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New advances in beta-blocker therapy in heart failure

机译:β受体阻滞剂治疗心力衰竭的新进展

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摘要

The use of β-blockers (BB) in heart failure (HF) has been considered a contradiction for many years. Considering HF simply as a state of inadequate systolic function, BB were contraindicated because of their negative effects on myocardial contractility. Nevertheless, evidence collected in the past years have suggested that additional mechanisms, such as compensatory neuro-humoral hyperactivation or inflammation, could participate in the pathogenesis of this complex disease. Indeed, chronic activation of the sympathetic nervous system, although initially compensating the reduced cardiac output from the failing heart, increases myocardial oxygen demand, ischemia and oxidative stress; moreover, high catecholamine levels induce peripheral vasoconstriction and increase both cardiac pre- and after-load, thus determining additional stress to the cardiac muscle (1). As a consequence of such a different view of the pathogenic mechanisms of HF, the efficacy of BB in the treatment of HF has been investigated in numerous clinical trials. Results from these trials highlighted BB as valid therapeutic tools in HF, providing rational basis for their inclusion in many HF treatment guidelines. However, controversy still exists about their use, in particular with regards to the selection of specific molecules, since BB differ in terms of adrenergic β-receptors selectivity, adjunctive effects on α-receptors, and effects on reactive oxygen species and inflammatory cytokines production. Further concerns about the heterogeneity in the response to BB, as well as the use in specific patients, are matter of debate among clinicians. In this review, we will recapitulate the pharmacological properties and the classification of BB, and the alteration of the adrenergic system occurring during HF that provide a rationale for their use; we will also focus on the possible molecular mechanisms, such as genetic polymorphisms, underlying the different efficacy of molecules belonging to this class.
机译:在心力衰竭(HF)中使用β受体阻滞剂(BB)多年来一直被认为是矛盾的。单纯将HF视为收缩功能不足的一种状态,因此BB是禁忌的,因为它们对心肌的收缩性具有负面影响。但是,过去几年收集的证据表明,其他机制,例如代偿性神经体液过度激活或炎症,可能参与了这种复杂疾病的发病机制。确实,交感神经系统的慢性激活虽然最初可以补偿衰竭心脏的心输出量减少,但会增加心肌的需氧量,局部缺血和氧化应激。此外,高儿茶酚胺水平会引起周围血管收缩,并增加心脏前后负荷,从而确定了对心肌的额外压力(1)。由于对HF的致病机理有不同的看法,因此在许多临床试验中已经研究了BB在治疗HF中的功效。这些试验的结果突出了BB是HF的有效治疗工具,为将其纳入许多HF治疗指南提供了合理的基础。然而,由于BB在肾上腺素能β-受体选择性,对α-受体的辅助作用以及对活性氧和炎性细胞因子产生的影响方面有所不同,因此关于它们的使用仍存在争议,特别是在选择特定分子方面。有关对BB反应的异质性以及在特定患者中的使用的进一步关注,是临床医生争论的问题。在这篇综述中,我们将概述BB的药理特性和分类,以及在HF期间发生的肾上腺素系统的变化,为其使用提供理论依据;我们还将关注可能的分子机制,例如遗传多态性,这些机制可能是属于此类分子的不同功效的基础。

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