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Impact of genetic variations on pharmacokinetic and pharmacodynamic properties of medicines and the future of drug therapy

机译:遗传变异对药物药代动力学和药物动力学特性的影响及药物治疗的未来

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Genetic variations between individuals usually leads to differences in the drug response asit could affect both pharmacokinetic and pharmacodynamic processes. An example ofmutation of genes that affect drug targets (pharmacodynamic) is VKORC1 gene that codesfor active sites of the enzyme vitamin K epoxide reductase that is responsible foractivation vitamin K. A famous example of mutation affecting pharmacodynamic propertiesof medicine is the anticancer agent irinotecan. Bone marrow suppression is a well knownside effect for this medicine. In many cases, this adverse drug reaction appears to be verysevere compared to the majority of the individuals, and that is possibly due to a mutation ofa gene called UDP-GT 1A1.Identifying exact genes could be helpful in better targeting ofmedicines in the future, Pharmacogenetic testing and individualized medicine widens thewindow of therapy for better treatment approaches, it helps us to reduce both rate oftoxicity and the dose of the drug, so it saves both lives and economically efficient that iswhy it worth funding by drug authorities in order for improving better and economicallyefficient clinical practice in the future.
机译:个体之间的遗传变异通常导致药物反应的差异,因为可以影响药代动力学和药物动力学过程。影响药物靶标(药物动力学)的基因的蒙蔽局部是vkorc1基因,该基因是酶维生素K环氧化物还原酶的活性位点,其是负责任的维生素K的。影响药物动力学性质的突变的一个名称突变的例子是抗癌剂是伊耳替康的抗癌剂。骨髓抑制是本药的知名效果。在许多情况下,与大多数个体相比,这种不良药物反应似乎是非常的,并且可能是由于叫做UDP-GT 1A1的基因的突变。识别确切的基因在未来更好地瞄准医学素,药物发生测试和个性化药物扩大了治疗的窗口,以获得更好的治疗方法,有助于我们减少对药物的速率和药物剂量的速率,因此它可以节省生命和经济效率,这是为了提高药物当局值得资助,以便提高药物权力和未来的经济学效率良好。

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