共有161种多态性被发现与CAD的药物反应或不反应有关.
- 这些关联在各种种族群体中被观察到.
- 已识别的多态体代表了药物基因组生物标记物的潜在池.
结论:
- 单核酸多态性与冠状动脉疾病中药物反应有显著的关联.
- 这些遗传变异可以作为指导CAD药物治疗的预测生物标志物.
- 药物基因组方法有望改善CAD的治疗结果.
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