Urinary level of 1,N6-ethenodeoxyadenosine, a marker of oxidative stress, is associated with salt excretion and ω6-polyunsaturated fatty acid intake in postmenopausal Japanese women

被引:31
作者
Hanaoka, T [1 ]
Nair, J
Takahashi, Y
Sasaki, S
Bartsch, H
Tsugane, S
机构
[1] Natl Canc Ctr, Res Inst E, Epidemiol & Biostat Div, Kashiwa, Chiba 2778577, Japan
[2] German Canc Res Ctr, Div Toxicol & Canc Risk Factors, D-6900 Heidelberg, Germany
关键词
etheno DNA adducts; urinary excretion; salt; polyunsaturated fatty acids; diet; cancer;
D O I
10.1002/ijc.10437
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Excretion of I,N-6-ethenodeoxyadenosine (epsilondA), a marker for lipid peroxidation (LPO)-derived DNA damage was analyzed in urine of nonsmoking postmenopausal women participating in a dietary intervention trial in Northern Japan. Hereby the efficacy of dietary consultation in reducing salt and increasing vitamin C and carotenes during I year was estimated. Thirty postmenopausal women, 60-69 years of age, from the intervention group and 30 age-matched women from the control group were randomly selected. The subjects completed a self-administered diet history questionnaire and in the pre- and post-intervention period 48 hr urine and fasting blood samples were collected. epsilondA in urine was analyzed by an immuno-precipitation-high performance liquid chromatography-fluorescence detection method. epsilondA excretion (/48 hr) in the 59 postmenopausal Japanese women with complete urine collection ranged from 12-226 pmol at the pre-intervention. At the pre-intervention, epsilondA excretion was positively associated with urinary salt excretion (R = 0.33, p = 0.01) and omega-6 polyunsaturated fatty acid intake (%energy value, R = 0.28, p = 0.03) in the 59 women. The average epsilondA excretion in the intervention group was 61 pmol at pre-intervention and 44 pmol at post-intervention (p = 0.14). In the control group, it was 58 pmol at pre-intervention and 75 pmol at post-intervention (p = 0.24). During the intervention period, 18129 (62%) of the subjects in the intervention group exhibited the decreased excretion and 10/26 (38%) in the control group (p = 0.08). Results from this pilot study suggest urinary epsilondA as a potential biomarker of DNA damage possibly derived from salt-induced inflammation and LPO; further exploration Of epsilondA in human biomonitoring studies is warranted. (C) 2002 Wiley-Liss, Inc.
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页码:71 / 75
页数:5
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