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心力衰竭的基因治疗。

Gene therapy for heart failure.

作者信息

Thompson Richard B, Rungwerth Katrin, Koch Walter J

机构信息

Department of Surgery, Duke University Medical Center, Durham, North Carolina, USA.

出版信息

Ann Med. 2004;36 Suppl 1:106-15. doi: 10.1080/17431380410032652.

Abstract

Despite our continued advances in the management of coronary artery disease, there have been no significant reductions in the morbidity or mortality related to end-stage heart failure. The syndrome of heart failure represents a common endpoint for several disease processes, however, at the molecular level there are certain biochemical similarities common to all failing myocardium. Targeting these derangements with gene therapy represents a promising option in the treatment of heart failure. In this review, we will discuss the common biochemical changes that occur in the failing heart, novel therapeutic targets, including the beta-adrenergic receptor system and intracellular calcium regulation, and the vectors and transfer methodology responsible for delivering these transgenes to the myocardium.

摘要

尽管我们在冠状动脉疾病管理方面不断取得进展,但与终末期心力衰竭相关的发病率和死亡率并未显著降低。心力衰竭综合征是几种疾病过程的常见终点,然而,在分子水平上,所有衰竭心肌都存在某些共同的生化相似性。通过基因治疗针对这些紊乱情况是治疗心力衰竭的一个有前景的选择。在这篇综述中,我们将讨论衰竭心脏中发生的常见生化变化、新的治疗靶点,包括β-肾上腺素能受体系统和细胞内钙调节,以及负责将这些转基因传递到心肌的载体和转移方法。

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