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膳食硝酸盐和亚硝酸盐摄入与上海女性健康研究中的结直肠癌风险。

Dietary nitrate and nitrite intake and risk of colorectal cancer in the Shanghai Women's Health Study.

机构信息

Occupational and Environmental Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD.

出版信息

Int J Cancer. 2014 Jun 15;134(12):2917-26. doi: 10.1002/ijc.28612. Epub 2013 Nov 29.

Abstract

Nitrate and nitrite are precursors of endogenously formed N-nitroso compounds (NOC), known animal carcinogens. Nitrosation reactions forming NOCs can be inhibited by vitamin C and other antioxidants. We prospectively investigated the association between dietary nitrate and nitrite intake and risk of colorectal cancer in the Shanghai Women's Health Study, a cohort of 73,118 women ages 40-70 residing in Shanghai. We evaluated effect modification by factors that affect endogenous formation of NOCs: vitamin C (at or above/below median) and red meat intake (at or above/below median). Nitrate, nitrite and other dietary intakes were estimated from a 77-item food frequency questionnaire administered at baseline. Over a mean of 11 years of follow-up, we identified 619 colorectal cancer cases (n = 383, colon; n = 236, rectum). Hazard ratios (HR) and 95% confidence intervals (CI) were estimated using Cox proportional hazard regression. Overall, nitrate intake was not associated with colorectal cancer risk (HR = 1.08; 95% CI: 0.73-1.59). However, among women with vitamin C intake below the median (83.9 mg day(-1) ) and hence higher potential exposure to NOCs, risk of colorectal cancer increased with increasing quintiles of nitrate intake (highest vs. lowest quintile HR = 2.45; 95% CI: 1.15-5.18; p trend = 0.02). There was no association among women with higher vitamin C intake. We found no association between nitrite intake and risk of colorectal cancer overall or by intake level of vitamin C. Our findings suggest that high dietary nitrate intake among subgroups expected to have higher exposure to endogenously formed NOCs increases risk of colorectal cancer.

摘要

硝酸盐和亚硝酸盐是内源性形成的 N-亚硝基化合物(NOC)的前体,已知的动物致癌物。形成 NOC 的亚硝化反应可以被维生素 C 和其他抗氧化剂抑制。我们前瞻性地研究了膳食硝酸盐和亚硝酸盐摄入与上海妇女健康研究中结直肠癌风险的关系,该研究是一个居住在上海的 73118 名 40-70 岁女性的队列。我们评估了影响 NOC 内源性形成的因素(维生素 C(高于/低于中位数)和红肉摄入(高于/低于中位数)对效应的修饰作用。硝酸盐、亚硝酸盐和其他饮食摄入量是根据基线时进行的 77 项食物频率问卷评估的。在平均 11 年的随访期间,我们共确定了 619 例结直肠癌病例(n=383,结肠癌;n=236,直肠癌)。使用 Cox 比例风险回归估计风险比(HR)和 95%置信区间(CI)。总体而言,硝酸盐摄入量与结直肠癌风险无关(HR=1.08;95%CI:0.73-1.59)。然而,在维生素 C 摄入量低于中位数(83.9 毫克/天)且因此潜在暴露于 NOC 更高的女性中,随着硝酸盐摄入量五分位的增加,结直肠癌的风险增加(最高五分位与最低五分位 HR=2.45;95%CI:1.15-5.18;p 趋势=0.02)。在维生素 C 摄入量较高的女性中没有关联。我们没有发现亚硝酸盐摄入量与结直肠癌风险之间的总体关联或与维生素 C 摄入量水平的关联。我们的研究结果表明,在预期内源性形成 NOC 暴露较高的亚组中,高膳食硝酸盐摄入量会增加结直肠癌的风险。

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