Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois 60611, USA; email:
Annu Rev Pharmacol Toxicol. 2019 Jan 6;59:577-603. doi: 10.1146/annurev-pharmtox-010818-021154. Epub 2018 Oct 8.
Race and ancestry have long been associated with differential risk and outcomes to disease as well as responses to medications. These differences in drug response are multifactorial with some portion associated with genomic variation. The field of pharmacogenomics aims to predict drug response in patients prior to medication administration and to uncover the biological underpinnings of drug response. The field of human genetics has long recognized that genetic variation differs in frequency between ancestral populations, with some single nucleotide polymorphisms found solely in one population. Thus far, most pharmacogenomic studies have focused on individuals of European and East Asian ancestry, resulting in a substantial disparity in the clinical utility of genetic prediction for drug response in US minority populations. In this review, we discuss the genetic factors that underlie variability to drug response and known pharmacogenomic associations and how these differ between populations, with an emphasis on the current knowledge in cardiovascular pharmacogenomics.
种族和祖先一直与疾病的风险和结果以及对药物的反应有关。这些药物反应的差异是多因素的,其中一部分与基因组变异有关。药物基因组学领域旨在预测患者在给药前的药物反应,并揭示药物反应的生物学基础。人类遗传学领域早就认识到,遗传变异在祖先群体中的频率不同,一些单核苷酸多态性仅存在于一个群体中。到目前为止,大多数药物基因组学研究都集中在欧洲和东亚血统的个体上,这导致了在美国少数民族人群中,药物反应的遗传预测的临床实用性存在很大差异。在这篇综述中,我们讨论了药物反应变异性的遗传因素以及已知的药物基因组关联,以及这些关联在不同人群中的差异,重点是心血管药物基因组学的现有知识。