Authors |
Lonn
E, Yusuf S, Arnold MJ, Sheridan P, Pogue J, Micks M, McQueen MJ, Probstfield
J, Fodor G, Held C, Genest J Jr; Heart Outcomes Prevention Evaluation
(HOPE) 2 Investigators.
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Abstract |
BACKGROUND:
In observational studies, lower homocysteine levels are associated with
lower rates of coronary heart disease and stroke. Folic acid and vitamins
B6 and B12 lower homocysteine levels. We assessed whether supplementation
reduced the risk of major cardiovascular events in patients with vascular
disease.
METHODS: We randomly assigned 5522 patients 55 years of age or older who
had vascular disease or diabetes to daily treatment either with the combination
of 2.5 mg of folic acid, 50 mg of vitamin B6, and 1 mg of vitamin B12
or with placebo for an average of five years. The primary outcome was
a composite of death from cardiovascular causes, myocardial infarction,
and stroke.
RESULTS:
Mean plasma homocysteine levels decreased by 2.4 micromol per liter (0.3
mg per liter) in the active-treatment group and increased by 0.8 micromol
per liter (0.1 mg per liter) in the placebo group. Primary outcome events
occurred in 519 patients (18.8 percent) assigned to active therapy and
547 (19.8 percent) assigned to placebo (relative risk, 0.95; 95 percent
confidence interval, 0.84 to 1.07; P=0.41). As compared with placebo,
active treatment did not significantly decrease the risk of death from
cardiovascular causes (relative risk, 0.96; 95 percent confidence interval,
0.81 to 1.13), myocardial infarction (relative risk, 0.98; 95 percent
confidence interval, 0.85 to 1.14), or any of the secondary outcomes.
Fewer patients assigned to active treatment than to placebo had a stroke
(relative risk, 0.75; 95 percent confidence interval, 0.59 to 0.97). More
patients in the active-treatment group were hospitalized for unstable
angina (relative risk, 1.24; 95 percent confidence interval, 1.04 to 1.49).
CONCLUSIONS: Supplements combining folic acid and vitamins B6 and B12
did not reduce the risk of major cardiovascular events in patients with
vascular disease. (ClinicalTrials.gov number, NCT00106886; Current Controlled
Trials number, ISRCTN14017017).
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