药物遗传学与精神病学护理:综述与评论

M. Butler
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引用次数: 18

摘要

个性化或精准医疗正在出现在人类疾病的治疗和管理中,基于每个人的遗传模式和对药物的反应,分为两个领域:1)药物遗传学和2)药物基因组学。药物遗传学是研究DNA结构变异及其对药物代谢、疗效和耐受性影响的学科。DNA保持稳定,不随时间或年龄变化。药物遗传学通常基于细胞色素P450酶系统,主要存在于肝脏中,涉及编码细胞色素P450酶产生的基因6 - 9。对药物的反应取决于每个人代谢药物的能力,大多数药物被这种酶系统分解,这取决于每个人的基因组成。药物基因组学是研究影响基因功能但可以改变或受因素(如环境)影响的DNA和RNA特征10-12。因此,药物遗传学研究的是单个基因及其结构,而药物基因组学研究的是受环境影响的基因功能,两者都可以在包括药物代谢在内的人类疾病中发挥作用。美国联邦药物管理局(FDA)和美国国立卫生研究院(NIH)已经确定药物遗传学和药物基因组学是开发和测试新药及其对治疗人类疾病个体影响的重要关键工具10,13,14。药物反应的个体差异现在被认为是西方化社会中常见的多种药物治疗的主要临床问题。不同种族分布的相关基因多态性通过药物代谢细胞色素P450酶的调节被确定为药物反应变异性的来源。莫图尔斯基(Motulsky)于1957年提出了药物相互作用的概念,以及基因影响下个体分解药物或代谢能力的潜在关系15,16,后来得到了基于基因的药代动力学研究的支持。几年来,人们知道某些麻醉剂和剂量会根据个人的反应、手术过程中麻醉的体征和症状而改变,这表明人与人之间的不同反应可能与他们的遗传模式差异有关。
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Pharmacogenetics and Psychiatric Care: A Review and Commentary
Personalized or precision medicine is emerging in the treatment of human diseases and management based on each individual’s genetic pattern and response to drugs categorized into two areas: 1) pharmacogenetics and 2) pharmacogenomics1–5. Pharmacogenetics is the study of DNA structural variations and impact on drug metabolism, efficacy and tolerability. DNA remains stable and does not change with time or age. Pharmacogenetics is most often based on the cytochrome P450 enzyme system, primarily found in the liver and involves genes coding for the production of cytochrome P450 enzymes6–9. The response to medications depends on each individual’s ability to metabolize drugs with most drugs broken down by this enzyme system dependent on the genetic makeup of each person. Pharmacogenomics is the study of DNA and RNA characteristics impacting gene function but can change or be influenced by factors (e.g., environment)10–12. Hence, pharmacogenetics deals with single genes and their structure while pharmacogenomics relates to gene function influenced by the environment, both can play a role in human disease including drug metabolism. The Federal Drug Administration (FDA) and National Institutes of Health (NIH) have identified pharmacogenetics and pharmacogenomics as important key tools in development and testing of new drugs and their impact in treating individuals with human disease10,13,14. Inter-individual variability in drug response is now recognized as a major clinical problem in westernized societies where polymedication is common. Relevant gene polymorphisms with different racial distributions are identified sources of variability in drug responses by the modulation of drug-metabolizing cytochrome P450 enzymes discussed in this report. The conceptualization of drug interaction and potential relationship to an individual’s ability to break down drugs or metabolism influenced by genetics was raised by Motulsky in 195715,16 and later supported by genetic-based pharmacokinetics research. For several years, it was known that certain anesthetic agents and doses would be altered depending on the individual’s response, signs and symptoms during surgical procedures when anesthesia was administered indicating variable responses from person to person possibly related to differences in their genetic patterns.
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