Dietary nitrate and nitrite intake and risk of colorectal cancer in the Shanghai Women's Health Study |
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Authors: | Curt T. DellaValle Qian Xiao Gong Yang Xiao-Ou Shu Briseis Aschebrook‐Kilfoy Wei Zheng Hong Lan Li Bu‐Tian Ji Nathaniel Rothman Wong‐Ho Chow Yu‐Tang Gao Mary H. Ward |
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Affiliation: | 1. 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;2. Nutritional Epidemiology Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD;3. Division of Epidemiology, Department of Medicine, Vanderbilt University, Nashville, TN;4. Vanderbilt Epidemiology Center and Vanderbilt‐Ingram Cancer Center, Department of Medicine, Vanderbilt University, Nashville, TN;5. Department of Health Studies, University of Chicago, Chicago, IL;6. Department of Epidemiology, Shanghai Cancer Institute, Shanghai, People's Republic of China;7. Department of Epidemiology, Division of OVP, Cancer Prevention and Population Sciences, The University of Texas MD Anderson Cancer Center, Houston, TX |
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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. |
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Keywords: | colon cancer rectum cancer nitrate nitrite vitamin C N‐nitroso compounds diet |
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