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发育药物遗传学:应用于新生儿药理学和毒理学的一般范式。

Developmental pharmacogenetics: a general paradigm for application to neonatal pharmacology and toxicology.

作者信息

Leeder J S

机构信息

Division of Clinical Pharmacology and Medical Toxicology, Department of Pediatrics, Children's Mercy Hospitals and Clinics and School of Medicine, University of Missouri-Kansas City, Kansas City, Missouri, USA.

出版信息

Clin Pharmacol Ther. 2009 Dec;86(6):678-82. doi: 10.1038/clpt.2009.195. Epub 2009 Oct 28.

Abstract

Therapy in newborn infants presents unique challenges. The consequences of exposure of the fetus to medications and environmental contaminants in utero (following the mother's exposure to these) may present, in the newborn, as congenital malformations or adverse drug reactions or have unknown long-term consequences. Risk is not uniformly distributed across a population. Rather, pharmacogenomic principles assert that an individual's unique clinical, genomic, and environmental information can be used to accurately predict predisposition to risk. The challenge is to identify the specific factors--genetic and nongenetic--that contribute to increased risk.

摘要

新生儿治疗面临着独特的挑战。胎儿在子宫内接触药物和环境污染物(母亲接触这些物质后),其后果在新生儿身上可能表现为先天性畸形或药物不良反应,或者产生未知的长期影响。风险在人群中的分布并不均匀。相反,药物基因组学原理认为,个体独特的临床、基因组和环境信息可用于准确预测风险易感性。挑战在于识别导致风险增加的具体因素——遗传因素和非遗传因素。

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