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a Department of
Therapeutics and Pharmacology, Queen's University of Belfast, Whitla
Medical Building, 97 Lisburn Rd, Belfast BT9 7BL, UK, b Department of Clinical Biochemistry, Queen's
University of Belfast
Correspondence to: Dr Hanratty c.hanratty{at}net.ntl.com
Accepted 25 October
2000
BACKGROUND
Raised homocysteine is a
risk factor for vascular disease. Homocysteine is formed from
methionine, and dietary manipulation of homocysteine in primates and
humans with oral methionine is associated with endothelial dysfunction.
A cause-effect relation has not been clearly established.
AIM
To study the effect of oral
methionine and then oral homocysteine on endothelial function.
METHODS
22 healthy adults were
recruited for two randomised crossover studies, each containing 11 subjects. Endothelial function was determined by measuring forearm
blood flow in response to intra-arterial infusion of acetylcholine
(endothelium dependent) and sodium nitroprusside (endothelium
independent). Subjects received methionine or placebo (study 1), or
homocysteine or placebo (study 2). Methionine and homocysteine were
determined at baseline and t = 4 hours. Endothelial function was
determined at four hours. The responses to the vasoactive substances
are expressed as the area under the curve of change in forearm blood
flow from baseline.
RESULTS
Study 1: plasma methionine
and homocysteine concentrations increased significantly versus placebo.
The increases were associated with a reduction of endothelium dependent
responses (mean (95% confidence interval), arbitrary units), from 48.8 (95% CI 36.4 to 61.2) to 29.9 (95% CI 18.0 to 41.1), p < 0.04;
endothelium independent responses were unchanged. Study 2: homocysteine
concentration increased significantly while methionine remained
unchanged. Endothelium dependent responses were reduced from 34.6 (95%
CI 20.6 to 48.6) to 22.8 (95% CI 12.0 to 33.6), p < 0.03.
CONCLUSIONS
Homocysteine and not
methionine is responsible for the changes in endothelial function. This
supports the hypothesis that homocysteine promotes atherosclerosis by
inducing endothelial dysfunction.
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