Department of Biotechnology and Genetic Engineering, Jordan University of Science and Technology, Irbid, Jordan.
Rev Med Virol. 2021 Jul;31(4):e2194. doi: 10.1002/rmv.2194. Epub 2020 Nov 17.
The ongoing outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) represents a significant challenge to international health. Pharmacogenomics aims to identify the different genetic variations that exist between individuals and populations in order to determine appropriate treatment protocols to enhance the efficacy of drugs and reduce their side-effects. This literature review provides an overview of recent studies of genetic polymorphisms in genes that mediate the SARS-CoV-2 infection mechanism (ACE1, ACE2, TMPRSS2 and CD26). In addition, genetic variations in the drug-metabolising enzyme genes of several selected drugs used in the treatment of COVID-19 are summarised. This may help construct an effective health protocol based on genetic biomarkers to optimise response to treatment. Potentially, pharmacogenomics could contribute to the development of effective high-throughput assays to improve patient evaluation, but their use will also create ethical, medical, regulatory, and legal issues, which should now be considered in the era of personalised medicine.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的持续爆发对国际健康构成了重大挑战。药物基因组学旨在确定个体和人群之间存在的不同遗传变异,以确定适当的治疗方案,提高药物的疗效并降低其副作用。本文综述了最近关于介导 SARS-CoV-2 感染机制的基因(ACE1、ACE2、TMPRSS2 和 CD26)中遗传多态性的研究。此外,还总结了几种用于治疗 COVID-19 的选定药物的药物代谢酶基因中的遗传变异。这有助于根据遗传生物标志物构建有效的健康方案,以优化对治疗的反应。药物基因组学有可能有助于开发有效的高通量检测方法来改善对患者的评估,但它们的使用也将带来伦理、医疗、监管和法律问题,在个性化医疗时代,这些问题现在应该得到考虑。