Department of Clinical and Experimental Medicine, University of Sassari, Viale S.Pietro 8, 07100 Sassari, Italy.
Mol Diagn Ther. 2013 Aug;17(4):205-19. doi: 10.1007/s40291-013-0035-6.
Heart failure (HF) is a widespread syndrome due to left ventricular dysfunction with high mortality, morbidity and health-care costs. Beta-blockers, together with diuretics and ACE-inhibitors or angiotensin receptor blockers, are a cornerstone of HF therapy, as they reduce mortality and morbidity. Nevertheless, their efficacy varies among patients, and genetics is likely to be one of the modifying factors. In this article, literature on the role of candidate genes on the development of HF, its prognosis and pharmacogenomics of β-blockers in patients with HF is reviewed. The available findings do not support, at the present time, a role for genetic tests in the treatment of HF. More large-scale genome-wide studies with adequate methodology and statistical analysis are required before considering genetic tailoring of HF therapy in patients with systolic HF.
心力衰竭(HF)是一种广泛存在的综合征,由于左心室功能障碍导致高死亡率、高发病率和高医疗成本。β受体阻滞剂与利尿剂、血管紧张素转换酶抑制剂或血管紧张素受体阻滞剂一起,是 HF 治疗的基石,因为它们可以降低死亡率和发病率。然而,它们在患者中的疗效存在差异,遗传可能是其中一个调节因素。本文综述了候选基因在 HF 发展、预后以及 HF 患者β受体阻滞剂药物基因组学中的作用的相关文献。目前,遗传检测在 HF 治疗中的作用尚缺乏支持。在考虑对射血分数降低的 HF 患者进行 HF 治疗的遗传定制之前,需要进行更多具有适当方法学和统计分析的大规模全基因组研究。