Intensive lipid lowering with atorvastatin in patients with stable coronary disease
- PMID: 15755765
- DOI: 10.1056/NEJMoa050461
Intensive lipid lowering with atorvastatin in patients with stable coronary disease
Abstract
Background: Previous trials have demonstrated that lowering low-density lipoprotein (LDL) cholesterol levels below currently recommended levels is beneficial in patients with acute coronary syndromes. We prospectively assessed the efficacy and safety of lowering LDL cholesterol levels below 100 mg per deciliter (2.6 mmol per liter) in patients with stable coronary heart disease (CHD).
Methods: A total of 10,001 patients with clinically evident CHD and LDL cholesterol levels of less than 130 mg per deciliter (3.4 mmol per liter) were randomly assigned to double-blind therapy and received either 10 mg or 80 mg of atorvastatin per day. Patients were followed for a median of 4.9 years. The primary end point was the occurrence of a first major cardiovascular event, defined as death from CHD, nonfatal non-procedure-related myocardial infarction, resuscitation after cardiac arrest, or fatal or nonfatal stroke.
Results: The mean LDL cholesterol levels were 77 mg per deciliter (2.0 mmol per liter) during treatment with 80 mg of atorvastatin and 101 mg per deciliter (2.6 mmol per liter) during treatment with 10 mg of atorvastatin. The incidence of persistent elevations in liver aminotransferase levels was 0.2 percent in the group given 10 mg of atorvastatin and 1.2 percent in the group given 80 mg of atorvastatin (P<0.001). A primary event occurred in 434 patients (8.7 percent) receiving 80 mg of atorvastatin, as compared with 548 patients (10.9 percent) receiving 10 mg of atorvastatin, representing an absolute reduction in the rate of major cardiovascular events of 2.2 percent and a 22 percent relative reduction in risk (hazard ratio, 0.78; 95 percent confidence interval, 0.69 to 0.89; P<0.001). There was no difference between the two treatment groups in overall mortality.
Conclusions: Intensive lipid-lowering therapy with 80 mg of atorvastatin per day in patients with stable CHD provides significant clinical benefit beyond that afforded by treatment with 10 mg of atorvastatin per day. This occurred with a greater incidence of elevated aminotransferase levels.
Copyright 2005 Massachusetts Medical Society.
Comment in
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Low-density lipoprotein cholesterol in patients with stable coronary heart disease--is it time to shift our goals?N Engl J Med. 2005 Apr 7;352(14):1483-4. doi: 10.1056/NEJMe058052. Epub 2005 Mar 8. N Engl J Med. 2005. PMID: 15755764 No abstract available.
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Intensive lipid lowering with atorvastatin in coronary disease.N Engl J Med. 2005 Jul 7;353(1):93-6; author reply 93-6. doi: 10.1056/NEJM200507073530117. N Engl J Med. 2005. PMID: 16000362 No abstract available.
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Intensive lipid lowering with atorvastatin in coronary disease.N Engl J Med. 2005 Jul 7;353(1):93-6; author reply 93-6. N Engl J Med. 2005. PMID: 16003831 No abstract available.
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Intensive lipid lowering with atorvastatin in coronary disease.N Engl J Med. 2005 Jul 7;353(1):93-6; author reply 93-6. N Engl J Med. 2005. PMID: 16003832 No abstract available.
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Intensive lipid lowering with atorvastatin in coronary disease.N Engl J Med. 2005 Jul 7;353(1):93-6; author reply 93-6. N Engl J Med. 2005. PMID: 16003833 No abstract available.
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Intensive lipid lowering with atorvastatin in coronary disease.N Engl J Med. 2005 Jul 7;353(1):93-6; author reply 93-6. N Engl J Med. 2005. PMID: 16003834 No abstract available.
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Women's health study (aspirin) and TNT.Prev Cardiol. 2005 Summer;8(3):181-5. doi: 10.1111/j.1520-037x.2005.4010.x. Prev Cardiol. 2005. PMID: 16034223 No abstract available.
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Atorvastatin at 80 mg/d reduced major cardiovascular events more than atorvastatin at 10 mg/d in stable coronary heart disease.ACP J Club. 2005 Sep-Oct;143(2):38. ACP J Club. 2005. PMID: 16134912 No abstract available.
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Statin therapy after stroke or transient ischemic attack.N Engl J Med. 2006 Nov 30;355(22):2368; author reply 2370-1. doi: 10.1056/NEJMc062456. N Engl J Med. 2006. PMID: 17135593 No abstract available.
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