Macdonald J E, Kennedy N, Struthers A D
Department of Clinical Pharmacology and Therapeutics, Ninewells Hospital and Medical School, Dundee DD19SY, UK.
Heart. 2004 Jul;90(7):765-70. doi: 10.1136/hrt.2003.017368.
To examine whether the favourable effects on endothelial function, vascular angiotensin converting enzyme (ACE) activity, cardiac remodelling, autonomic function, and QT intervals of spironolactone in combination with ACE inhibitor also occur in patients with New York Heart Association class I-II congestive heart failure (CHF) taking optimal treatment (including beta blockers).
Double blind, crossover study comparing 12.5-50 mg/24 hours spironolactone (three months) with placebo in 43 patients with class I-II CHF taking ACE inhibitors and beta blockers.
Acetylcholine induced vasodilatation improved with spironolactone (p = 0.044). Vascular ACE activity fell (p = 0.006). QTc and QTd fell (mean (SD) QTc 473 (43.1) ms with placebo, 455 (35.4) ms with spironolactone, p = 0.002; QTd 84.5 (41.3) ms with placebo, 72.1 (32.3) ms with spironolactone, p = 0.037). beta-Type natriuretic peptide (BNP) and procollagen III N-terminal peptide (PIIINP) concentrations were also reduced by spironolactone (mean (SD) BNP 48.5 (29.6) pg/ml with placebo, 36.8 (28.5) pg/ml with spironolactone, p = 0.039; PIIINP 3.767 (1.157) microg/ml with placebo, 3.156 (1.123) microg/ml with spironolactone, p = 0.000).
Spironolactone improves vascular function (endothelial function, vascular ACE activity) and other markers of prognosis (BNP, collagen markers, and QT interval length) in asymptomatic or mild CHF when added to optimal treatment including beta blockade. This gives support to the hypothesis that the prognostic benefit seen in RALES (randomised aldactone evaluation study) and EPHESUS (eplerenone postacute myocardial infarction heart failure efficacy and survival study) may also occur in patients with milder CHF already taking standard optimal treatment.
探讨螺内酯联合血管紧张素转换酶(ACE)抑制剂对纽约心脏协会I-II级充血性心力衰竭(CHF)且接受最佳治疗(包括β受体阻滞剂)患者的内皮功能、血管ACE活性、心脏重塑、自主神经功能及QT间期是否也有有益作用。
43例I-II级CHF患者在服用ACE抑制剂和β受体阻滞剂的基础上,进行双盲、交叉研究,比较12.5 - 50mg/24小时螺内酯(三个月)与安慰剂的效果。
螺内酯使乙酰胆碱诱导的血管舒张得到改善(p = 0.044)。血管ACE活性下降(p = 0.006)。QTc和QTd下降(均值(标准差):安慰剂组QTc为473(43.1)毫秒,螺内酯组为455(35.4)毫秒,p = 0.002;安慰剂组QTd为84.5(41.3)毫秒,螺内酯组为72.1(32.3)毫秒,p = 0.037)。螺内酯还降低了β型利钠肽(BNP)和前胶原III N端肽(PIIINP)的浓度(均值(标准差):安慰剂组BNP为48.5(29.6)pg/ml,螺内酯组为36.8(28.5)pg/ml,p = 0.039;安慰剂组PIIINP为3.767(1.157)μg/ml,螺内酯组为3.156(1.123)μg/ml,p = 0.000)。
在包括β受体阻滞剂的最佳治疗基础上加用螺内酯,可改善无症状或轻度CHF患者的血管功能(内皮功能、血管ACE活性)及其他预后指标(BNP、胶原指标和QT间期长度)。这支持了以下假设:在RALES(随机螺内酯评估研究)和EPHESUS(依普利酮急性心肌梗死后心力衰竭疗效和生存研究)中观察到的预后益处,在已经接受标准最佳治疗的轻度CHF患者中也可能出现。