ACE (angiotensin-converting enzyme) inhibitors and PDE5 (phosphodiesterase type 5) inhibitors have each been reported to improve endothelial function in cardiovascular disease patients, but the comparative and combined effects of these two classes have not been studied previously. We sought to characterize the acute effects of ramipril alone, sildenafil alone, or their combination on endothelial function in patients with CHF (chronic heart failure). CHF subjects (n=64) were randomized to receive placebo, 10 mg of ramipril alone, 50 mg of sildenafil alone or a combination of ramipril and sildenafil in a double-blind manner. FMD (flow-mediated dilation) of the brachial artery was determined by high-resolution ultrasound imaging before and at 1, 2 and 4 h after administration of the study drug. Ramipril alone increased FMD at 4 h compared with placebo (+2.3±1.3%, P=0.02). Sildenafil alone increased FMD at 1, 2 and 4 h compared with placebo (+3.9±1.4, +4.6±1.8 and +3.7±1.3% respectively, all P<0.02). Sildenafil in combination with ramipril increased FMD at 1, 2 and 4 h when compared with placebo (+3.5±1.5, +4.5±1.8 and +4.8±1.3% respectively, all P<0.03). Ramipril and sildenafil both acutely improved FMD in patients with CHF, with additive effects evident at 4 h during combination therapy. Therefore further work to characterize chronic effects of combined ACE and PDE5 inhibition on endothelial function are warranted.
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April 2005
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Research Article|
March 22 2005
Inhibition of angiotensin-converting enzyme and phosphodiesterase type 5 improves endothelial function in heart failure
Katarzyna HRYNIEWICZ;
Katarzyna HRYNIEWICZ
*Department of Internal Medicine, Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, CT 06510, U.S.A.
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Clarito DIMAYUGA;
Clarito DIMAYUGA
†Department of Medicine, Columbia University College of Physicians and Surgeons, New York, NY 10032, U.S.A.
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Alhakam HUDAIHED;
Alhakam HUDAIHED
*Department of Internal Medicine, Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, CT 06510, U.S.A.
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Ana Silvia ANDRONE;
Ana Silvia ANDRONE
*Department of Internal Medicine, Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, CT 06510, U.S.A.
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Haoyi ZHENG;
Haoyi ZHENG
*Department of Internal Medicine, Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, CT 06510, U.S.A.
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Krzysztof JANKOWSKI;
Krzysztof JANKOWSKI
‡Department of Internal Medicine and Cardiology, Warsaw University, Warsaw, Poland
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Stuart D. KATZ
*Department of Internal Medicine, Section of Cardiovascular Medicine, Yale University School of Medicine, New Haven, CT 06510, U.S.A.
Correspondence: Dr Stuart D. Katz (email [email protected]).
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Publisher: Portland Press Ltd
Received:
September 02 2004
Revision Received:
November 23 2004
Accepted:
December 02 2004
Accepted Manuscript online:
December 02 2004
Online ISSN: 1470-8736
Print ISSN: 0143-5221
The Biochemical Society
2005
Clin Sci (Lond) (2005) 108 (4): 331–338.
Article history
Received:
September 02 2004
Revision Received:
November 23 2004
Accepted:
December 02 2004
Accepted Manuscript online:
December 02 2004
Citation
Katarzyna HRYNIEWICZ, Clarito DIMAYUGA, Alhakam HUDAIHED, Ana Silvia ANDRONE, Haoyi ZHENG, Krzysztof JANKOWSKI, Stuart D. KATZ; Inhibition of angiotensin-converting enzyme and phosphodiesterase type 5 improves endothelial function in heart failure. Clin Sci (Lond) 1 April 2005; 108 (4): 331–338. doi: https://doi.org/10.1042/CS20040266
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