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The inorganic NItrate and eXercise performance in Heart Failure (iNIX-HF) phase II clinical trial: Rationale and study design.心力衰竭患者无机硝酸盐与运动表现(iNIX-HF)II期临床试验:原理与研究设计
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Angiotensin receptor blockers in heart failure: meta-analysis of randomized controlled trials.血管紧张素受体阻滞剂用于心力衰竭:随机对照试验的荟萃分析
J Am Coll Cardiol. 2002 Feb 6;39(3):463-70. doi: 10.1016/s0735-1097(01)01775-2.
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A randomized trial of the angiotensin-receptor blocker valsartan in chronic heart failure.血管紧张素受体阻滞剂缬沙坦用于慢性心力衰竭的一项随机试验。
N Engl J Med. 2001 Dec 6;345(23):1667-75. doi: 10.1056/NEJMoa010713.
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Angiotensin-converting enzyme inhibition potentiates angiotensin II type 1 receptor effects on renal bradykinin and cGMP.血管紧张素转换酶抑制增强血管紧张素II 1型受体对肾缓激肽和环磷酸鸟苷的作用。
Hypertension. 2001 Aug;38(2):183-6. doi: 10.1161/01.hyp.38.2.183.
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High levels of plasma brain natriuretic peptide and interleukin-6 after optimized treatment for heart failure are independent risk factors for morbidity and mortality in patients with congestive heart failure.心力衰竭优化治疗后血浆脑钠肽和白细胞介素-6水平升高是充血性心力衰竭患者发病和死亡的独立危险因素。
J Am Coll Cardiol. 2000 Nov 1;36(5):1587-93. doi: 10.1016/s0735-1097(00)00912-8.
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Plasma bradykinin levels in human chronic congestive heart failure.人类慢性充血性心力衰竭患者的血浆缓激肽水平
Clin Sci (Lond). 2000 Nov;99(5):461-6.
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Effect of losartan compared with captopril on mortality in patients with symptomatic heart failure: randomised trial--the Losartan Heart Failure Survival Study ELITE II.氯沙坦与卡托普利对有症状心力衰竭患者死亡率影响的比较:随机试验——氯沙坦心力衰竭生存研究(ELITE II)
Lancet. 2000 May 6;355(9215):1582-7. doi: 10.1016/s0140-6736(00)02213-3.
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Long-term ACE-inhibitor therapy in patients with heart failure or left-ventricular dysfunction: a systematic overview of data from individual patients. ACE-Inhibitor Myocardial Infarction Collaborative Group.心力衰竭或左心室功能障碍患者的长期血管紧张素转换酶抑制剂治疗:来自个体患者数据的系统综述。血管紧张素转换酶抑制剂心肌梗死协作组
Lancet. 2000 May 6;355(9215):1575-81. doi: 10.1016/s0140-6736(00)02212-1.
8
Improvement in exercise tolerance and symptoms of congestive heart failure during treatment with candesartan cilexetil. Symptom, Tolerability, Response to Exercise Trial of Candesartan Cilexetil in Heart Failure (STRETCH) Investigators.坎地沙坦酯治疗期间运动耐量及充血性心力衰竭症状的改善。坎地沙坦酯治疗心力衰竭的症状、耐受性、运动反应试验(STRETCH)研究者。
Circulation. 1999 Nov 30;100(22):2224-30. doi: 10.1161/01.cir.100.22.2224.
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Functional effects of endogenous bradykinin in congestive heart failure.
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What is the ideal study design for evaluation of treatment for heart failure? Insights from trials assessing the effect of ACE inhibitors on exercise capacity.
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一项单中心、开放标签、随机、平行组研究,评估血管紧张素II受体拮抗剂与血管紧张素转换酶抑制剂在充血性心力衰竭高血压患者中的差异:血管紧张素II受体拮抗剂在充血性心力衰竭高血压患者中的疗效研究

A Single-Center, Open-Label, Randomized, Parallel-Group Study Assessing the Differences Between an Angiotensin II Receptor Antagonist and an Angiotensin-Converting Enzyme Inhibitor in Hypertensive Patients with Congestive Heart Failure: The Research for Efficacy of Angiotensin II Receptor Antagonist in Hypertensive Patients with Congestive Heart Failure Study.

作者信息

Totsuka Nobuo, Awata Nobuhisa, Takahashi Katsuhito, Yamamura Hisako, Nakamura Junko, Tsuchikane Etsuo, Kobayashi Yoshiki, Nishibe Akira, Terai Kazuo

机构信息

Graduate School of Pharmaceutical Science, Osaka University, Osaka, Japan and.

Department of Medicine, Osaka Medical Center for Cancer and Cardiovascular Diseases, Osaka, Japan.

出版信息

Curr Ther Res Clin Exp. 2003 Feb;64(2):81-94. doi: 10.1016/S0011-393X(03)00020-1.

DOI:10.1016/S0011-393X(03)00020-1
PMID:24944358
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4053004/
Abstract

BACKGROUND

Angiotensin II receptor blockers (ARBs) and angiotensin-converting enzyme inhibitors (ACEIs) have been used to treat congestive heart failure (CHF). According to a MEDLINE search, however, few studies are available on the clinical differences between ARBs and ACEIs in CHF.

OBJECTIVE

To examine the clinical differences between an ARB (candesartan cilexetil) and an ACEI (lisinopril) in the treatment of CHF, we investigated exercise capacity, ventricular function, and neurohormonal levels in hypertensive patients with CHF before and after treatment with these agents.

METHODS

Patients with symptoms of CHF (New York Heart Association functional class II-III and left ventricular ejection fraction [LVEF] ≤45%) complicated by hypertension (systolic blood pressure [BP] ≥140 mm Hg or diastolic BP ≥90 mm Hg) were eligible for this single-center, open-label, randomized, parallel-group study. They were given either the ARB or the ACEI for 24 weeks. A cardiopulmonary exercise test and echocardiography were performed. Clinical findings and cardiac events in addition to the CHF symptoms were investigated. Neurohormonal levels were measured before and after 24 weeks of treatment with the study drug. The primary end point of this study was exercise capacity, which was measured using peak oxygen consumption (VO2).

RESULTS

Forty-two patients with CHF were enrolled and 38 (28 men, 10 women; mean [SD] age, 69.0 [8.2] years) completed the study. None of these patients had definite progression of the CHF symptoms. In the ARB-treated patients, mean (SD) peak VO2 (mL/min/kg) and LVEF (%) increased from 14.1 (2.9) to 15.3 (3.4) and from 34.4 (9.5) to 41.8 (9.5), respectively. In the ACEI group, the peak VO2 did not change, but the LVEF (%) increased from 34.2 (10.2) to 40.4 (13.0). However, the differences between ARB and ACEI were not clarified because of the possibility of a small sample size.

CONCLUSIONS

Although this study was not powered to show differences in efficacy between the ARB and ACEI in this study, our findings suggest that both ARB and ACEI had beneficial effects in hypertensive patients with CHF. Some unidentified differences in hemodynamic characteristics were found between the ARB and the ACEI groups.

摘要

背景

血管紧张素II受体阻滞剂(ARBs)和血管紧张素转换酶抑制剂(ACEIs)已被用于治疗充血性心力衰竭(CHF)。然而,根据MEDLINE检索结果,关于ARBs和ACEIs在CHF治疗中的临床差异的研究较少。

目的

为了研究一种ARB(坎地沙坦酯)和一种ACEI(赖诺普利)在治疗CHF时的临床差异,我们调查了高血压合并CHF患者在接受这些药物治疗前后的运动能力、心室功能和神经激素水平。

方法

有CHF症状(纽约心脏协会心功能II-III级且左心室射血分数[LVEF]≤45%)并伴有高血压(收缩压[BP]≥140 mmHg或舒张压BP≥90 mmHg)的患者符合这项单中心、开放标签、随机、平行组研究的条件。他们被给予ARB或ACEI治疗24周。进行了心肺运动试验和超声心动图检查。除了CHF症状外,还调查了临床发现和心脏事件。在使用研究药物治疗24周前后测量神经激素水平。本研究的主要终点是运动能力,通过峰值耗氧量(VO2)来测量。

结果

42例CHF患者入组,38例(28例男性,10例女性;平均[标准差]年龄,69.0[8.2]岁)完成了研究。这些患者均无CHF症状的明确进展。在接受ARB治疗的患者中,平均(标准差)峰值VO2(mL/min/kg)和LVEF(%)分别从14.1(2.9)增加到15.3(3.4)以及从34.4(9.5)增加到41.8(9.5)。在ACEI组中,峰值VO2没有变化,但LVEF(%)从34.2(10.2)增加到40.4(13.0)。然而,由于样本量可能较小,ARB和ACEI之间的差异未得到明确。

结论

尽管本研究没有足够的能力显示ARB和ACEI在疗效上的差异,但我们的研究结果表明,ARB和ACEI对高血压合并CHF患者均有有益作用。在ARB组和ACEI组之间发现了一些未明确的血流动力学特征差异。