Pharmacogenomics: current status and future perspectives

被引:74
|
作者
Pirmohamed, Munir [1 ,2 ]
机构
[1] Univ Liverpool, Inst Syst Mol & Integrat Biol, Fac Hlth & Life Sci, Wolfson Ctr Personalized Med, Liverpool, England
[2] Univ Liverpool, Inst Syst Mol & Integrat Biol, Fac Hlth & Life Sci, Ctr Drug Safety Sci, Liverpool, England
基金
英国工程与自然科学研究理事会; 英国医学研究理事会;
关键词
GENOME-WIDE ASSOCIATION; ADVERSE DRUG-REACTIONS; INDUCED LIVER-INJURY; GENETIC-VARIANTS; HYPERSENSITIVITY REACTIONS; ACTIVATING MUTATIONS; COST-EFFECTIVENESS; CLASS-I; IMPLEMENTATION; GENOTYPE;
D O I
10.1038/s41576-022-00572-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In this Review, Munir Pirmohamed provides an overview of the current state of the pharmacogenomics field, using examples of clinically relevant drug-gene associations, before outlining the steps needed for implementation of pharmacogenomics into clinical practice. The role of pharmacogenomics in drug discovery and development is also considered. Inter-individual variability in drug response, be it efficacy or safety, is common and likely to become an increasing problem globally given the growing elderly population requiring treatment. Reasons for this inter-individual variability include genomic factors, an area of study called pharmacogenomics. With genotyping technologies now widely available and decreasing in cost, implementing pharmacogenomics into clinical practice - widely regarded as one of the initial steps in mainstreaming genomic medicine - is currently a focus in many countries worldwide. However, major challenges of implementation lie at the point of delivery into health-care systems, including the modification of current clinical pathways coupled with a massive knowledge gap in pharmacogenomics in the health-care workforce. Pharmacogenomics can also be used in a broader sense for drug discovery and development, with increasing evidence suggesting that genomically defined targets have an increased success rate during clinical development.
引用
收藏
页码:350 / 362
页数:13
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