Complemed.Com, Inc.

The Alternative Network And Information Resource.

Get your personalized e-mail

MedMail -- The E-mail Service for the Medical Community

 

.
.
wpe13.jpg (4074 bytes)

Last Updated
September 14, 1999

 

corner
Home

Acupuncture&TCM

Herbal Medicine

Homeopathy

Nutrition

Mens Health

Womens Health

Vitamins

 

Bernd2.jpg (9970 bytes)

 

Bernd Wollschlaeger,M.D.   CEO&Medical Director Click here for E-mail

 

Advisory Board

Steve Chasens, A.P.   Click here for E-Mail

Paul Cooley, LMT    Click here for E-Mail

.

 

Cambridge Heart Antioxidant Study (CHAOS)

 

Title
Randomised controlled trial of vitamin E in patients with coronary disease: Cambridge Heart Antioxidant Study (CHAOS) [see comments]
Author
Stephens NG; Parsons A; Schofield PM; Kelly F; Cheeseman K; Mitchinson MJ
Address
Department of Medicine, Cambridge University.
Source
Lancet, 347(9004):781-6 1996 Mar 23
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.
Language
Eng
Unique Identifier
96180130
MESH Headings
Comparative Study ; Coronary Arteriosclerosis MO/*PC ; Dose-Response Relationship, Drug ; Double-Blind Method ; Female ; Follow-Up Studies ; Human ; Lipid Peroxidation DE ; Male ; Middle Age ; Myocardial Infarction MO/PC ; Prospective Studies ; Risk Factors ; Survival Analysis ; Time Factors ; Vitamin E AD/*TU

©1998-1999 Complemed, Inc. All rights reserved. All information is intended for your general knowledge only and is not a substitute for medical advice or treatment for specific medical conditions. You should seek prompt medical care for any specific health issues and consult your physician before starting a new treatment regimen. Use of this online service is subject to the disclaimer and the terms and conditions .