心力衰竭治疗基因剪裁的进展。

John H Lillvis, David E Lanfear
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引用次数: 0

摘要

心力衰竭(HF)是一种现代流行病和异质性疾病,有许多治疗选择。虽然对每种治疗的平均反应是有利的,但对心衰治疗的反应存在显着的个体差异。因此,对于单个患者或亚组患者的最佳方案是难以捉摸的,目前的治疗主要是经验性的。心衰治疗的药物遗传学定制可能为改善心衰治疗提供重要机会。常见的遗传变异存在于与大多数HF药物相关的基因中,其中许多已知的功能后果或与药物反应建立了关系。本文综述了目前对心衰治疗药物的药理学理解,包括血管紧张素转换酶抑制剂和β受体阻滞剂,并重点介绍了该领域的最新进展和中期预期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Progress toward genetic tailoring of heart failure therapy.

Heart failure (HF) is a modern epidemic and a heterogeneous disorder with many therapeutic options. While the average response to each individual treatment is favorable, significant interindividual variation exists in the response to HF therapeutics. As a result, the optimal regimen for an individual patient or subgroup of patients is elusive, with current treatment being mainly empirical. Pharmacogenetic customization of HF therapy may provide an important opportunity to improve the treatment of HF. Common genetic variations exist in genes related to most classes of HF drugs, many of which have known functional consequences for or established relationships with drug response. This review summarizes the current understanding of the pharmacogenetics of HF therapeutics, including angiotensin-converting enzyme inhibitors and beta-blockers, and focuses on recent advances and medium-term expectations for the field.

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Current Opinion in Molecular Therapeutics
Current Opinion in Molecular Therapeutics 医学-生物工程与应用微生物
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