Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 1996 Mar 23;347(9004):781-6.
doi: 10.1016/s0140-6736(96)90866-1.

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

Affiliations
Clinical Trial

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

N G Stephens et al. Lancet. .

Abstract

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 micromol/L to 51.1 micromol/L with 400 IU daily and 64.5 micromol/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% Cl 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=0.005); however, there was a non-significant excess of cardiovascular deaths in the alpha-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.

PubMed Disclaimer

Comment in

  • ACP J Club. 1996 Jul-Aug;125(1):15
  • A fat little earner.
    [No authors listed] [No authors listed] Lancet. 1996 Mar 23;347(9004):775. Lancet. 1996. PMID: 8622326 No abstract available.
  • Coronary heart disease and vitamin E.
    Riemersma RA. Riemersma RA. Lancet. 1996 Mar 23;347(9004):776-7. doi: 10.1016/s0140-6736(96)90861-2. Lancet. 1996. PMID: 8622327 Clinical Trial. No abstract available.
  • Antioxidants and ischaemic heart disease.
    Violi F, Iuliano L. Violi F, et al. Lancet. 1997 Aug 30;350(9078):667-8. doi: 10.1016/s0140-6736(05)63364-8. Lancet. 1997. PMID: 9288075 No abstract available.
  • GISSI-Prevenzione trial.
    Jialal I, Devaraj S, Huet BA, Traber M. Jialal I, et al. Lancet. 1999 Oct 30;354(9189):1554; author reply 1556-7. doi: 10.1016/s0140-6736(99)90191-5. Lancet. 1999. PMID: 10551518 No abstract available.
  • GISSI-Prevenzione trial.
    Salen P, de Lorgeril M. Salen P, et al. Lancet. 1999 Oct 30;354(9189):1555; author reply 1556-7. doi: 10.1016/S0140-6736(05)76583-1. Lancet. 1999. PMID: 10551520 No abstract available.