Wu Haifeng M, Xu Lihui, Sedmak Daniel D, Marsh Clay B, Wurster Mark W
Per Med. 2010 Jan;7(1):65-73. doi: 10.2217/pme.09.67.
In terms of managing thrombotic disorders, genotype-based individualized patient care emerged as early as 1994 when the association of factor V Leiden (G1691A), and later, prothrombin (G20210A), with thrombotic phenotypes were discovered. Since then, genetic tests for specific thrombophilic SNPs have been routinely incorporated into daily practices in both thrombotic risk assessment and clinical decision-making with respect to prophylactic anti-thrombotic therapy. Recently, the area of pharmacogenomics in major anti-thrombotic drugs, such as warfarin and clopidogrel, has been the principal driver for personalized therapy based on one's own individual characteristics.
在血栓性疾病的管理方面,基于基因型的个体化患者护理早在1994年就已出现,当时发现了凝血因子V莱顿突变(G1691A)以及随后的凝血酶原(G20210A)与血栓形成表型之间的关联。从那时起,针对特定血栓形成倾向单核苷酸多态性(SNP)的基因检测已常规纳入日常实践中的血栓形成风险评估以及预防性抗血栓治疗的临床决策。最近,主要抗血栓药物如华法林和氯吡格雷的药物基因组学领域已成为基于个人特征进行个性化治疗的主要推动因素。