Background: Some experimental evidence suggests that iron may play a role in colorectal carcinogenesis, but human data for this role have been conflicting, possibly because of problems related to study design or measurement of iron exposure. We assessed dietary iron intake and genetic and biochemical markers of iron status in a prospective, nested case-control study of women enrolled in the Nurses' Health Study. Methods: Among 32826 women who provided a blood specimen, we identified 527 women with colorectal adenoma and 527 matched control subjects who underwent endoscopy but were not diagnosed with adenoma after blood collection. We assessed iron intake, mutations in the HFE gene that are associated with hereditary hemochromatosis (i.e., H63D and C282Y), and plasma biochemical measures of total body iron, including transferrin saturation and the ratio of the concentrations of transferrin receptors to ferritin. Logistic regression models were used to estimate relative risks (RR) and 95% confidence intervals (CI). All statistical tests were two-sided. Results: Women with any HFE gene mutation had higher total body iron stores, as reflected by higher transferrin saturations (P
CITATION STYLE
Chan, A. T., Ma, J., Tranah, G. J., Giovannucci, E. L., Rifai, N., Hunter, D. J., & Fuchs, C. S. (2005). Hemochromatosis gene mutations, body iron stores, dietary iron, and risk of colorectal adenoma in women. Journal of the National Cancer Institute, 97(12), 917–926. https://doi.org/10.1093/jnci/dji165
Mendeley helps you to discover research relevant for your work.