创新链/学科链/研发链/产业链

新药研发前沿动态 / 医药领域趋势进展

基因多态性与药物不良反应发生风险的相关性及其临床证据

Correlation between Gene Polymorphism and Risk of Adverse Drug Reaction and Its Clinical Evidence

  • 摘要: 药物不良反应(ADR)是临床用药中常常出现的难题,不但影响药效,还严重威胁患者的生命安全。随着药物基因组学的快速发展,个体间的基因序列差异与ADR之间的相关性不断被证实,但是缺乏全面的归纳和总结。基于遗传药理学和药物基因组学知识库(PharmGKB)和临床药物遗传学实施联盟(CPIC)、美国食品和药品管理局(FDA)等权威组织发布的药物基因组学相关指南,综述近年来高证据等级的基因多态性在预测和避免ADR中的最新进展和重要意义,以期为基因导向的个体化给药提供参考。

     

    Abstract: Adverse drug reaction (ADR), a big issue in clinical medication, greatly affects drug efficacy and seriously threatens the safety of patients. With the rapid development of pharmacogenomics, the clinical correlation between gene polymorphism and ADR has been continuously confirmed, but there is a lack of comprehensive review. Based on Pharmacogenomics Knowledgebase (PharmGKB), pharmacogenomics-related guidelines published by the Clinical Pharmacogenetics Implementation Consortium (CPIC), the US Food and Drug Administration (FDA) and other authoritative organizations, this paper summarizes the significance and recent advances of gene polymorphism with high level of evidence in predicting and avoiding ADR, in order to provide reference for gene-directed individualized medication.

     

/

返回文章
返回