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心力衰竭中的心脏不同步性及对心脏再同步治疗的反应:遗传易感性会起作用吗?

Cardiac dyssynchrony and response to cardiac resynchronisation therapy in heart failure: can genetic predisposition play a role?

作者信息

Lahrouchi N, Bezzina C R

机构信息

Department of Experimental Cardiology, Room K2-116, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.

出版信息

Neth Heart J. 2016 Jan;24(1):11-5. doi: 10.1007/s12471-015-0766-6.

Abstract

Cardiac resynchronisation therapy (CRT) is an accepted treatment for heart failure patients with depressed left ventricular (LV) function and dyssynchrony. However, despite better clinical outcome and improved cardiac function after CRT in the majority of eligible heart failure patients, a large proportion of implanted patients do not seem to benefit clinically from this therapy. In this review we consider whether genetic factors may play a role in modulating response to CRT and summarise the few genetic studies that have investigated the role of genetic variation in candidate genes.

摘要

心脏再同步治疗(CRT)是治疗左心室(LV)功能降低且存在不同步的心力衰竭患者的一种公认疗法。然而,尽管大多数符合条件的心力衰竭患者在接受CRT治疗后临床结局更佳且心功能有所改善,但很大一部分植入该疗法的患者似乎并未在临床上从这种治疗中获益。在本综述中,我们探讨遗传因素是否可能在调节对CRT的反应中发挥作用,并总结了少数研究候选基因中遗传变异作用的遗传学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a72/4692826/29f4dc5980ed/12471_2015_766_Fig1_HTML.jpg

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