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心力衰竭中的药物遗传学:内皮和神经体液功能的基因组标志物

Pharmacogenetics in heart failure: genomic markers of endothelial and neurohumoral function.

作者信息

McNamara Dennis M

机构信息

Heart Failure/Transplantation Program, Genetics Core Laboratory, University of Pittsburgh Medical Center, S-558 Lothrop Street, Pittsburgh, PA 15213, USA.

出版信息

Congest Heart Fail. 2004 Nov-Dec;10(6):302-8. doi: 10.1111/j.1527-5299.2004.03855.x.

Abstract

There is a high potential for pharmacogenetic interaction in the management of many diseases including heart failure. Although genetic tailoring of therapy is not yet a common medical practice, it is foreseeable that some forms of genetic targeting will become standard care by the end of the current decade. This review will summary how genetic variation in two genes involved in both endothelial function and heart failure pathogenesis, angiotensin-converting enzyme and endothelial nitric oxide synthase, influence both heart failure outcomes and the effects of standard therapies.

摘要

在包括心力衰竭在内的许多疾病的治疗中,药物遗传学相互作用具有很高的可能性。尽管根据基因定制治疗尚未成为一种常见的医疗实践,但可以预见,到本十年末,某些形式的基因靶向治疗将成为标准治疗方法。本综述将总结参与内皮功能和心力衰竭发病机制的两个基因——血管紧张素转换酶和内皮型一氧化氮合酶——的基因变异如何影响心力衰竭的预后以及标准治疗的效果。

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