TY - JOUR
T1 - Genetically predicted circulating concentrations of micronutrients and risk of colorectal cancer among individuals of European descent
T2 - A Mendelian randomization study
AU - GECCO, CORECT, and CCFR
AU - Tsilidis, Konstantinos K.
AU - Papadimitriou, Nikos
AU - Dimou, Niki
AU - Gill, Dipender
AU - Lewis, Sarah J.
AU - Martin, Richard M.
AU - Murphy, Neil
AU - Markozannes, Georgios
AU - Zuber, Verena
AU - Cross, Amanda J.
AU - Burrows, Kimberley
AU - Lopez, David S.
AU - Key, Timothy J.
AU - Travis, Ruth C.
AU - Perez-Cornago, Aurora
AU - Hunter, David J.
AU - Van Duijnhoven, Fränzel J.B.
AU - Albanes, Demetrius
AU - Arndt, Volker
AU - Berndt, Sonja I.
AU - Bézieau, Stéphane
AU - Bishop, D. Timothy
AU - Boehm, Juergen
AU - Brenner, Hermann
AU - Burnett-Hartman, Andrea
AU - Campbell, Peter T.
AU - Casey, Graham
AU - Castellví-Bel, Sergi
AU - Chan, Andrew T.
AU - Chang-Claude, Jenny
AU - De La Chapelle, Albert
AU - Figueiredo, Jane C.
AU - Gallinger, Steven J.
AU - Giles, Graham G.
AU - Goodman, Phyllis J.
AU - Gsur, Andrea
AU - Hampe, Jochen
AU - Hampel, Heather
AU - Hoffmeister, Michael
AU - Jenkins, Mark A.
AU - Keku, Temitope O.
AU - Kweon, Sun Seog
AU - Larsson, Susanna C.
AU - Le Marchand, Loic
AU - Li, Christopher I.
AU - Li, Li
AU - Lindblom, Annika
AU - Martín, Vicente
AU - Milne, Roger L.
AU - Moreno, Victor
N1 - Publisher Copyright:
© 2021 The Author(s). Published by Oxford University Press on behalf of the American Society for Nutrition.
PY - 2021/6/1
Y1 - 2021/6/1
N2 - Background: The literature on associations of circulating concentrations of minerals and vitamins with risk of colorectal cancer is limited and inconsistent. Evidence from randomized controlled trials (RCTs) to support the efficacy of dietary modification or nutrient supplementation for colorectal cancer prevention is also limited. Objectives: To complement observational and RCT findings, we investigated associations of genetically predicted concentrations of 11 micronutrients (β-carotene, calcium, copper, folate, iron, magnesium, phosphorus, selenium, vitamin B-6, vitamin B-12, and zinc) with colorectal cancer risk using Mendelian randomization (MR). Methods: Two-sample MR was conducted using 58,221 individuals with colorectal cancer and 67,694 controls from the Genetics and Epidemiology of Colorectal Cancer Consortium, Colorectal Cancer Transdisciplinary Study, and Colon Cancer Family Registry. Inverse variance-weighted MR analyses were performed with sensitivity analyses to assess the impact of potential violations of MR assumptions. Results: Nominally significant associations were noted for genetically predicted iron concentration and higher risk of colon cancer [ORs per SD (ORSD): 1.08 95% CI: 1.00, 1.17 P value = 0.05] and similarly for proximal colon cancer, and for vitamin B-12 concentration and higher risk of colorectal cancer (ORSD: 1.12 95% CI: 1.03, 1.21 P value = 0.01) and similarly for colon cancer. A nominally significant association was also noted for genetically predicted selenium concentration and lower risk of colon cancer (ORSD: 0.98 95% CI: 0.96, 1.00 P value = 0.05) and similarly for distal colon cancer. These associations were robust to sensitivity analyses. Nominally significant inverse associations were observed for zinc and risk of colorectal and distal colon cancers, but sensitivity analyses could not be performed. None of these findings survived correction for multiple testing. Genetically predicted concentrations of β-carotene, calcium, copper, folate, magnesium, phosphorus, and vitamin B-6 were not associated with disease risk. Conclusions: These results suggest possible causal associations of circulating iron and vitamin B-12 (positively) and selenium (inversely) with risk of colon cancer.
AB - Background: The literature on associations of circulating concentrations of minerals and vitamins with risk of colorectal cancer is limited and inconsistent. Evidence from randomized controlled trials (RCTs) to support the efficacy of dietary modification or nutrient supplementation for colorectal cancer prevention is also limited. Objectives: To complement observational and RCT findings, we investigated associations of genetically predicted concentrations of 11 micronutrients (β-carotene, calcium, copper, folate, iron, magnesium, phosphorus, selenium, vitamin B-6, vitamin B-12, and zinc) with colorectal cancer risk using Mendelian randomization (MR). Methods: Two-sample MR was conducted using 58,221 individuals with colorectal cancer and 67,694 controls from the Genetics and Epidemiology of Colorectal Cancer Consortium, Colorectal Cancer Transdisciplinary Study, and Colon Cancer Family Registry. Inverse variance-weighted MR analyses were performed with sensitivity analyses to assess the impact of potential violations of MR assumptions. Results: Nominally significant associations were noted for genetically predicted iron concentration and higher risk of colon cancer [ORs per SD (ORSD): 1.08 95% CI: 1.00, 1.17 P value = 0.05] and similarly for proximal colon cancer, and for vitamin B-12 concentration and higher risk of colorectal cancer (ORSD: 1.12 95% CI: 1.03, 1.21 P value = 0.01) and similarly for colon cancer. A nominally significant association was also noted for genetically predicted selenium concentration and lower risk of colon cancer (ORSD: 0.98 95% CI: 0.96, 1.00 P value = 0.05) and similarly for distal colon cancer. These associations were robust to sensitivity analyses. Nominally significant inverse associations were observed for zinc and risk of colorectal and distal colon cancers, but sensitivity analyses could not be performed. None of these findings survived correction for multiple testing. Genetically predicted concentrations of β-carotene, calcium, copper, folate, magnesium, phosphorus, and vitamin B-6 were not associated with disease risk. Conclusions: These results suggest possible causal associations of circulating iron and vitamin B-12 (positively) and selenium (inversely) with risk of colon cancer.
KW - Mendelian randomization
KW - colorectal cancer
KW - genes
KW - nutrition
KW - supplements
UR - http://www.scopus.com/inward/record.url?scp=85107390465&partnerID=8YFLogxK
U2 - 10.1093/ajcn/nqab003
DO - 10.1093/ajcn/nqab003
M3 - Article
C2 - 33740060
AN - SCOPUS:85107390465
SN - 0002-9165
VL - 113
SP - 1490
EP - 1502
JO - American Journal of Clinical Nutrition
JF - American Journal of Clinical Nutrition
IS - 6
ER -