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首页> 外文期刊>Canadian pharmacists journal: CPJ = Revue des pharmaciens du Canada : RPC >Professional opportunity for pharmacists to integrate pharmacogenomics in medication therapy
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Professional opportunity for pharmacists to integrate pharmacogenomics in medication therapy

机译:药剂师的专业机会,将药物替补中毒纳入药物治疗

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Over the past decade, the integration of genetic information into the daily care of patients has led to a redefined concept of individualized medicine and has made significant progress. Pharmacogenomics (PGx) is becoming one of the pillars of proactive health care and represents the "low-hanging fruit" in the emerging field of genomic medicine, given its potential in predicting medication safety and efficacy. PGx is the study of how variations in an individual's genetic makeup affect the response to medications. Genetic variants may affect the pharmacokinetics as well as the pharmacody-namics of a medication. For example, genetic variations in the cytochrome P-450 (CYP) iso-enzymes can produce differences in enzyme activity that change the amount of drug available in the body. This can have a clinical significance regarding adverse drug reactions, drug efficacy and dose requirements for commonly used drugs, such as antidepressants, opiates, proton pump inhibitors and many more. For instance, clopidogrel is a prodrug that is metabolically converted by the CYP2C19 gene in the liver to its active metabolite and irreversibly inhibits platelet aggregation. Individuals who have significantly reduced function of the CYP2C19 gene may not respond to clopidogrel therapy because of diminished platelet response and may benefit from alternative antiplatelet therapy such as prasugrel or ticagrelor.
机译:在过去十年中,遗传信息将遗传信息与患者日常护理的整合导致了个性化药物的重新定义概念,取得了重大进展。药物替昔甙(PGX)正在成为主动保健的支柱之一,并代表了基因组医学的新兴领域中的“低悬垂的水果”,鉴于预测药物安全性和疗效。 PGX是研究个体遗传构成的变化如何影响对药物的反应。遗传变异可能影响药代动力学以及药物的药理学。例如,细胞色素P-450(CYP)异酶的遗传变异可以产生酶活性的差异,其改变体内可获得的药物量的酶活性。这可以对常用药物的不良药物反应,药物功效和剂量要求等临床意义,例如抗抑郁药,阿片类药物,质子泵抑制剂等等。例如,氯吡格雷是由肝脏中的CYP2C19基因代谢地转化为其活性代谢物的前药,并且不可逆地抑制血小板聚集。由于血小板反应减少,并且可以从血小板反应减少,并且可以从替代抗血小板疗法(如普拉)或TiCagreloLoR等替代抗血小板治疗中受益,而具有显着降低的Cyp2C19基因功能的个体可能不会响应氯吡格雷治疗。

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