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DOI 10.1097/01.mnh.0000174397.59100.89

Медицинская библиотека · Current opinion in nephrology and hypertension · 2005

Antihypertensive, cardiovascular, and pleiotropic effects of angiotensin-receptor blockers.

Sierra Cristina, de la Sierra Alejandro

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Аннотация

PURPOSE OF REVIEW: To review the antihypertensive, cardiovascular and pleiotropic effects of angiotensin-receptor blockers (ARBs).

RECENT FINDINGS: ARBs are the most recently approved class of antihypertensive agents. They selectively block the angiotensin II type 1 receptor, thus inhibiting most of the deleterious effects of angiotensin II. In addition to blood-pressure control, other benefits may be gained using ARBs. This is because the renin-angiotensin system plays a crucial role in circulatory homoeostasis, and in patients with atherosclerosis, diabetes or hypertension, angiotensin II contributes to the pathophysiology of disease. Evidence-based medicine includes well-controlled studies with mortality and morbidity endpoints in patients with a variety of conditions including hypertension, type 2 diabetes, stroke, renal disease, heart failure, left-ventricular hypertrophy and coronary heart diseases. In addition to these hard endpoints, it has been shown that treatment with ARBs prevents the development of type 2 diabetes, ameliorates coronary and peripheral vascular endothelial dysfunction and decreases plasma levels of several markers of vascular inflammation.

SUMMARY: ARBs are first-line agents for the treatment of hypertension and cardiovascular diseases. Blocking the renin-angiotensin system with these agents has special advantages due to specific vascular and antiatherosclerotic effects, which contribute to a better cardiovascular and renal protection in patients at risk from or with cardiovascular disease.

Для цитирования: Sierra Cristina, de la Sierra Alejandro. Antihypertensive, cardiovascular, and pleiotropic effects of angiotensin-receptor blockers.. Current opinion in nephrology and hypertension. 2005. DOI: 10.1097/01.mnh.0000174397.59100.89.

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