Pharmacogenomics: The Scientific Basis of Rational Drug Development and Prescribing

S. Abraham, H. Jethwa
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引用次数: 1

Abstract

“It is more important to know what sort of a patient has a disease than what sort of a disease a patient has” (Hippocrates 460 BC-370 BC). The holy grail of drug discovery is to ensure that an individual responds positively to an investigational drug with minimal or no adverse events. This could then translate to newly discovered drugs being licenced for prescribing as safe and effective therapeutics. Pharmacogenomics may herald the technology for this aspiration to become reality. Uniting the disciplines of pharmacology and genomics, pharmacogenomics provides a mechanism to understand and predict the response of an individual to a drug or group of drugs. This is based on the premise that an individual’s genotype affects the pharmacokinetics, pharmacodynamics and, ultimately, the individual’s their response to a drug. This review will begin by reviewing the history of drug development and then proceed to discuss the use of pharmacogenomics in drug development through case studies in oncology, respiratory and vaccinology. It will then go on to discuss how pharmacogenomics presently influences prescribing practices and how this technology may have the potential to enhance patient safety when medicines are administered.
药物基因组学:合理药物开发和处方的科学依据
“了解什么样的病人得了什么样的病比了解病人得了什么样的病更重要”(希波克拉底公元前460 -公元前370)。药物发现的终极目标是确保个体对研究药物产生积极反应,而不良事件最少或没有。然后,这可能会转化为新发现的药物,作为安全有效的治疗药物被许可开处方。药物基因组学可能预示着这一愿望成为现实的技术。结合药理学和基因组学的学科,药物基因组学提供了一种机制来理解和预测个体对一种药物或一组药物的反应。这是基于一个前提,即个体的基因型影响药代动力学、药效学,并最终影响个体对药物的反应。本综述将首先回顾药物开发的历史,然后通过肿瘤学、呼吸学和疫苗学的案例研究讨论药物基因组学在药物开发中的应用。然后,它将继续讨论药物基因组学目前如何影响处方实践,以及这项技术如何有可能在给药时提高患者的安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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