首页> 美国卫生研究院文献>European Journal of Heart Failure >Dual angiotensin receptor and neprilysin inhibition as an alternative to angiotensin-converting enzyme inhibition in patients with chronic systolic heart failure: rationale for and design of the Prospective comparison of ARNI with ACEI to Determine Impact on Global Mortality and morbidity in Heart Failure trial (PARADIGM-HF)
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Dual angiotensin receptor and neprilysin inhibition as an alternative to angiotensin-converting enzyme inhibition in patients with chronic systolic heart failure: rationale for and design of the Prospective comparison of ARNI with ACEI to Determine Impact on Global Mortality and morbidity in Heart Failure trial (PARADIGM-HF)

机译:在慢性收缩性心力衰竭患者中双重血管紧张素受体和中性溶酶抑制作用可替代血管紧张素转换酶抑制作用:ARNI与ACEI的前瞻性比较的原理和设计以确定在心衰试验中对全球死亡率和发病率的影响(PARADIGM- HF)

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摘要

AimsAlthough the focus of therapeutic intervention has been on neurohormonal pathways thought to be harmful in heart failure (HF), such as the renin–angiotensin–aldosterone system (RAAS), potentially beneficial counter-regulatory systems are also active in HF. These promote vasodilatation and natriuresis, inhibit abnormal growth, suppress the RAAS and sympathetic nervous system, and augment parasympathetic activity. The best understood of these mediators are the natriuretic peptides which are metabolized by the enzyme neprilysin. LCZ696 belongs to a new class of drugs, the angiotensin receptor neprilysin inhibitors (ARNIs), which both block the RAAS and augment natriuretic peptides.
机译:目的尽管治疗干预的重点一直放在被认为对心力衰竭(HF)有害的神经激素途径上,例如肾素-血管紧张素-醛固酮系统(RAAS),但潜在有益的反调节系统在HF中也很活跃。这些促进血管舒张和利尿,抑制异常生长,抑制RAAS和交感神经系统,并增强副交感神经活动。这些介体中最能理解的是利尿钠肽,其通过中性溶酶进行代谢。 LCZ696属于一类新的药物,即血管紧张素受体中性溶酶抑制剂(ARNIs),它既能阻断RAAS,又能增加利钠肽。

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