Zannad F
Department of Cardiology, University Hospital of Nancy, France.
Am J Cardiol. 1993 Jan 21;71(3):34A-39A. doi: 10.1016/0002-9149(93)90243-6.
Secondary aldosteronism has deleterious effects in patients with congestive heart failure (CHF) and can contribute to congestion, ventricular arrhythmias, and sudden death. Mortality is higher in patients with elevated levels of plasma aldosterone. Aldosterone increases as CHF progresses as a result of activation of the renin-angiotensin-aldosterone system (RAAS). This is further amplified by the routine use of diuretics. Angiotensin-converting enzyme (ACE) inhibitors produce a profound and consistent inhibition of angiotensin II production, but they exert only a mild and transient antialdosterone effect. In a number of studies involving ACE inhibitors, plasma aldosterone levels at the end of the trial do not differ significantly from baseline. Spironolactone, a specific aldosterone receptor antagonist, may exert an independent and additive effect to that of ACE inhibitors. Apart from its renal effects, recent evidence suggests that spironolactone may exert direct cardiac and vascular effects inhibiting cardiac collagen hypertrophy and limiting vascular constriction. Combining an ACE inhibitor and spironolactone may achieve a more complete inhibition of the whole RAAS and may produce further clinical benefits. The efficacy and safety of such a combination has not been properly addressed. In the CONSENSUS trial, plasma potassium and creatinine levels were not necessarily adversely affected when enalapril was added to the regimens of patients receiving spironolactone, a condition existing in > 40% of the patients enrolled in this study. One prospective open study and other anecdotal reports suggest that combining spironolactone and ACE inhibitors resulted in clinical improvement without serious side effects in patients who could not tolerate further increases in the ACE inhibitor dose.(ABSTRACT TRUNCATED AT 250 WORDS)
继发性醛固酮增多症对充血性心力衰竭(CHF)患者具有有害影响,可导致充血、室性心律失常和猝死。血浆醛固酮水平升高的患者死亡率更高。随着CHF的进展,由于肾素 - 血管紧张素 - 醛固酮系统(RAAS)的激活,醛固酮水平会升高。利尿剂的常规使用会进一步加剧这种情况。血管紧张素转换酶(ACE)抑制剂可对血管紧张素II的产生产生深刻且持续的抑制作用,但它们仅具有轻微且短暂的抗醛固酮作用。在多项涉及ACE抑制剂的研究中,试验结束时的血浆醛固酮水平与基线相比无显著差异。螺内酯是一种特异性醛固酮受体拮抗剂,可能对ACE抑制剂产生独立且相加的作用。除了其对肾脏的作用外,最近的证据表明螺内酯可能具有直接的心脏和血管作用,可抑制心脏胶原增生并限制血管收缩。联合使用ACE抑制剂和螺内酯可能会更全面地抑制整个RAAS,并可能产生进一步的临床益处。这种联合用药的疗效和安全性尚未得到妥善解决。在CONSENSUS试验中,当在接受螺内酯治疗的患者方案中添加依那普利时,血浆钾和肌酐水平不一定会受到不利影响,该研究中超过40%的患者存在这种情况。一项前瞻性开放研究和其他轶事报告表明,对于无法耐受ACE抑制剂剂量进一步增加的患者,联合使用螺内酯和ACE抑制剂可改善临床症状且无严重副作用。(摘要截取自250字)