Randomised controlled trial of vitamin E in patients with coronary disease: Cambridge Heart Antioxidant Study (CHAOS)

被引:1652
作者
Stephens, NG
Parsons, A
Schofield, PM
Kelly, F
Cheeseman, K
Mitchinson, MJ
Brown, MJ
机构
[1] UNIV CAMBRIDGE, DEPT MED, CLIN PHARMACOL UNIT, CAMBRIDGE, ENGLAND
[2] UNIV CAMBRIDGE, DEPT PATHOL, DIV CELLULAR PATHOL, CAMBRIDGE, ENGLAND
[3] PAPWORTH HOSP, CARDIAC UNIT, CAMBRIDGE, ENGLAND
[4] ST THOMAS HOSP, RAYNE INST, LONDON SE1 7EH, ENGLAND
[5] BRUNEL UNIV, DEPT BIOL & BIOCHEM, UXBRIDGE UB8 3PH, MIDDX, ENGLAND
关键词
D O I
10.1016/S0140-6736(96)90866-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Vitamin E (alpha-tocopherol) is thought to have a role in prevention of atherosclerosis, through inhibition of oxidation of low-density lipoprotein. Some epidemiological studies have shown an association between high dietary intake or high serum concentrations of alpha-tocopherol and lower rates of ischaemic heart disease. We tested the hypothesis that treatment with a high dose of alpha-tocopherol would reduce subsequent risk of myocardial infarction (MI) and cardiovascular death in patients with established ischaemic heart disease, Methods In this double-blind, placebo-controlled study with stratified randomisation, 2002 patients with angiographically proven coronary atherosclerosis were enrolled and followed up for a median of 510 days (range 3-981), 1035 patients were assigned alpha-tocopherol (capsules containing 800 IU daily for first 546 patients; 400 IU daily for remainder); 967 received identical placebo capsules. The primary endpoints were a combination of cardiovascular death and non-fatal MI as well as non-fatal MI alone. Findings Plasma alpha-tocopherol concentrations (measured in subsets of patients) rose in the actively treated group (from baseline mean 34.2 mu mol/L to 51.1 mu mol/L with 400 IU daily and 64.5 mu mol/L with 800 IU daily) but did not change in the placebo group. alpha-tocopherol treatment significantly reduced the risk of the primary trial endpoint of cardiovascular death and non-fatal MI (41 vs 64 events; relative risk 0.53 [95% CI 0.34-0.83; p=0.005). The beneficial effects on this composite endpoint were due to a significant reduction in the risk of non-fatal MI (14 vs 41; 0.23 [0.11-0.47]; p=0005); however, there was a nonsignificant excess of cardiovascular deaths in the cr-tocopherol group (27 vs 23; 1.18 [0.62-2.27]; p=0.61). All-cause mortality was 36 of 1035 alpha-tocopherol-treated patients and 27 of 967 placebo recipients. Interpretation We conclude that in patients with angiographically proven symptomatic coronary atherosclerosis, alpha-tocopherol treatment substantially reduces the rate of non-fatal-MI, with beneficial effects apparent after 1 year of treatment, The effect of alpha-tocopherol treatment on cardiovascular deaths requires further study.
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页码:781 / 786
页数:6
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