Department of Pharmaceutical Sciences, College of Pharmacy, University of South Florida, 12901 Bruce B. Downs Blvd., MDC 30, Tampa, FL, 33612, USA.
Drugs. 2015 Apr;75(6):589-631. doi: 10.1007/s40265-015-0375-0.
Adverse drug reactions (ADRs) are a major public health concern and cause significant patient morbidity and mortality. Pharmacogenomics is the study of how genetic polymorphisms affect an individual's response to pharmacotherapy at the level of a whole genome. This article updates our knowledge on how genetic polymorphisms of important genes alter the risk of ADR occurrence after an extensive literature search. To date, at least 244 pharmacogenes identified have been associated with ADRs of 176 clinically used drugs based on PharmGKB. At least 28 genes associated with the risk of ADRs have been listed by the Food and Drug Administration as pharmacogenomic biomarkers. With the availability of affordable and reliable testing tools, pharmacogenomics looks promising to predict, reduce, and minimize ADRs in selected populations.
药物不良反应(ADRs)是一个主要的公共卫生关注点,会导致患者发病率和死亡率显著增加。药物基因组学是研究遗传多态性如何影响个体对整个基因组水平的药物治疗的反应。本文通过广泛的文献检索,更新了我们对重要基因的遗传多态性如何改变 ADR 发生风险的认识。迄今为止,根据 PharmGKB,至少有 244 个药物基因与 176 种临床使用药物的 ADR 相关。美国食品和药物管理局(FDA)已将至少 28 个与 ADR 风险相关的基因列为药物基因组学生物标志物。随着价格合理且可靠的检测工具的出现,药物基因组学有望在选定人群中预测、减少和最小化 ADR。