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临床儿科学中的药物遗传学:挑战与策略

Pharmacogenetics in clinical pediatrics: challenges and strategies.

作者信息

Van Driest Sara L, McGregor Tracy L

机构信息

Department of Pediatrics, Vanderbilt University, 2200 Children's Way, Nashville, TN 37232, USA ; The Monroe Carell Jr Children's Hospital at Vanderbilt, 8232 DOT, 2200 Children's Way, Nashville, TN 37232, USA.

Department of Pediatrics, Vanderbilt University, 2200 Children's Way, Nashville, TN 37232, USA ; The Monroe Carell Jr Children's Hospital at Vanderbilt, 8232 DOT, 2200 Children's Way, Nashville, TN 37232, USA ; The Center for Human Genetics Research, 519 Light Hall, 2215 Garland Avenue, Nashville, TN 37232-0700, USA.

出版信息

Per Med. 2013 Sep;10(7). doi: 10.2217/pme.13.70.

Abstract

The use of genetic information to guide medication decisions holds great promise to improve therapeutic outcomes through increased efficacy and reduced adverse events. As in many areas of medicine, pediatric research and clinical implementation in pharmacogenetics lag behind corresponding adult discovery and clinical applications. In adults, genotype-guided clinical decision support for medications such as clopidogrel, warfarin and simvastatin are in use in some medical centers. However, research conducted in pediatric populations demonstrates that the models and practices developed in adults may be inaccurate in children, and some applications lack any pediatric research to guide clinical decisions. To account for additional factors introduced by developmental considerations in pediatric populations and provide pediatric patients with maximal benefit from genotype-guided therapy, the field will need to develop and employ creative solutions. In this article, we detail some concerns about research and clinical implementation of pharmacogenetics in pediatrics, and present potential mechanisms for addressing them.

摘要

利用基因信息指导用药决策有望通过提高疗效和减少不良事件来改善治疗效果。与医学的许多领域一样,儿科药物遗传学研究和临床应用落后于相应的成人研究发现和临床应用。在成人中,一些医疗中心已在使用针对氯吡格雷、华法林和辛伐他汀等药物的基因型指导临床决策支持。然而,针对儿科人群的研究表明,成人中开发的模型和做法在儿童中可能不准确,而且一些应用缺乏任何儿科研究来指导临床决策。为了考虑儿科人群发育因素引入的其他因素,并使儿科患者从基因型指导治疗中获得最大益处,该领域将需要开发和采用创造性的解决方案。在本文中,我们详细阐述了对儿科药物遗传学研究和临床应用的一些担忧,并提出了解决这些问题的潜在机制。

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