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lüll Comparative assessment of angiotensin receptor blockers in different clinical settings Verdecchia P; Angeli F; Repaci S; Mazzotta G; Gentile G; Reboldi GVasc Health Risk Manag 2009[]; 5 (ä): 939-48Cardiovascular and renal disease can be regarded as progressing along a sort of continuum which starts with cardiovascular risk factors (hypertension, diabetes, dyslipidemia, smoking, etc), evolves with progression of atherosclerotic lesions and organ damage, and then becomes clinically manifest with the major clinical syndromes (myocardial infarction, stroke, heart failure, end-stage renal disease). The blood pressure control remains a fundamental mechanism for prevention of cardiovascular disease. The renin-angiotensin system is believed to play an important role along different steps of the cardiovascular disease continuum. Convincing evidence accumulated over the last decade that therapeutic intervention with angiotensin receptor blockers (ARBs) is effective to slow down or block the progression of cardiovascular disease at different steps of the continuum, with measurable clinical benefits. However, despite the shared mechanism of action, each ARB is characterized by specific pharmacological properties that may influence its clinical efficacy. Indeed, important differences among available ARBs emerged from clinical studies. Therefore, generalization of results obtained with a specific ARB to all available ARBs may be misleading. The present review provides a comparative assessment of the different ARBs in their efficacy on major clinical endpoints along the different steps of the cardiovascular disease continuum.|Angiotensin II Type 1 Receptor Blockers/*therapeutic use[MESH]|Antihypertensive Agents/*therapeutic use[MESH]|Blood Pressure/*drug effects[MESH]|Cardiovascular Diseases/*drug therapy/etiology/physiopathology[MESH]|Diabetic Nephropathies/*drug therapy/physiopathology[MESH]|Disease Progression[MESH]|Evidence-Based Medicine[MESH]|Heart Failure/drug therapy/physiopathology[MESH]|Humans[MESH]|Hypertension/complications/*drug therapy/physiopathology[MESH]|Myocardial Infarction/drug therapy/physiopathology[MESH]|Renin-Angiotensin System/*drug effects[MESH]|Treatment Outcome[MESH] |