药物遗传学
医学
药品
药理学
精密医学
阿托莫西汀
药物基因组学
硫嘌呤甲基转移酶
生物信息学
基因
哌醋甲酯
生物
内科学
基因型
硫唑嘌呤
精神科
遗传学
注意缺陷多动障碍
病理
疾病
作者
Laura B. Ramsey,Jacob T. Brown,Susan I. Vear,Jeffrey R. Bishop,Sara L. Van Driest
标识
DOI:10.1146/annurev-pharmtox-010919-023459
摘要
Pharmacogenetics is a key component of precision medicine. Genetic variation in drug metabolism enzymes can lead to variable exposure to drugs and metabolites, potentially leading to inefficacy and drug toxicity. Although the evidence for pharmacogenetic associations in children is not as extensive as for adults, there are several drugs across diverse therapeutic areas with robust pediatric data indicating important, and relatively common, drug-gene interactions. Guidelines to assist gene-based dose optimization are available for codeine, thiopurine drugs, selective serotonin reuptake inhibitors, atomoxetine, tacrolimus, and voriconazole. For each of these drugs, there is an opportunity to clinically implement precision medicine approaches with children for whom genetic test results are known or are obtained at the time of prescribing. For many more drugs that are commonly used in pediatric patients, additional investigation is needed to determine the genetic factors influencing appropriate dose.
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