Extended Japan Assessment of Pitavastatin and Atorvastatin in Acute Coronary Syndrome

Kyoto University238 enrolled

Overview

The objective of this study is to verify the relationship between coronary plaque regression and cardiovascular prevention in long term follow up of the Japan Assessment of Pitavastatin and Atorvastatin in Acute Coronary Syndrome (JAPAN-ACS) study \[NCT00242944\]. In addition, the effect of serum lipid levels or different type of statins on cardiovascular prevention will also be examined.

Several previous multicenter studies using intravascular ultrasound (IVUS) imaging have revealed that statins attenuate the progression of atherosclerosis or even provide regression of plaque volume. Indeed, the Japan Assessment of Pitavastatin and Atorvastatin in Acute Coronary Syndrome (JAPAN-ACS) trial \[NCT00242944\] has revealed that early aggressive statin therapy in patients with acute coronary syndrome (ACS) significantly reduces the plaque volume of non-culprit coronary lesions On the other hands, a direct relationship between atheroma progression and regression on IVUS and clinical events has not been clearly defined. To verify that relationship, long term follow up of the JAPAN-ACS study will be performed. Clinical outcome of patients with regressed plaque and progressed plaque will be compared. In addition, the objectives of this study are to evaluate the effect of serum lipid levels or different type of statins on cardiovascular prevention.

Study Type

OBSERVATIONAL

Enrollment

238

Conditions

Statin Coronary Plaque Acute Coronary Syndrome Intravascular Ultrasound

Eligibility

Sex: ALLMin age: 20 Years

Medical Language ↔ Plain English

At the enrollment of original study Inclusion Criteria: * Patients with written consent by their own volition after being provided sufficient explanation for their participation in this clinical trial * Patients 20 years or older at the time of their consent * Patients with hypercholesterolemia as defined by any of the following criteria: TC \>= 220 mg/dL; LDL-C \>= 140 mg/dL; Cholesterol-lowering treatment is necessary in accordance with the investigator's judgement when LDL-C \>= 100 mg/dL or TC \>= 180 mg/dL. * Patients who have been diagnosed with acute coronary syndrome * Patients with successful percutaneous coronary intervention (PCI) by intravascular ultrasound (IVUS) guidance * Patients having coronary plaques (\>= 500 µm in thickness or 20% or more in % plaque) at \>= 5 mm from the previously treated area in the same branch of coronary artery Exclusion Criteria: * Patients with bypass graft or in-stent restenosis at the site of PCI * Patients who had received PCI on the lesion in the past where the evaluation of coronary plaque volume is planned * Patients who had plaques in a non-culprit site and might receive PCI during the treatment period * Patients receiving lipid-lowering drugs (statins, fibrates, probucol, nicotinic acid or cholesterol absorption inhibitors) * Patients with familial hypercholesterolemia * Patients with cardiogenic shock * Patients receiving cyclosporine * Patients with any allergy to pitavastatin or atorvastatin * Patients with hepatobiliary disorders * Pregnant women, women suspected of being pregnant, or lactating women * Patients with renal disorders or undergoing dialysis * Patients who are ineligible in the opinion of the investigator

Outcomes

Primary Outcomes

Composite endpoint

Occurrence of one of following events: Cardiovascular death (death from cardiac cause or stroke or peripheral artery disease) Non-fatal Myocardial Infarction (MI) Non-fatal Cerebral Infarction (CI) except for transient ischemic attack (TIA) Unstable angina requiring urgent hospitalizations

Time frame: 4-year

Secondary Outcomes

Composite cardiovascular events

Occurrence of one of following events: Cardiovascular death Non-fatal MI Non-fatal CI Unstable angina requiring hospitalizations Ischemia-driven coronary revascularization except target lesion revascularization (TLR)

Time frame: 4-year

Composite coronary heart disease events

Occurrence of one of following events: Coronary heart disease (CHD) death Non-fatal MI Unstable angina requiring urgent hospitalizations Ischemia-driven coronary revascularization except TLR

Time frame: 4-year

Composite cerebrovascular events

Occurrence of one of following events: Fatal and Non-fatal stroke Transient ischemic attack requiring hospitalizations

Time frame: 4-year

Mortality

Occurrence of each following events: All-cause mortality Cardiovascular death Cardiac death (death from coronary disease or heart failure or arrhythmia and sudden death) CHD death (death from myocardial infarction and sudden death)

Time frame: 4-year

Heart disease events

Occurrence of each following events: Fatal and Non-fatal MI Non-procedure related MI Procedure related MI Unstable angina requiring urgent hospitalizations Resuscitated cardiac arrest Hospitalization for heart failure PCI or CABG 1. All events of PCI or CABG 1. TLR 2. non-TLR 2. Ischemia-driven PCI or CABG 1. TLR 2. non-TLR

Time frame: 4-year

Cerebrovascular events

Occurrence of each following events: Fatal and Non-fatal stroke Fatal and Non-fatal CI 1. Non-procedure related CI 2. Procedure related CI Fatal and Non-fatal cerebral hemorrhage Hospitalization for TIA

Time frame: 4-year

Other events

Occurrence of each following events: Operation for or rupture of aortic aneurysm Revascularization for peripheral arterial disease (PAD) Carotid artery stenting (CAS) or carotid endarterectomy (CEA) Aortic dissection Deep vein thrombosis (DVT) or pulmonary thromboembolism (PTE) New occurrence of malignant tumor Operation for aortic stenosis

Time frame: 4-year

Extended Japan Assessment of Pitavastatin and Atorvastatin in Acute Coronary Syndrome

Overview

Conditions

Eligibility

Locations (2)

Outcomes

Primary Outcomes

Secondary Outcomes