Endothelial dysfunction: how can one intervene at the beginning of the cardiovascular continuum?

Roland E Schmieder
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引用次数: 42

Abstract

Endothelial dysfunction, characterized by impaired nitric oxide activity, constitutes an early step in the pathogenesis of atherosclerotic disease. Prospective studies have shown that impaired endothelium-dependent vasorelaxation and the vasodilatory response of coronary arteries to acetylcholine predict cardiovascular events. Microalbuminuria and estimated glomerular filtration rate, which are both deeply influenced by renal nitric oxide activity, are predictors of cardiovascular outcome and total mortality but develop at a later stage of renal impairment. Endothelial dysfunction reflects early stage renal involvement in the atherosclerotic processes. The Telmisartan versus Ramipril in renal ENdothelium DYsfunction (TRENDY) trial examined endothelial function of the renal vasculature as a therapeutic target in patients with hypertension and type 2 diabetes, but without albuminuria. The rationale was that blockade of the renin-angiotensin system (RAS) is cardio- and renoprotective at later stages of the disease, but the impact of blockade of the RAS at earlier stages of disease is unknown. The results of TRENDY indicate that the endothelial function, as assessed by basal nitric oxide activity, can be improved after RAS blockade. These data complement the results of the Diabetics Exposed to Telmisartan And enalaprIL (DETAIL) trial, which demonstrated that telmisartan and enalapril similarly decelerate the progression of overt diabetic nephropathy. The results of TRENDY are in accordance with the observed changes in peripheral circulation. Endothelium-dependent vasorelaxation could be improved with angiotensin II receptor blockers, but not with diuretics or beta-blockers, in hypertensive patients. Intervention at the beginning of the renal and cardiovascular continuum offers the opportunity to prevent the fatal development towards renal and cardiac failure.

内皮功能障碍:如何在心血管连续体开始时进行干预?
以一氧化氮活性受损为特征的内皮功能障碍是动脉粥样硬化疾病发病机制的早期步骤。前瞻性研究表明,内皮依赖性血管松弛受损和冠状动脉对乙酰胆碱的血管舒张反应可预测心血管事件。微量白蛋白尿和估计的肾小球滤过率都深受肾脏一氧化氮活性的影响,它们是心血管结局和总死亡率的预测因子,但在肾脏损害的后期才会出现。内皮功能障碍反映了动脉粥样硬化过程中早期肾脏受累。替米沙坦与雷米普利治疗肾内皮功能障碍(赫基)试验检测了肾血管内皮功能作为高血压和2型糖尿病患者的治疗靶点,但没有蛋白尿。其基本原理是,阻断肾素-血管紧张素系统(RAS)在疾病晚期对心脏和肾脏有保护作用,但在疾病早期阻断RAS的影响尚不清楚。新潮的结果表明,以基础一氧化氮活性评估的内皮功能可以在RAS阻断后得到改善。这些数据补充了替米沙坦和依那普利(DETAIL)试验的结果,该试验表明,替米沙坦和依那普利类似地减缓了显性糖尿病肾病的进展。新潮的结果与观察到的外周循环变化一致。血管紧张素受体阻滞剂可以改善高血压患者的内皮依赖性血管松弛,但利尿剂或受体阻滞剂不能改善。在肾脏和心血管连续体的开始进行干预提供了机会,以防止肾和心力衰竭的致命发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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