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Department of Epidemiology, School of Hygiene and Public Health [H-Y. H., K. J. H.], and Department of Medicine, School of Medicine [L. J. A.], Johns Hopkins University, Baltimore, Maryland 21205-2223
Oxidative DNA damage may be important in mutagenic, carcinogenic, and
aging processes. Although it is plausible that antioxidant vitamins may
reduce oxidative DNA damage, evidence from human studies has been
sparse and inconsistent. We determined the short-term effects of
vitamin C (500 mg/day) and vitamin E (400 IU
d-
- tocopheryl acetate/day) supplements on
oxidative DNA damage in a double-masked, placebo-controlled, 2x2
factorial trial in 184 nonsmoking adults. Mean duration of
supplementation was 2 months. Oxidative DNA damage was measured by 24-h
urinary excretion of 8-hydroxy-2'-deoxyguanosine (8-OHdG). At baseline,
urinary 8-OHdG (mean ± SE; ng/mg creatinine) was associated with
race (15.6 ± 0.8 in African Americans versus
20.3 ± 1.2 in Caucasians, P = 0.001), prior
antioxidant supplement use (18.6 ± 0.8 in users
versus 13.8 ± 1.5 in non-users,
P = 0.007), and regular exercise (19.2 ± 1.1
in exercisers versus 16.6 ± 0.9 in
non-exercisers, P = 0.04). Fruit and vegetable
intake and serum ascorbic acid were inversely associated with
urinary 8-OHdG (P-trend = 0.02 and 0.016,
respectively). The benefits of fruit and vegetable intake became
evident with the consumption being at least three servings/day. At the
end of supplementation, change from baseline in urinary 8-OHdG
(mean ± SE; ng/mg creatinine) was -0.6 ± 1.4
(P = 0.61), 0.6 ± 1.1 (P = 0.59), 0.5 ± 1.0 (P = 0.61), and 1.6 ± 1.4 (P = 0.27) in the placebo, vitamin C alone,
vitamin E alone, and combined vitamins C and E groups, respectively. In
overall and subgroup analyses, there was no significant main effect or
interaction effect of the supplements on urinary 8-OHdG. In conclusion,
supplementation of diet with vitamin C (500 mg/day) and vitamin E (400
IU d-
-tocopheryl acetate/day) had no significant main
effect or interaction effect on oxidative DNA damage as measured by
urinary 8-OHdG in nonsmoking adults. However, several aspects of a
healthy lifestyle were associated with lower oxidative DNA damage.
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