Circulation Journal Official Journal of the Japanese Circulation Society http://www. j-circ.or.jp atients with acute myocardial infarction (AMI) have a greatly increased risk of subsequent fatal and non-fatal cardiovascular events. Pharmacotherapy is widely accepted to be effective for secondary prevention, but a considerable number of patients still have cardiovascular events. Many randomized, placebo-controlled trials have demonstrated that inhibition of the renin-angiotensin-aldosterone system (RAS) by treatment with an angiotensin-converting enzyme inhibitor (ACEI) reduces the risk of death as well as of major non-fatal cardiovascular events after AMI, and prevents events related to ischemia and atherosclerosis, regardless of blood pressure. 1,2Angiotensin II receptor blockers (ARBs) are thought to act through angiotensin type 1 receptors without affecting the breakdown of bradykinin, thereby avoiding the undesirable side-effects of ACEIs. ARBs may offer thus an alternative approach to RAS inhibition. Recent trials have demonstrated that ARBs are as effective as ACEIs in improving survival and reducing cardiovascular morbidity in patients with congestive heart failure. 3-5 These findings suggest that combined treatment with an ACEI and ARB might more systematically inhibit RAS than ACEI monotherapy. The combined effects of these drugs might thus have higher anti-atherosclerotic efficacy. Whether a combination of these drugs has a favorable effect on coronary atherosclerosis in patients with AMI after successful coronary revascularization, however, remains to be The aim of the present study was to assess the effects of angiotensin II receptor blocker (ARB) on coronary plaque progression in patients with acute myocardial infarction (AMI) who received an angiotensin-converting enzyme inhibitor (ACEI).