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Genetic susceptibility to adverse drug reactions.

机译:药物不良反应的遗传易感性。

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摘要

Adverse drug reactions (ADRs) are a major clinical problem. Genetic factors can determine individual susceptibility to both dose-dependent and dose-independent ADRs. Determinants of susceptibility include kinetic factors, such as gene polymorphisms in cytochrome P450 enzymes, and dynamic factors, such as polymorphisms in drug targets. The relative importance of these factors will depend on the nature of the ADR; however, it is likely that more than one gene will be involved in most instances. In the future, whole genome single nucleotide polymorphism (SNP) profiling might allow an unbiased method of determining genetic predisposing factors for ADRs, but might be limited by the lack of adequate numbers of patient samples. The overall clinical utility of genotyping in preventing ADRs needs to be proven by the use of prospective randomized controlled clinical trials.
机译:药物不良反应(ADR)是主要的临床问题。遗传因素可以决定个体对剂量依赖性和剂量依赖性ADR的敏感性。易感性的决定因素包括动力学因素,例如细胞色素P450酶中的基因多态性,以及动力学因素,例如药物靶标中的多态性。这些因素的相对重要性将取决于ADR的性质;但是,在大多数情况下,可能涉及多个基因。将来,全基因组单核苷酸多态性(SNP)分析可能会为确定ADR的遗传易感因素提供一种无偏见的方法,但可能会因缺乏足够数量的患者样本而受到限制。基因型在预防ADR中的整体临床应用需要通过使用前瞻性随机对照临床试验来证明。

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