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Plasma carotenoids, vitamin C, tocopherols, and retinol and the risk of breast cancer in the European Prospective Investigation into Cancer and Nutrition cohort

Authors :
Bakker, Marije F. Peeters, Petra H. M. Klaasen, Veronique M. and Bueno-de-Mesquita, H. Bas Jansen, Eugene H. J. M. Ros, Martine M. Travier, Noemie Olsen, Anja Tjonneland, Anne Overvad, Kim Rinaldi, Sabina Romieu, Isabelle Brennan, Paul and Boutron-Ruault, Marie-Christine Perquier, Florence Cadeau, Claire Boeing, Heiner Aleksandrova, Krasimira Kaaks, Rudolf and Kuehn, Tilman Trichopoulou, Antonia Lagiou, Pagona and Trichopoulos, Dimitrios Vineis, Paolo Krogh, Vittorio and Panico, Salvatore Masala, Giovanna Tumino, Rosario and Weiderpass, Elisabete Skeie, Guri Lund, Eiliv Ramon Quiros, J. Ardanaz, Eva Navarro, Carmen Amiano, Pilar Sanchez, Maria-Jose Buckland, Genevieve Ericson, Ulrika Sonestedt, Emily Johansson, Matthias Sund, Malin Travis, Ruth C. and Key, Timothy J. Khaw, Kay-Tee Wareham, Nick Riboli, Elio and van Gils, Carla H.
Publication Year :
2016

Abstract

Background: Carotenoids and vitamin C are thought to be associated with reduced cancer risk because of their antioxidative capacity. Objective: This study evaluated the associations of plasma carotenoid, retinol, tocopherol, and vitamin C concentrations and risk of breast cancer. Design: In a nested case-control study within the European Prospective Investigation into Cancer and Nutrition cohort, 1502 female incident breast cancer cases were included, with an oversampling of premenopausal (n = 582) and estrogen receptor-negative (ER-) cases (n = 462). Controls (n = 1502) were individually matched to cases by using incidence density sampling. Prediagnostic samples were analyzed for alpha-carotene, beta-carotene, lycopene, lutein, zeaxanthin, beta-cryptoxanthin, retinol, alpha-tocopherol, gamma-tocopherol, and 454 vitamin C. Breast cancer risk was computed according to hormone receptor status and age at diagnosis (proxy for menopausal status) by using conditional logistic regression and was further stratified by smoking status, alcohol consumption, and body mass index (BMI). All statistical tests were 2-sided. Results: In quintile 5 compared with quintile 1, alpha-carotene (OR: 0.61; 95% CI: 0.39, 0.98) and beta-carotene (OR: 0.41; 95% CI: 0.26, 0.65) were inversely associated with risk of ER- breast tumors. The other analytes were not statistically associated with ER- breast cancer. For estrogen receptor-positive (ER+) tumors, no statistically significant associations were found. The test for heterogeneity between ER- and ER+ tumors was statistically significant only for beta-carotene (P-heterogeneity = 0.03). A higher risk of breast cancer was found for retinol in relation to ER-/progesterone receptor-negative tumors (OR: 2.37; 95% CI: 1.20, 4.67; P-heterogeneity with ER+/progesterone receptor positive = 0.06). We observed no statistically significant interaction between smoking, alcohol, or BMI and all investigated plasma analytes (based on tertile distribution). Conclusion: Our results indicate that higher concentrations of plasma beta-carotene and alpha-carotene are associated with lower breast cancer risk of ER tumors.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.od......2127..ab93ae9c6ca5d984c6171d6c1cbf4aa5