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[阿利吉仑肾素抑制作用的优势与局限]

[Advantages and limitations of renin inhibition with aliskiren].

作者信息

Azizi M, Frank M, Steichen O, Blanchard A

机构信息

Faculté de médecine, université Paris Descartes, France.

出版信息

Ann Pharm Fr. 2011 May;69(3):142-50. doi: 10.1016/j.pharma.2011.02.002. Epub 2011 Apr 21.

Abstract

In the current context of renin-angiotensin-aldosterone system (RAAS) blockade, angiotensin (Ang) converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBs), or their combination, have proved to be effective in providing cardiovascular and renal protection. However, renin inhibition has long been recognized as the preferred site for blockade of the RAAS because renin represents the first, highly-regulated and rate-limiting step of the system. Up to now, the first orally active renin inhibitors initially tested in humans did not meet the necessary all the criteria (specificity, potency, and pharmacokinetic profile) to become clinically useful drugs. The synthesis of aliskiren, a potent alkane carboxamide renin inhibitor, now provides an orally active compound which, according to its pharmacological profile in normotensive subjects and in patients with hypertension, diabetic nephropathy or heart failure suggests that this drug may be of value for the treatment of patients with cardiovascular and renal disorders. However, long-term studies are needed to demonstrate the efficacy of aliskiren in these clinical settings. The results of the Aliskiren Trial in Type 2 Diabetes Using Cardiorenal Disease Endpoints (ALTITUDE) trial which has already included 8600 patients with type 2 diabetes, proteinuria and a high cardiovascular risk and compared the effects of aliskiren vs. a placebo on a composite endpoint including renal and cardiovascular morbidity and mortality should be provided in 2012.

摘要

在目前肾素-血管紧张素-醛固酮系统(RAAS)阻断的背景下,血管紧张素(Ang)转换酶(ACE)抑制剂和血管紧张素受体阻滞剂(ARBs),或它们的联合使用,已被证明在提供心血管和肾脏保护方面是有效的。然而,长期以来,肾素抑制一直被认为是RAAS阻断的首选部位,因为肾素代表了该系统的第一步,是高度调节且限速的步骤。到目前为止,最初在人体中测试的第一代口服活性肾素抑制剂并未完全满足成为临床有用药物所需的所有标准(特异性、效力和药代动力学特征)。阿利吉仑(一种有效的烷烃羧酰胺类肾素抑制剂)的合成,现在提供了一种口服活性化合物,根据其在血压正常的受试者以及高血压、糖尿病肾病或心力衰竭患者中的药理学特征表明,这种药物可能对治疗心血管和肾脏疾病患者有价值。然而,需要进行长期研究来证明阿利吉仑在这些临床环境中的疗效。阿利吉仑治疗2型糖尿病合并心肾疾病终点试验(ALTITUDE)已经纳入了8600例2型糖尿病、蛋白尿且心血管风险高的患者,比较了阿利吉仑与安慰剂对包括肾脏和心血管发病率及死亡率的复合终点的影响,该试验结果将于2012年公布。

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