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心力衰竭中除血管紧张素转换酶抑制剂外的醛固酮拮抗作用。

Aldosterone antagonism in addition to angiotensin-converting enzyme inhibitors in heart failure.

作者信息

Bauersachs J, Fraccarollo D

机构信息

Medizinische Universitätsklinik, Würzburg, Germany.

出版信息

Minerva Cardioangiol. 2003 Apr;51(2):155-64.

Abstract

Although the role of the systemic renin-angiotensin-aldosterone system in the pathophysiology of heart failure is well-known for years, the impact of a local cardiac aldosterone system has been recognized recently. Aldosterone promotes cardiac hypertrophy and fibrosis in hypertension and heart failure and is involved in left ventricular remodeling after myocardial infarction. Plasma aldosterone levels in patients with heart failure are an indicator of a worse prognosis. Although ACE inhibitor therapy in these patients reduces plasma aldosterone levels, this effect is only transitory, a phenomenon referred to as "aldosterone escape". Even maximally recommended doses of ACE inhibitors do not completely prevent ACE-mediated formation of angiotensin II in chronic heart failure, and those patients with increased aldosterone levels during ACE inhibition have impaired exercise capacity. The RALES study has demonstrated convincingly that in patients with heart failure, addition of the mineralocorticoid receptor antagonist spironolactone (25 mg/d) to ACE inhibition markedly reduces mortality and prevents worsening heart failure. While reduction of excessive extracellular matrix turnover leading to decreased fibrosis appears to be the most important effect of spironolactone in heart failure, other mechanisms such as regression of hypertrophy, improvement of endothelial function, enhanced renal sodium excretion and antiarrhythmic actions may contribute. In RALES, low-dose spironolactone did not confer a substantial risk of hyperkalemia, however, with broader use of spironolactone in heart failure, cases of hyperkalemia associated with the use of this drug increase. Close control of serum potassium and creatinine and estimation of creatinine clearance are mandatory, especially in the presence of additional factors impairing renal function. The new and more selective aldosterone antagonist eplerenone which is devoid of some side effects of spironolactone, has been shown to be effective in hypertension and holds great promise as future therapeutic agent in patients with heart failure.

摘要

尽管多年来人们已经熟知全身肾素 - 血管紧张素 - 醛固酮系统在心力衰竭病理生理学中的作用,但局部心脏醛固酮系统的影响直到最近才被认识到。醛固酮在高血压和心力衰竭中促进心脏肥大和纤维化,并参与心肌梗死后的左心室重构。心力衰竭患者的血浆醛固酮水平是预后较差的一个指标。尽管这些患者使用血管紧张素转换酶(ACE)抑制剂治疗可降低血浆醛固酮水平,但这种作用只是暂时的,这一现象被称为“醛固酮逃逸”。即使是最大推荐剂量的ACE抑制剂也不能完全防止慢性心力衰竭中ACE介导的血管紧张素II的形成,并且那些在ACE抑制期间醛固酮水平升高的患者运动能力受损。随机醛固酮评估研究(RALES)令人信服地证明,在心力衰竭患者中,在ACE抑制治疗基础上加用盐皮质激素受体拮抗剂螺内酯(25毫克/天)可显著降低死亡率并预防心力衰竭恶化。虽然减少导致纤维化减少的过度细胞外基质周转似乎是螺内酯在心力衰竭中最重要的作用,但其他机制如肥大消退、内皮功能改善、增强肾钠排泄和抗心律失常作用也可能起作用。在RALES研究中,低剂量螺内酯并未带来高钾血症的实质性风险,然而,随着螺内酯在心力衰竭中的更广泛应用,与使用该药物相关的高钾血症病例有所增加。必须密切监测血清钾和肌酐水平并评估肌酐清除率,尤其是在存在损害肾功能的其他因素时。新型且更具选择性的醛固酮拮抗剂依普利酮没有螺内酯的一些副作用,已被证明在高血压治疗中有效,并有望成为未来心力衰竭患者的治疗药物。

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