Erectile Dysfunction Predicts Cardiovascular Events in High-Risk Patients Receiving Telmisartan, Ramipril, or Both

医学 雷米普利 替米沙坦 危险系数 内科学 心肌梗塞 安慰剂 心脏病学 冲程(发动机) 置信区间 勃起功能障碍 心力衰竭 血压 机械工程 替代医学 病理 工程类
作者
Michael Böhm,Magnus Baumhäkel,Koon Teo,Peter Sleight,Jeffrey L. Probstfield,Peggy Gao,Johannes F.E. Mann,Rafael Dı́az,Gilles R. Dagenais,Garry Jennings,Lisheng Liu,Petr Jánský,Salim Yusuf
出处
期刊:Circulation [Ovid Technologies (Wolters Kluwer)]
卷期号:121 (12): 1439-1446 被引量:178
标识
DOI:10.1161/circulationaha.109.864199
摘要

Although erectile dysfunction (ED) is associated with cardiovascular risk factors and atherosclerosis, it is not known whether the presence of ED is predictive of future events in individuals with cardiovascular disease. We evaluated whether ED is predictive of mortality and cardiovascular outcomes, and because inhibition of the renin-angiotensin system in high-risk patients reduces cardiovascular events, we also tested the effects on ED of randomized treatments with telmisartan, ramipril, and the combination of the 2 drugs (ONTARGET), as well as with telmisartan or placebo in patients who were intolerant of angiotensin-converting enzyme inhibitors (TRANSCEND).In a prespecified substudy, 1549 patients underwent double-blind randomization, with 400 participants assigned to receive ramipril, 395 telmisartan, and 381 the combination thereof (ONTARGET), as well as 171 participants assigned to receive telmisartan and 202 placebo (TRANSCEND). ED was evaluated at baseline, at 2-year follow-up, and at the penultimate visit before closeout. ED was predictive of all-cause death (hazard ratio [HR] 1.84, 95% confidence interval [CI] 1.21 to 2.81, P=0.005) and the composite primary outcome (HR 1.42, 95% CI 1.04 to 1.94, P=0.029), which consisted of cardiovascular death (HR 1.93, 95% CI 1.13 to 3.29, P=0.016), myocardial infarction (HR 2.02, 95% CI 1.13 to 3.58, P=0.017), hospitalization for heart failure (HR 1.2, 95% CI 0.64 to 2.26, P=0.563), and stroke (HR 1.1, 95% CI 0.64 to 1.9, P=0.742). The study medications did not influence the course or development of ED.ED is a potent predictor of all-cause death and the composite of cardiovascular death, myocardial infarction, stroke, and heart failure in men with cardiovascular disease. Trial treatment did not significantly improve or worsen ED.URL: http://www.clinicaltrials.gov. Unique identifier: NCT 00153101.
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