Rieder Michael J, Carleton Bruce
CIHR-GSK Chair in Paediatric Clinical Pharmacology, Schulich School of Medicine & Dentistry, Robart Research Institute, Western University London, ON, Canada.
Pharmaceutical Outcomes Programme, Department of Pediatrics, University of British Columbia, BC Children's Hospital Vancouver, BC, Canada.
Front Genet. 2014 Apr 16;5:78. doi: 10.3389/fgene.2014.00078. eCollection 2014.
Adverse drug reactions are a common and important complication of drug therapy in children. Over the past decade it has become increasingly apparent that genetically controlled variations in drug disposition and response are important determinants of adverse events for many important adverse events associated with drug therapy in children. While this research has been difficult to conduct over the past decade technical and ethical evolution has greatly facilitated the ability of investigators to conduct pharmacogenomic studies in children. Some of this research has already resulted in changes in public policy and clinical practice, for example in the case of codeine use by mothers and children. It is likely that the use of pharmacogenomics to enhance drug safety will first be realized among selected groups of children with high rates of drug use such as children with cancer, but it also likely that this research will be extended to other groups of children who have high rates of drug utilization and as well as providing insights into the mechanisms and pathophysiology of adverse drug reactions in children.
药物不良反应是儿童药物治疗中常见且重要的并发症。在过去十年中,越来越明显的是,药物处置和反应方面的基因控制变异是儿童药物治疗相关许多重要不良事件的重要决定因素。虽然在过去十年中进行这项研究很困难,但技术和伦理的发展极大地促进了研究人员在儿童中开展药物基因组学研究的能力。其中一些研究已经导致公共政策和临床实践的改变,例如母亲和儿童使用可待因的情况。利用药物基因组学提高药物安全性可能首先会在用药率高的特定儿童群体中实现,如癌症患儿,但这项研究也可能会扩展到其他药物利用率高的儿童群体,同时也能深入了解儿童药物不良反应的机制和病理生理学。