Harvard
Rudolph, A, Song, M, Brook, MN, Milne, RL, Mavaddat, N, Michailidou, K, Bolla, MK, Wang, Q, Dennis, J, Wilcox, AN, Hopper, JL, Southey, MC, Keeman, R, Fasching, PA, Beckmann, MW, Gago-Dominguez, M, Castelao, JE, Guénel, P, Truong, T
, Bojesen, SE, Flyger, H, Brenner, H, Arndt, V, Brauch, H, Brüning, T, Mannermaa, A, Kosma, V-M, Lambrechts, D, Keupers, M, Couch, FJ, Vachon, C, Giles, GG, MacInnis, RJ, Figueroa, J, Brinton, L, Czene, K, Brand, JS, Gabrielson, M, Humphreys, K, Cox, A, Cross, SS, Dunning, AM, Orr, N, Swerdlow, A, Hall, P, Pharoah, PDP, Schmidt, MK, Easton, DF, Chatterjee, N, Chang-Claude, J & García-Closas, M 2018, '
Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium'
International Journal of Epidemiology, vol. 47, no. 2, pp. 526-536.
https://doi.org/10.1093/ije/dyx242APA
Rudolph, A., Song, M., Brook, M. N., Milne, R. L., Mavaddat, N., Michailidou, K., ... García-Closas, M. (2018).
Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium.
International Journal of Epidemiology,
47(2), 526-536.
https://doi.org/10.1093/ije/dyx242CBE
Rudolph A, Song M, Brook MN, Milne RL, Mavaddat N, Michailidou K, Bolla MK, Wang Q, Dennis J, Wilcox AN, Hopper JL, Southey MC, Keeman R, Fasching PA, Beckmann MW, Gago-Dominguez M, Castelao JE, Guénel P, Truong T
, Bojesen SE, Flyger H, Brenner H, Arndt V, Brauch H, Brüning T, Mannermaa A, Kosma V-M, Lambrechts D, Keupers M, Couch FJ, Vachon C, Giles GG, MacInnis RJ, Figueroa J, Brinton L, Czene K, Brand JS, Gabrielson M, Humphreys K, Cox A, Cross SS, Dunning AM, Orr N, Swerdlow A, Hall P, Pharoah PDP, Schmidt MK, Easton DF, Chatterjee N, Chang-Claude J, García-Closas M. 2018.
Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium.
International Journal of Epidemiology. 47(2):526-536.
https://doi.org/10.1093/ije/dyx242MLA
Vancouver
Author
Rudolph, Anja ; Song, Minsun ; Brook, Mark N ; Milne, Roger L ; Mavaddat, Nasim ; Michailidou, Kyriaki ; Bolla, Manjeet K ; Wang, Qin ; Dennis, Joe ; Wilcox, Amber N ; Hopper, John L ; Southey, Melissa C ; Keeman, Renske ; Fasching, Peter A ; Beckmann, Matthias W ; Gago-Dominguez, Manuela ; Castelao, Jose E ; Guénel, Pascal ; Truong, Thérèse
; Bojesen, Stig E ; Flyger, Henrik ; Brenner, Hermann ; Arndt, Volker ; Brauch, Hiltrud ; Brüning, Thomas ; Mannermaa, Arto ; Kosma, Veli-Matti ; Lambrechts, Diether ; Keupers, Machteld ; Couch, Fergus J ; Vachon, Celine ; Giles, Graham G ; MacInnis, Robert J ; Figueroa, Jonine ; Brinton, Louise ; Czene, Kamila ; Brand, Judith S ; Gabrielson, Marike ; Humphreys, Keith ; Cox, Angela ; Cross, Simon S ; Dunning, Alison M ; Orr, Nick ; Swerdlow, Anthony ; Hall, Per ; Pharoah, Paul D P ; Schmidt, Marjanka K ; Easton, Douglas F ; Chatterjee, Nilanjan ; Chang-Claude, Jenny ; García-Closas, Montserrat. /
Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium. In:
International Journal of Epidemiology. 2018 ; Vol. 47, No. 2. pp. 526-536.
Bibtex
@article{ce1a00ea922149538f344b534186192c,
title = "Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium",
abstract = "Background: Polygenic risk scores (PRS) for breast cancer can be used to stratify the population into groups at substantially different levels of risk. Combining PRS and environmental risk factors will improve risk prediction; however, integrating PRS into risk prediction models requires evaluation of their joint association with known environmental risk factors.Methods: Analyses were based on data from 20 studies; datasets analysed ranged from 3453 to 23 104 invasive breast cancer cases and similar numbers of controls, depending on the analysed environmental risk factor. We evaluated joint associations of a 77-single nucleotide polymorphism (SNP) PRS with reproductive history, alcohol consumption, menopausal hormone therapy (MHT), height and body mass index (BMI). We tested the null hypothesis of multiplicative joint associations for PRS and each of the environmental factors, and performed global and tail-based goodness-of-fit tests in logistic regression models. The outcomes were breast cancer overall and by estrogen receptor (ER) status.Results: The strongest evidence for a non-multiplicative joint associations with the 77-SNP PRS was for alcohol consumption (P-interaction = 0.009), adult height (P-interaction = 0.025) and current use of combined MHT (P-interaction = 0.038) in ER-positive disease. Risk associations for these factors by percentiles of PRS did not follow a clear dose-response. In addition, global and tail-based goodness of fit tests showed little evidence for departures from a multiplicative risk model, with alcohol consumption showing the strongest evidence for ER-positive disease (P = 0.013 for global and 0.18 for tail-based tests).Conclusions: The combined effects of the 77-SNP PRS and environmental risk factors for breast cancer are generally well described by a multiplicative model. Larger studies are required to confirm possible departures from the multiplicative model for individual risk factors, and assess models specific for ER-negative disease.",
author = "Anja Rudolph and Minsun Song and Brook, {Mark N} and Milne, {Roger L} and Nasim Mavaddat and Kyriaki Michailidou and Bolla, {Manjeet K} and Qin Wang and Joe Dennis and Wilcox, {Amber N} and Hopper, {John L} and Southey, {Melissa C} and Renske Keeman and Fasching, {Peter A} and Beckmann, {Matthias W} and Manuela Gago-Dominguez and Castelao, {Jose E} and Pascal Gu{\'e}nel and Th{\'e}r{\`e}se Truong and Bojesen, {Stig E} and Henrik Flyger and Hermann Brenner and Volker Arndt and Hiltrud Brauch and Thomas Br{\"u}ning and Arto Mannermaa and Veli-Matti Kosma and Diether Lambrechts and Machteld Keupers and Couch, {Fergus J} and Celine Vachon and Giles, {Graham G} and MacInnis, {Robert J} and Jonine Figueroa and Louise Brinton and Kamila Czene and Brand, {Judith S} and Marike Gabrielson and Keith Humphreys and Angela Cox and Cross, {Simon S} and Dunning, {Alison M} and Nick Orr and Anthony Swerdlow and Per Hall and Pharoah, {Paul D P} and Schmidt, {Marjanka K} and Easton, {Douglas F} and Nilanjan Chatterjee and Jenny Chang-Claude and Montserrat Garc{\'i}a-Closas",
year = "2018",
month = "4",
day = "1",
doi = "10.1093/ije/dyx242",
language = "English",
volume = "47",
pages = "526--536",
journal = "International Journal of Epidemiology",
issn = "0300-5771",
publisher = "Oxford University Press",
number = "2",
}
RIS
TY - JOUR
T1 - Joint associations of a polygenic risk score and environmental risk factors for breast cancer in the Breast Cancer Association Consortium
AU - Rudolph, Anja
AU - Song, Minsun
AU - Brook, Mark N
AU - Milne, Roger L
AU - Mavaddat, Nasim
AU - Michailidou, Kyriaki
AU - Bolla, Manjeet K
AU - Wang, Qin
AU - Dennis, Joe
AU - Wilcox, Amber N
AU - Hopper, John L
AU - Southey, Melissa C
AU - Keeman, Renske
AU - Fasching, Peter A
AU - Beckmann, Matthias W
AU - Gago-Dominguez, Manuela
AU - Castelao, Jose E
AU - Guénel, Pascal
AU - Truong, Thérèse
AU - Bojesen, Stig E
AU - Flyger, Henrik
AU - Brenner, Hermann
AU - Arndt, Volker
AU - Brauch, Hiltrud
AU - Brüning, Thomas
AU - Mannermaa, Arto
AU - Kosma, Veli-Matti
AU - Lambrechts, Diether
AU - Keupers, Machteld
AU - Couch, Fergus J
AU - Vachon, Celine
AU - Giles, Graham G
AU - MacInnis, Robert J
AU - Figueroa, Jonine
AU - Brinton, Louise
AU - Czene, Kamila
AU - Brand, Judith S
AU - Gabrielson, Marike
AU - Humphreys, Keith
AU - Cox, Angela
AU - Cross, Simon S
AU - Dunning, Alison M
AU - Orr, Nick
AU - Swerdlow, Anthony
AU - Hall, Per
AU - Pharoah, Paul D P
AU - Schmidt, Marjanka K
AU - Easton, Douglas F
AU - Chatterjee, Nilanjan
AU - Chang-Claude, Jenny
AU - García-Closas, Montserrat
PY - 2018/4/1
Y1 - 2018/4/1
N2 - Background: Polygenic risk scores (PRS) for breast cancer can be used to stratify the population into groups at substantially different levels of risk. Combining PRS and environmental risk factors will improve risk prediction; however, integrating PRS into risk prediction models requires evaluation of their joint association with known environmental risk factors.Methods: Analyses were based on data from 20 studies; datasets analysed ranged from 3453 to 23 104 invasive breast cancer cases and similar numbers of controls, depending on the analysed environmental risk factor. We evaluated joint associations of a 77-single nucleotide polymorphism (SNP) PRS with reproductive history, alcohol consumption, menopausal hormone therapy (MHT), height and body mass index (BMI). We tested the null hypothesis of multiplicative joint associations for PRS and each of the environmental factors, and performed global and tail-based goodness-of-fit tests in logistic regression models. The outcomes were breast cancer overall and by estrogen receptor (ER) status.Results: The strongest evidence for a non-multiplicative joint associations with the 77-SNP PRS was for alcohol consumption (P-interaction = 0.009), adult height (P-interaction = 0.025) and current use of combined MHT (P-interaction = 0.038) in ER-positive disease. Risk associations for these factors by percentiles of PRS did not follow a clear dose-response. In addition, global and tail-based goodness of fit tests showed little evidence for departures from a multiplicative risk model, with alcohol consumption showing the strongest evidence for ER-positive disease (P = 0.013 for global and 0.18 for tail-based tests).Conclusions: The combined effects of the 77-SNP PRS and environmental risk factors for breast cancer are generally well described by a multiplicative model. Larger studies are required to confirm possible departures from the multiplicative model for individual risk factors, and assess models specific for ER-negative disease.
AB - Background: Polygenic risk scores (PRS) for breast cancer can be used to stratify the population into groups at substantially different levels of risk. Combining PRS and environmental risk factors will improve risk prediction; however, integrating PRS into risk prediction models requires evaluation of their joint association with known environmental risk factors.Methods: Analyses were based on data from 20 studies; datasets analysed ranged from 3453 to 23 104 invasive breast cancer cases and similar numbers of controls, depending on the analysed environmental risk factor. We evaluated joint associations of a 77-single nucleotide polymorphism (SNP) PRS with reproductive history, alcohol consumption, menopausal hormone therapy (MHT), height and body mass index (BMI). We tested the null hypothesis of multiplicative joint associations for PRS and each of the environmental factors, and performed global and tail-based goodness-of-fit tests in logistic regression models. The outcomes were breast cancer overall and by estrogen receptor (ER) status.Results: The strongest evidence for a non-multiplicative joint associations with the 77-SNP PRS was for alcohol consumption (P-interaction = 0.009), adult height (P-interaction = 0.025) and current use of combined MHT (P-interaction = 0.038) in ER-positive disease. Risk associations for these factors by percentiles of PRS did not follow a clear dose-response. In addition, global and tail-based goodness of fit tests showed little evidence for departures from a multiplicative risk model, with alcohol consumption showing the strongest evidence for ER-positive disease (P = 0.013 for global and 0.18 for tail-based tests).Conclusions: The combined effects of the 77-SNP PRS and environmental risk factors for breast cancer are generally well described by a multiplicative model. Larger studies are required to confirm possible departures from the multiplicative model for individual risk factors, and assess models specific for ER-negative disease.
U2 - 10.1093/ije/dyx242
DO - 10.1093/ije/dyx242
M3 - Journal article
VL - 47
SP - 526
EP - 536
JO - International Journal of Epidemiology
JF - International Journal of Epidemiology
SN - 0300-5771
IS - 2
ER -
