TY - JOUR
T1 - Circulating Vitamin D concentrations and risk of breast and prostate cancer
T2 - A Mendelian randomization study
AU - Jiang, Xia
AU - Dimou, Niki L.
AU - Al-Dabhani, Kawthar
AU - Lewis, Sarah J.
AU - Martin, Richard M.
AU - Haycock, Philip C.
AU - Gunter, Marc J.
AU - Key, Timothy J.
AU - Eeles, Rosalind A.
AU - Muir, Kenneth
AU - Neal, David
AU - Giles, Graham G.
AU - Giovannucci, Edward L.
AU - Stampfer, Meir
AU - Pierce, Brandon L.
AU - Schildkraut, Joellen M.
AU - Andersen, Shaneda Warren
AU - Thompson, Deborah
AU - Zheng, Wei
AU - Kraft, Peter
AU - Tsilidis, Konstantinos K.
N1 - Publisher Copyright:
© The Author(s) 2018; all rights reserved.
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Background: Observational studies have suggested an association between circulating vitamin D concentrations [25(OH)D] and risk of breast and prostate cancer, which was not supported by a recent Mendelian randomization (MR) analysis comprising 15 748 breast and 22 898 prostate-cancer cases. Demonstrating causality has proven challenging and one common limitation of MR studies is insufficient power. Methods: We aimed to determine whether circulating concentrations of vitamin D are causally associated with the risk of breast and prostate cancer, by using summary-level data from the largest ever genome-wide association studies conducted on vitamin D (N=73 699), breast cancer (Ncase=122 977) and prostate cancer (Ncase=79 148). We constructed a stronger instrument using six common genetic variants (compared with the previous four variants) and applied several two-sample MR methods. Results: We found no evidence to support a causal association between 25(OH)D and risk of breast cancer [OR per 25 nmol/L increase, 1.02 (95% confidence interval: 0.97- 1.08), P=0.47], oestrogen receptor (ER)+ [1.00 (0.94-1.07), P=0.99] or ER+ [1.02 (0.90- 1.16), P=0.75] subsets, prostate cancer [1.00 (0.93-1.07), P=0.99] or the advanced subtype [1.02 (0.90-1.16), P=0.72] using the inverse-variance-weighted method. Sensitivity analyses did not reveal any sign of directional pleiotropy. Conclusions: Despite its almost five-fold augmented sample size and substantially improved statistical power, our MR analysis does not support a causal effect of circulating 25(OH)D concentrations on breast- or prostate-cancer risk. However, we can still not exclude a modest or non-linear effect of vitamin D. Future studies may be designed to understand the effect of vitamin D in subpopulations with a profound deficiency.
AB - Background: Observational studies have suggested an association between circulating vitamin D concentrations [25(OH)D] and risk of breast and prostate cancer, which was not supported by a recent Mendelian randomization (MR) analysis comprising 15 748 breast and 22 898 prostate-cancer cases. Demonstrating causality has proven challenging and one common limitation of MR studies is insufficient power. Methods: We aimed to determine whether circulating concentrations of vitamin D are causally associated with the risk of breast and prostate cancer, by using summary-level data from the largest ever genome-wide association studies conducted on vitamin D (N=73 699), breast cancer (Ncase=122 977) and prostate cancer (Ncase=79 148). We constructed a stronger instrument using six common genetic variants (compared with the previous four variants) and applied several two-sample MR methods. Results: We found no evidence to support a causal association between 25(OH)D and risk of breast cancer [OR per 25 nmol/L increase, 1.02 (95% confidence interval: 0.97- 1.08), P=0.47], oestrogen receptor (ER)+ [1.00 (0.94-1.07), P=0.99] or ER+ [1.02 (0.90- 1.16), P=0.75] subsets, prostate cancer [1.00 (0.93-1.07), P=0.99] or the advanced subtype [1.02 (0.90-1.16), P=0.72] using the inverse-variance-weighted method. Sensitivity analyses did not reveal any sign of directional pleiotropy. Conclusions: Despite its almost five-fold augmented sample size and substantially improved statistical power, our MR analysis does not support a causal effect of circulating 25(OH)D concentrations on breast- or prostate-cancer risk. However, we can still not exclude a modest or non-linear effect of vitamin D. Future studies may be designed to understand the effect of vitamin D in subpopulations with a profound deficiency.
KW - Breast
KW - Malignancy
KW - Mendelian randomization
KW - Prostate
KW - Serum Vitamin D concentrations
UR - http://www.scopus.com/inward/record.url?scp=85075101244&partnerID=8YFLogxK
U2 - 10.1093/ije/dyy284
DO - 10.1093/ije/dyy284
M3 - Artículo
C2 - 30597039
AN - SCOPUS:85075101244
SN - 0300-5771
VL - 48
SP - 1416
EP - 1424
JO - International Journal of Epidemiology
JF - International Journal of Epidemiology
IS - 5
ER -